US Drug Watchdog Launches Now Calls Transvaginal Mesh A Disaster For 100,000's of US Women Recipients And Offers The Names and Contacts Of The Best Women Attorneys

Monday, June 18, 2012

The US Drug Watchdog says, "We are now calling the transvaginal mesh diaster the absolute worst mess we have ever seen for women, and the damages are literally beyond comprehension. We are also talking about a potentially huge number of US women. According to the New York Times, in 2010, about 185,000 women underwent procedures in which mesh was implanted vaginally to treat urinary incontinence. That is 2010 alone." Transvaginal mesh failure occurs when the mesh fails to bind to a woman's pelvic tissues. As a consequence of this, the body rejects the mesh that has been sewn into it. As a result, the transvaginal mesh may start to poke its way through the vaginal wall and protrude out of the vaginal tissue. This complication is more commonly referred to as "erosion." Erosion may result in extreme pain, infection, bleeding, vaginal discharge, with no possibility for sexual intercourse. The US Drug Watchdog has begun a very aggressive initiative designed to assist women in the United States, in what they are referring to as the Transvaginal Mesh Disaster. The group is urging any woman, who has had the transvaginal mesh surgical procedure done, and now has developed severe complications to call them anytime at 866-714-6466. As part of its initiative the US Drug Watchdog is offering to send all US women, who are victims of this Transvaginal Mesh Disaster to national caliber attorneys-who are all women. http://USDrugWatchdog.Com

(PRWEB) June 18, 2012

The US Drug Watchdog has now launched an aggressive national initiative designed to help women recipients of a transvaginal mesh, who are now severely damaged by this type of product. Supposedly the transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, and stress urinary incontinence. According to the US FDA the procedure to install a transvaginal was supposed to be minimally-invasive. The US Drug Watchdog now says, "The FDA is now saying transvaginal mesh failures is causing complications in patients such as erosion and infection. Women who experience transvaginal mesh failure may need to have numerous corrective surgeries, IV therapy, blood transfusions and drainage of hematomas or abscesses." The US Drug Watchdog is offering to help all US women, who are now victim's of the transvaginal mesh disaster get to the best possible attorneys, and the group is promising the attorneys will all be women. For more information victims of the Transvaginal Mesh Disaster are urged to contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog is indicating symptoms of a vaginal mesh implants may include:

• Pain during sexual intercourse caused by erosion.
• Mesh erosion through the vagina (the mesh is actually protruding out of the vaginal wall)
• Bleeding
• Vaginal Infection
• Urinary problems
• Organ perforation

The US Drug Watchdog says, "One of the biggest problems we have with respect to our failed medical device or recalled drug initiative work is the average US consumer never hears about a drug recall or failures involving medical devices like the Transvaginal Mesh Disaster. If you have a friend, or loved one who is a recipient of a Transvaginal Mesh that has already failed or is showing symptoms of a failure, please have them call us at 866-714-6466. We want to make certain these Transvaginal Mesh Disaster victims get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal, and we will do our absolute best to make certain all of the attorneys are women." http://USDrugWatchdog.Com

.

US Drug Watchdog Now Offers to Help All Recipients of a DePuy ASR Or DePuy Pinnacle Hip Implant Get To the Best Possible Attorneys-Out Of Fear Time Will Run Out For Them

Thursday, June 14, 2012

The US Drug Watchdog is now offering to assist all recipients of the recalled DePuy ASR metal on metal hip implant, along with DePuy's Pinnacle metal on metal hip implant get to the best possible attorneys because compensation is going to be vital due to a possibility these metal-on-metal hip implants will fail and need to be replaced now, or in the near future. In August of 2010 the DePuy ASR metal-on-metal hip implant was recalled, and there is now a national class action involving the DePuy Pinnacle metal-on-metal hip implant. The US Drug Watchdog says, "There are about 40,000 DePuy ASR recipients out there, and only about 3400 have been identified by the federal court handling that case, and of the 130,000+ DePuy Pinnacle metal-on-metal hip implant recipients out there only about 1000 have been identified by the federal court handling that case. Even if the hip implant has not yet failed, we will recommend the best possible law firms, in order to ensure these DePuy hip implant recipients do not get left at the curb holding the bag. If you have a DePuy ASR, or DePuy Pinnacle metal-on-metal hip implant, please call us at 866-714-6466, even if the device has not yet failed." http://USDrugWatchdog.Com

(PRWEB) June 14, 2012

The US Drug Watchdog is doing everything possible to assist victims of metal-on-metal hip implant failures in the US, including the DePuy ASR, and the DePuy Pinnacle metal, on metal hip implant devices. The US Drug Watchdog says, "Because we fear failures for the recalled DePuy ASR metal on metal hip implant, or the DePuy Pinnacle metal on metal hip implant that is now the subject of a national class action, we think it is vital to get every DePuy ASR and DePuy Pinnacle metal-on-metal hip implant recipient identified now, and we think it is imperative we get to these hip implant recipients to the best possible national caliber personal injury trial attorneys, in order to ensure these people are compensated for what they have already gone through, or could go through in the future. DePuy ASR or DePuy Pinnacle hip implant recipients can call us anytime at 866-714-6466." http://USDrugWatchdog.Com

Important Note From The US Drug Watchdog: "We have just learned there may be a August 2012 deadline to get all recalled DePuy ASR hip implant recipients identified, and we do not care if the hip implant has failed yet, or not."

The US Drug Watchdog indicates symptoms of a failure with the Recalled DePuy ASR, Or The DePuy Pinnacle Hip Implant Include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility
• Elevated levels of cobalt in the recipients blood.

The US Drug Watchdog is the premier medical device and pharmaceutical watchdog in the United States. The group says, "We want to make certain all DePuy Pinnacle hip implant recipients and all recalled DePuy ASR metal-on-metal hip implant recipients get to the best possible national caliber personal injury law firms or attorneys that have the best record in achieving superior results for their clients. In the instance of the DePuy Pinnacle metal-on-metal hip implant we could be talking about 100,000+ victims, and in the instance of the DePuy ASR we could be talking about 30,000+ victims, and we want to ensure every possible victim is identified, and compensated." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

DePuy Pinnacle Case Number U.S. District Court for the Northern District of Texas MDL. 2244

DePuy ASR Case Number Ohio Southern Federal District Court Case Number MDL No. 2197

US Drug Watchdog Launches An Aggressive National Initiative On The Transvaginal Mesh Disaster For Women And Offers The Names and Contacts Of The Best Women Attorneys

Tuesday, June 12, 2012

The US Drug Watchdog is launching an aggressive initiative designed to help women recipients of a transvaginal mesh, who are now severely damaged by this type of product. Transvaginal mesh was designed for women, who were suffering from pelvic organ prolapse and stress urinary incontinence. According to the US FDA the procedure to install a transvaginal was supposed to be minimally-invasive. The US Drug Watchdog now says, "The Transvaginal Mesh Disaster is the worst mess we have ever seen for women. The FDA is now saying transvaginal mesh failures is causing complications in patients such as erosion and infection. Patients who experience transvaginal mesh failure have needed corrective surgery, IV therapy, blood transfusions and drainage of hematomas or abscesses." The US Drug Watchdog is offering to help any victim of the transvaginal mesh disaster get to the best possible attorneys, and the group is promising the attorneys will all be women. For more information victims of the Transvaginal Mesh Disaster are urged to contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) June 12, 2012

The US Drug Watchdog says, "We may have thousands, or even tens of thousands of women in the United States, who are in unspeakable pain, or they have been damaged beyond comprehension, because they got sold a bill of goods, on what we are calling the Transvaginal Mesh Disaster." Transvaginal mesh failure occurs when the mesh fails to bind to the pelvic tissues. As a consequence of this, the body rejects the mesh that has been sewn into it. As a result, the transvagina mesh may start to poke its way through the vaginal wall and protrude out of the vaginal tissue. This complication is more commonly referred to as "erosion." Erosion may result in extreme pain, infection, bleeding or vaginal discharge. The US Drug Watchdog has begun a very aggressive initiative designed to assist women in the United States, in what they are referring to as the Transvaginal Mesh Disaster. The group is urging any woman, who has had the transvaginal mesh surgical procedure done, and now has developed severe complications to call them anytime at 866-714-6466. As part of its initiative the US Drug Watchdog is offering to send all US women, who are victims of this Transvaginal Mesh Disaster to national caliber attorneys-who are all women. http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our failed medical device or recalled drug initiative work is the average US consumer never hears about a drug recall or failures involving medical devices like the Transvaginal Mesh Disaster. If you have a friend, or loved one who is a recipient of a Transvaginal Mesh that has already failed or is showing symptoms of a failure, please have them call us at 866-714-6466. We want to make certain these Transvaginal Mesh Disaster victims get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal, and we will do our absolute best to make certain all of the attorneys are women." http://USDrugWatchdog.Com

U.S. District Court for the Southern District of West Virginia Multidistrict litigation (MDL) consolidates all similar cases into one courtroom and will include the Defendants:
C.R. Bard, Inc., (MDL No. 2187);
American Medical Systems Inc., MDL No. 2325);
Boston Scientific Corp., (MDL No. 2326); and Ethicon, Inc. (MDL No. 2327)

US Drug Watchdog Calls Its 'Osteoporosis Drug Fosamax & Women Who Have Had A Unexplainable Femur Fracture' One Of Its Most Important Initiatives Ever

Monday, June 11, 2012

The US Drug Watchdog says, "The osteoporosis drug called Fosamax, and out of the blue femur breaks is one of the most complicated issues we have ever encountered. For one, we are hearing from women, who were using Fosamax for five years or more, their femur broke, and typically they had to have at least one surgery to repair the femur. Often, if not in most cases these surgeries involve using a metal rod to reinforce the femur. Our greatest fear is most women, who have had this happen will never hear about the possible correlation between the osteoporosis drug called Fosamax, and their broken femur. We are urging family members of women, who have suffered a broken femur, to ask if they were also using Fosamax." On February 3rd 2011, The Journal of the American Medical Association (JAMA) came out with a Canadian medical study that points to a higher risk of a certain type of thighbone fracture in women who take bisphosphonates such as Fosamax for long periods. The US Drug Watchdog wants to hear from any woman, who was using the osteoporosis drug called Fosamax for five years, or more, and then suffered an unexplained femur break, also known as a thighbone break. For more information please contact the US Drug Watchdog at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) June 11, 2012

The US Drug Watchdog says, "It sounds counterintuitive, that a drug supposedly devised to fight osteoporosis could also be associated with women, who suffered an out of the blue broken femur bone. However, when it comes to the osteoporosis called Fosamax, that is exactly what we are saying. We are also saying we need family members, or loved ones of women, who suffered an out of the blue femur break to ask if the woman was also using the osteoporosis drug called Fosamax." The US Drug Watchdog is trying to identify every woman in the United States, who has been using, any type of osteoporosis drug, or the osteoporosis drug called Fosamax for at least five years, and then for some unexplained reason, they suffered a broken femur, thighbone, or what is called a atypical thigh fracture. According to the US FDA, "The femur fracture can happen suddenly and without warning, so this could be a particularly serious Fosamax side effect." The US Drug Watchdog is urging family members of women, who have suffered an out of the blue femur break to ask if they were using the osteoporosis drug called Fosamax. The group is urging any potential victim to call them anytime at 866-714-6466, or they can contact the group via its web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "We want to make certain all Fosamax users, or other osteoporosis type drug users, who suffered an unexplained broken femur, or thigh bone get to the best actual trial law firms or attorneys, that have a superior record in achieving significant results for their clients--period." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

MDL No. 2243-In re: Fosamax (Alendronate Sodium) Products Liability Litigation (No. II)

US Drug Watchdog Now Offers All Recipients Of The Recalled DePuy ASR Hip Implant The Names Of The Best Attorneys Because Of A Possible Looming Deadline

Tuesday, June 12, 2012

The US Drug Watchdog is offering to help all recipients of the recalled DePuy ASR get identified to the best possible attorneys, even if their metal-on-metal hip implant device has not yet failed. The group has heard of a possible looming deadline of August 2012-to have all recall DePuy ASR hip implant recipients identified. The group is concerned that once a settlement has been reached on the recalled DePuy ASR hip implant litigation, individuals who suffer a failure of the recalled hip implant may be up the creek, if they were not identified prior to the settlement. The US Drug Watchdog says," What has us horrified is only about 3400 individuals so far have been identified by the federal court in Ohio that is handling the litigation, and there are 40,000 DePuy ASR hip implant recipients. We intend to do everything possible to change this dynamic, with the goal being every DePuy ASR recipient gets identified by the court, and we can suggest the best possible attorneys to streamline the process. Before time runs out to get identified, if you, or a loved one has had a hip replacement involving the recalled DePuy ASR hip implant, please call us immediately at 866-714-6466." http://USDrugWatchdog.com

(PRWEB) June 12, 2012

The US Drug Watchdog says, "Because of the high failure rate associated with the now recalled DePuy ASR hip implant, we think it is absolutely vital to get every DePuy ASR hip implant recipient identified to the best possible attorneys, out of fear the device will fail prematurely, and or out of fear a possible deadline of August 2012 to have all recalled DePuy ASR hip implant recipients identified. Our biggest worry right now is of the 40,000 US citizens, who received a now recalled DePuy ASR hip implant, only about 3400 have been identified by the Ohio Federal Court, that is handling the litigation. Our number one priority is making certain every recalled DePuy ASR hip implant recipient has been identified by the best possible attorneys, so down the road, their rights are protected, should the hip implant fail prematurely." The US Drug Watchdog is encouraging all DePuy ASR recipients to call them, for an unequaled free service, that is focused on making certain no US consumer, that received a DePuy ASR hip implant, that has now been recalled, gets left holding the bag. For more information about the DePuy ASR hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

The US Drug Watchdog indicates symptoms of the recalled DePuy ASR hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility
• Elevated levels of cobalt in the recipients blood stream

The US Drug Watchdog is the premier advocate for medical device recipients, and pharmaceutical safety in the United States. The group says, "We think it is vital to get all DePuy ASR recipients identified now, because in our opinion it is a very important way to protect their future." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

DePuy ASR Case Number Ohio Southern Federal District Court Case Number MDL No. 2197

US Drug Watchdog Now Offers to Help All Recipients of a DePuy ASR or a DePuy Pinnacle Implant Failure Get to the Best Possible Attorneys-Why Get Left Holding The Bag?

Wednesday, May 23, 2012

The US Drug Watchdog is now offering to assist all recipients of the recalled DePuy ASR artificial hip, along with DePuy's Pinnacle artificial hip get the best possible attorneys because compensation is going to be vital due to the possibility these metal-on-metal hip implants could fail and need to be replaced. In August of 2010 the DePuy ASR metal-on-metal hip implant was recalled, and there is now a national class action involving the DePuy Pinnacle metal-on-metal hip implant. According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do." Fearing a failure now, or down the road we believe it is vital to get every DePuy ASR, and DePuy Pinnacle metal on metal hip implant recipient identified, and we will recommend the best possible law firms, in order to ensure these DePuy hip implant recipients do not get left at the curb holding the bag. If you have a DePuy ASR, or DePuy Pinnacle metal-on-metal hip implant, please call us at 866-714-6466, even if the device has not yet failed." http://USDrugWatchdog.Com

(PRWEB) May 23, 2012

The US Drug Watchdog says, "There are about 40,000 recalled DePuy ASR hip implant recipients out there, and only about 3500 have been identified by the federal court handling that case, and of the 130,000+ DePuy Pinnacle metal-on-metal hip implant recipients out there only about 1000 have been identified by the federal court handling that case. We need to get every recipient identified, just in case one of these metal on metal hip implants fails down the road, or if the device has already started to fail." As a background, the New York Times wrote an article about the US metal-on-metal hip disaster on December 27th 2011. In the article the Times said,"Some 500,000 patients have received an all-metal replacement hip, according to one estimate." The US Drug Watchdog says, "We think it is vital to get every recalled DePuy ASR and DePuy Pinnacle metal-on-metal hip implant recipient identified now, and we think it is imperative we get to these hip implant recipients to the best possible national caliber personal injury trial attorneys, to ensure these people are compensated for what they have already gone through, or could go through in the future. DePuy ASR or DePuy Pinnacle hip implant recipients can call us anytime at 866-714-6466." http://USDrugWatchdog.Com

The US Drug Watchdog indicates symptoms of a failure with the Recalled DePuy ASR, Or The DePuy Pinnacle Hip Implant Include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility
• High levels of cobalt in a recipients blood

The US Drug Watchdog is the premier medical device and pharmaceutical watchdog in the United States. The group says, "We want to make certain all DePuy Pinnacle hip implant recipients and all recalled DePuy ASR metal-on-metal hip implant recipients get to the best possible national caliber personal injury law firms or attorneys that have the best record in achieving superior results for their clients. In the instance of the DePuy Pinnacle metal-on-metal hip implant we could be talking about 100,000+ victims, and in the instance of the DePuy ASR we could be talking about 30,000+ victims, and we want to ensure every possible victim is identified, and compensated." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

US Drug Watchdog Now Offers to Assist All Recipients of a DePuy Pinnacle Or DePuy ASR Metal on Metal Hip Implant Get To the Best Possible Attorneys-Everyone One Counts

Monday, May 14, 2012

The US Drug Watchdog intends to become the premier advocate for all recipients of all metal-on-metal hip implants in the US, up to and including the DePuy ASR, and the DePuy Pinnacle metal, on metal hip implant devices. As a background, the New York Times wrote an article about the metal-on-metal hip disaster on December 27th 2011. In the article the Times said,"Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip, according to one estimate." The US Drug Watchdog says, "Because we fear failures for the recalled DePuy ASR metal on metal hip implant, or the DePuy Pinnacle metal on metal hip implant that is now the subject of a national class action, we think it is vital to get every DePuy ASR and DePuy Pinnacle metal-on-metal hip implant recipient identified now, and we think it is imperative we get to these hip implant recipients to the best possible national caliber personal injury trial attorneys, in order to ensure these people are compensated for what they have already gone through, or could go through in the future. DePuy ASR or DePuy Pinnacle hip implant recipients can call us anytime at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) May 14, 2012

The US Drug Watchdog is now offering to assist all recipients of the recalled DePuy ASR metal on metal hip implant, along with DePuy's Pinnacle metal on metal hip implant get to the best possible attorneys because compensation is going to be vital due to a possibility these metal-on-metal hip implants will fail and need to be replaced now, or in the near furure. In August of 2010 the DePuy ASR metal-on-metal hip implant was recalled, and there is now a national class action involving the DePuy Pinnacle metal-on-metal hip implant. According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do." The US Drug Watchdog says, "There are about 40,000 DePuy ASR recipients out there, and only about 3400 have been identified by the federal court handling that case, and of the 130,000+ DePuy Pinnacle metal-on-metal hip implant recipients out there only about 1000 have been identified by the federal court handling that case. Even if the hip implant has not yet failed, we will recommend the best possible law firms, in order to ensure these DePuy hip implant recipients do not get left at the curb holding the bag. If you have a DePuy ASR, or DePuy Pinnacle metal-on-metal hip implant, please call us at 866-714-6466, even if the device has not yet failed." http://USDrugWatchdog.Com

The US Drug Watchdog indicates symptoms of a failure with the Recalled DePuy ASR, Or The DePuy Pinnacle Hip Implant Include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility
• Elevated levels of cobalt in the recipients blood.

The US Drug Watchdog is the premier medical device and pharmaceutical watchdog in the United States. The group says, "We want to make certain all DePuy Pinnacle hip implant recipients and all recalled DePuy ASR metal-on-metal hip implant recipients get to the best possible national caliber personal injury law firms or attorneys that have the best record in achieving superior results for their clients. In the instance of the DePuy Pinnacle metal-on-metal hip implant we could be talking about 100,000+ victims, and in the instance of the DePuy ASR we could be talking about 30,000+ victims, For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

DePuy Pinnacle Case Number U.S. District Court for the Northern District of Texas MDL. 2244and we want to ensure every possible victim is identified, and compensated."

US Drug Watchdog Says Its Vital All DePuy Pinnacle Hip Implant Recipients Know The Symptoms Of A Failure And They Offer The Names Of The Best Attorneys If A Failure Occurs

Wednesday, April 25, 2012

The US Drug Watchdog says, "Because a hip implant failure, or hip replacement surgery is such a huge ordeal, we want to hear from every recipient of a metal-on-metal DePuy Pinnacle hip implant, out of fear their device has started to fail, or victims may not know the warning signs of a failure. Symptoms of a DePuy Pinnacle hip implant failure include pain, problems walking, swelling of the hip, or lack of flexibility." According to the New York Times, "Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip, according to one estimate." The US Drug Watchdog says, "We urgently need family members, or loved ones of a hip implant recipient, that was surgically installed between 2005, and 2010 to ask the family member, or friend, if it was a DePuy Pinnacle hip implant. We could easily have tens of thousands of US DePuy Pinnacle hip implant victims, living each day in pain, with a failed hip implant. Nothing is more important to us than trying to get all DePuy Pinnacle hip implant victims identified, to the best possible national caliber attorneys, and we will help with the process." For more information about the DePuy Pinnacle hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) April 25, 2012

The US Drug Watchdog says, "The symptoms of DePuy Pinnacle metal-on-metal hip implant failure include pain in the area of the hip implant, swelling in the area of the hip implant, lack of flexibility, or loss of mobility. Because DePuy Pinnacle hip implants were surgically installed on well over 100,000 US citizens, and because numerous studies are pointing to increased failure rates with all metal-on-metal hip implants, we are doing every thing possible to get every victim of a metal on metal hip implant failure identified, so we can make sure the get to the best possible attorneys. Because living with a failed hip implant, and or hip implant replacement surgery, also known as revision surgery are such traumatic events, we are very focused on victim compensation, when it comes to any type of metal-on-metal hip implant failure, including the DePuy Pinnacle." According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips, in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do. The wear of metal parts against each other is generating debris that is damaging tissue and, in some cases, crippling patients." The US Drug Watchdog says, "The DePuy Pinnacle Hip Implant is a metal-on-metal hip implant, and we think it is vital that every DePuy Pinnacle recipient understand the warning signs of a failure. At the same time we want to get every failed metal on metal hip implant victim identified. If you, or a loved one has had a hip replacement involving the metal-on-metal hip implant called the DePuy Pinnacle, the now recalled DePuy ASR hip implant, or any other metal on metal hip implant device that has failed please call us immediately at 866-714-6466." http://USDrugWatchdog.Com

The US Drug Watchdog's DePuy Pinnacle hip implant failure symptoms include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier medical device, and pharmaceutical watchdog, and advocate in the United States. The group says, "We want to make certain all metal-on-metal DePuy Pinnacle hip implant victims get to the actual trial law firms, or attorneys, that have the best record in achieving superior results for their clients, in these types of medical device lawsuits. Because compensation is vital, we think having the best, or most capable national caliber personal injury law firm is always the best choice." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

U.S. District Court for the Northern District of Texas MDL#2244

US Drug Watchdog Openly Mocks The US FDA For Doing Little To Nothing About The Metal On Metal Hip Implant Disaster & Offers To Help Victims Get To The Best Attorneys

Monday, April 23, 2012

The US Drug Watchdog is now openly mocking the US FDA for once again sitting on their hands, while up to half a million US citizens could now be stuck with a metal on metal hip implant device that might prematurely fail, or do even more damage because the metal debris could be giving these type of hip implant recipients blood poisoning. The United Kingdom is already on the verge of an out right ban of all metal on metal hip implants, and the US Drug Watchdog is convinced there are hundreds of thousands of US citizens, who are recipients of a metal-on-metal hip implant that has failed, or will fail prematurely. According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips, in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do. The wear of metal parts against each other is generating debris that is damaging tissue and, in some cases, crippling patients." The US Drug Watchdog wants to hear from any metal-on metal hip implant recipient if their hip implant has already failed, if the hip implant recipient is suffering the symptoms of a metal-on metal hip implant failure, or if the metal on metal hip implant recipient is concerned about a premature failure, in order to get them to the best attorneys. Metal on metal hip implant recipients are encouraged to contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) April 23, 2012

The US Drug Watchdog is openly mocking the US FDA for their do nothing approach to what the group considers to be a looming disaster for hundreds of thousands of US citizens, who are recipients of what is called a metal on metal hip implant device. While there has already been one notable metal on metal hip implant recall, the group is saying, "We are hearing from numerous other metal on metal hip implant recipients, and they do not have a recalled DePuy ASR. So we have completely redesigned our web site in order to ensure all recipients of a failed metal on metal hip implant know that they have not been forgotten, or ignored." The group expects there will be hundreds of thousands US metal-on-metal hip implant failure victims, and the US Drug Watchdog intends to create a seamless pathway where a US metal-on-metal hip implant recipient can get to the best possible personal injury attorneys; with the goal being compensation for what victims are going through, or what they might have to go through, should the hip implant prematurely fail. According to the New York Times, "Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip, according to one estimate." The US Drug Watchdog wants to hear from any US hip implant recipient, who received a metal on metal hip implant device after 2004, and whose metal-on-metal hip implant device has either already failed, or the recipient is experiencing symptoms of a hip implant failure that include swelling or pain in the region of the metal-on-metal hip implant and/or loss of mobility. For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

Symptoms of a metal-on-metal hip implant failure include pain in the area of the hip implant, loss of flexibility, swelling in the area of the metal-on metal hip implant or loss of mobility. Once again the US Drug Watchdog says, "Why have the US FDA constantly having to follow behind the Europeans by years, when it comes to medical device failures, like what we expect to see with the metal on metal hip disaster? We do not think most US citizens understand frequently FDA panelists resign from their positions at the US FDA, and go right back to work for a drug maker, or a medical device manufacturer. Are we the only group that has a problem with this?" http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our failed medical device or recalled drug initiative work is the average US consumer never hears about a drug recall or failures involving medical devices like metal-on-metal hip implants. If you have a friend, or loved one who is a recipient of a metal-on metal hip implant that has already failed or is showing symptoms of a failure, such as swelling, pain in the region of the hip, loss of flexibility or loss of mobility, please have them call us at 866-714-6466. We want to make certain these metal-on-metal hip implant victims get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal." http://USDrugWatchdog.Com

US Drug Watchdog Openly Mocks The US FDA For Doing Little To Nothing About The Metal On Metal Hip Implant Disaster & Offers To Help Victims Get To The Best Attorneys

Monday, April 23, 2012

The US Drug Watchdog is now openly mocking the US FDA for once again sitting on their hands, while up to half a million US citizens could now be stuck with a metal on metal hip implant device that might prematurely fail, or do even more damage because the metal debris could be giving these type of hip implant recipients blood poisoning. The United Kingdom is already on the verge of an out right ban of all metal on metal hip implants, and the US Drug Watchdog is convinced there are hundreds of thousands of US citizens, who are recipients of a metal-on-metal hip implant that has failed, or will fail prematurely. According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips, in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do. The wear of metal parts against each other is generating debris that is damaging tissue and, in some cases, crippling patients." The US Drug Watchdog wants to hear from any metal-on metal hip implant recipient if their hip implant has already failed, if the hip implant recipient is suffering the symptoms of a metal-on metal hip implant failure, or if the metal on metal hip implant recipient is concerned about a premature failure, in order to get them to the best attorneys. Metal on metal hip implant recipients are encouraged to contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) April 23, 2012

The US Drug Watchdog is openly mocking the US FDA for their do nothing approach to what the group considers to be a looming disaster for hundreds of thousands of US citizens, who are recipients of what is called a metal on metal hip implant device. While there has already been one notable metal on metal hip implant recall, the group is saying, "We are hearing from numerous other metal on metal hip implant recipients, and they do not have a recalled DePuy ASR. So we have completely redesigned our web site in order to ensure all recipients of a failed metal on metal hip implant know that they have not been forgotten, or ignored." The group expects there will be hundreds of thousands US metal-on-metal hip implant failure victims, and the US Drug Watchdog intends to create a seamless pathway where a US metal-on-metal hip implant recipient can get to the best possible personal injury attorneys; with the goal being compensation for what victims are going through, or what they might have to go through, should the hip implant prematurely fail. According to the New York Times, "Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip, according to one estimate." The US Drug Watchdog wants to hear from any US hip implant recipient, who received a metal on metal hip implant device after 2004, and whose metal-on-metal hip implant device has either already failed, or the recipient is experiencing symptoms of a hip implant failure that include swelling or pain in the region of the metal-on-metal hip implant and/or loss of mobility. For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

Symptoms of a metal-on-metal hip implant failure include pain in the area of the hip implant, loss of flexibility, swelling in the area of the metal-on metal hip implant or loss of mobility. Once again the US Drug Watchdog says, "Why have the US FDA constantly having to follow behind the Europeans by years, when it comes to medical device failures, like what we expect to see with the metal on metal hip disaster? We do not think most US citizens understand frequently FDA panelists resign from their positions at the US FDA, and go right back to work for a drug maker, or a medical device manufacturer. Are we the only group that has a problem with this?" http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our failed medical device or recalled drug initiative work is the average US consumer never hears about a drug recall or failures involving medical devices like metal-on-metal hip implants. If you have a friend, or loved one who is a recipient of a metal-on metal hip implant that has already failed or is showing symptoms of a failure, such as swelling, pain in the region of the hip, loss of flexibility or loss of mobility, please have them call us at 866-714-6466. We want to make certain these metal-on-metal hip implant victims get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal." http://USDrugWatchdog.Com

US Drug Watchdog Now Stresses Urgency In Identifying All Recipients of the DePuy Pinnacle & DePuy ASR Hip Implants And Offers The Contacts For Best Possible Attorneys

Monday, April 16, 2012

The US Drug Watchdog says, "We need to identify all US recipients of the recalled DePuy ASR hip implant and the DePuy Pinnacle hip implant, that is now subject to a national class action lawsuit, and do everything possible to get these people to the best possible national caliber attorneys, because compensation is going to matter, if one of these devices has a premature failure. These metal-on-metal artificial hips were surgically implanted on over one hundred and fifty thousand US citizens between 2005 and early 2010, and the courts so far have only identified about 4000 individuals? We need to get every recipient of the DePuy ASR, and the DePuy Pinnacle hip implant identified, and we will offer suggestions to the hip implant recipients as to the highest national caliber law firms, to advance their claim." Symptoms of a recalled DePuy ASR or DePuy Pinnacle hip implant failure include pain in the hip region, problems walking, swelling of the hip,or lack of flexibility in the area of the hip. The US Drug Watchdog says, "If you or a loved one has had a hip replacement involving the recalled DePuy ASR hip implant, or the DePuy Pinnacle metal-on-metal hip implant, that is also subject to national class action please call us immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) April 16, 2012

The US Drug Watchdog says, "Our DePuy Pinnacle hip implant initiative, and our initiative focused on the recalled DePuy ASR hip implants are our most vital medical device initiatives ever. We want to get every recipient of one of these metal-on-metal hip implant devices identified by the best possible national caliber attorneys, because compensation is going to be vital. Only about 3400 individuals have been identified, out of 40,000 recipients, for the recalled DePuy ASR hip implant device. Because of the high failure rate of the recalled DePuy ASR we need to get at least another 20,000 to 30,000 recipients identified, out of fear their device will prematurely fail in the future. In the instance of the DePuy Pinnacle metal-on-metal hip implant so far only about 1000 individual recipients have been identified by the federal court in Texas. The DePuy Pinnacle is now subject to a national class action, related to premature failures of this metal-on-metal hip implant device. Over 130,000 US citizens have received the DePuy Pinnacle metal-on-metal hip implant. Because the issue of metal-on-metal hip implant failures is so vital we believe at a minimum 70,000 US recipients of the DePuy Pinnacle should be identified by the court, if for no other reason, but as insurance." According to the New York Times on December 27th 2011, "Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip." For more information about the DePuy ASR hip implant recall, or the DePuy Pinnacle hip implant, that are both subject to national litigation recipients are urged to call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

Symptoms of the recalled Depuy ASR or a DePuy Pinnacle hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier advocate for medical device recipients, and pharmaceutical safety in the United States. The group says, "We want to make certain all recalled DePuy ASR, and or all DePuy Pinnacle metal on metal hip implant recipients get to the best possible national caliber trial law firms or attorneys that have the best record in achieving superior results for their clients. Because failure could still be in the future for any recipient, we think it is vital to identify all DePuy ASR, or DePuy Pinnacle recipients now, as an important way to protect their future." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

DePuy Pinnacle Case Number U.S. District Court for the Northern District of Texas MDL#2244

DePuy ASR Case Number Ohio Southern Federal District Court Case Number MDL No. 2197

US Drug Watchdog Now Offers to Help All Recipients of a DePuy ASR or a DePuy Pinnacle Implant, Get the Best Possible Attorneys Because Compensation Is Going to Be Vital

Monday, March 26, 2012

The US Drug Watchdog is now offering to assist all recipients of the recalled DePuy ASR artificial hip, along with DePuy's Pinnacle artificial hip get the best possible attorneys because compensation is going to be vital due to a very real possibility these metal-on-metal hip implants will fail and need to be replaced. In August of 2010 the DePuy ASR metal-on-metal hip implant was recalled, and there is now a national class action involving the DePuy Pinnacle metal-on-metal hip implant. According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do." The US Drug Watchdog says, "There are about 40,000 DePuy ASR recipients out there, and only about 3400 have been identified by the federal court handling that case, and of the 130,000+ DePuy Pinnacle metal-on-metal hip implant recipients out there only about 1000 have been identified by the federal court handling that case. From here on out we will be doing DePuy ASR and DePuy Pinnacle press releases everyday in order get as many recalled DePuy ASR and DePuy Pinnacle recipients identified, even if the hip implant has not yet failed, and we will recommend the best possible law firms, in order to insure these DePuy hip implant recipients do not get left at the curb holding the bag. If you have a DePuy ASR, or DePuy Pinnacle metal-on-metal hip implant, please call us at 866-714-6466, even if the device has not yet failed." http://USDrugWatchdog.Com

(PRWEB) March 26, 2012

The US Drug Watchdog is the premier advocate in the United States for defective medical devices and/or recalled pharmaceutical products, and because of the potential size of the US metal-on-metal defective hip disaster, the group intends to become the premier advocate for all recipients of all metal-on-metal hip implants in the US, up to and including the DePuy ASR, and the DePuy Pinnacle metal, on metal hip implant devices. As a background, the New York Times wrote an article about the metal-on-metal hip disaster on December 27th 2011. In the article the Times said,"Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip, according to one estimate." The US Drug Watchdog says, "Because we fear the recalled DePuy ASR, or the DePuy Pinnacle hip implants could possibly fail or have already failed, we think it is vital to get every DePuy ASR and DePuy Pinnacle metal-on-metal hip implant recipient identified now, and we think it is imperative we get to these hip implant recipients to the best possible national caliber personal injury trial attorneys, so we insure these people are compensated for what they have already gone through or could go through in the future. DePuy ASR or DePuy Pinnacle hip implant recipients can call us anytime at 866-714-6466." http://USDrugWatchdog.Com

The US Drug Watchdog indicates symptoms of a failure with the Recalled DePuy ASR, Or The DePuy Pinnacle Hip Implant Include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier medical device and pharmaceutical watchdog in the United States. The group says, "We want to make certain all DePuy Pinnacle hip implant recipients and all recalled DePuy ASR metal-on-metal hip implant recipients get to the best possible national caliber personal injury law firms or attorneys that have the best record in achieving superior results for their clients. In the instance of the DePuy Pinnacle metal-on-metal hip implant we could be talking about 100,000+ victims, and in the instance of the DePuy ASR we could be talking about 30,000+ victims, and we want to insure every possible victim is identified, and compensated." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

DePuy Pinnacle Case Number U.S. District Court for the Northern District of Texas MDL#2244

DePuy ASR Case Number Ohio Southern Federal District Court Case Number MDL No. 2197

US Drug Watchdog Rings Alarm Bells About Getting All Recalled DePuy ASR Hip Implant Recipients Identified To The Best Possible Attorneys Before Time Runs Out

Friday, March 23, 2012

The US Drug Watchdog is warning all recipients of the recalled DePuy ASR that it is vital they get identified by the best possible attorneys, even if their metal-on-metal hip implant device has not yet failed. The group is concerned that once a settlement has been reached on the recalled DePuy ASR hip implant litigation, individuals who suffer a failure of the recalled hip implant may be up the creek, if they were not identified prior to the settlement. The US Drug Watchdog says,"The DePuy ASR hip implants are failing, or have failed at an unacceptably high rate. As a result there was a recall on this hip implant device in August of 2010 by the US FDA. DePuy ASR hip implants were surgically implanted on about 40,000 US citizens between 2005 and mid 2010. What terrifies us is only about 3400 individuals have been identified by the federal court in Ohio that is handling the litigation. We intend to do everything possible to change this dynamic with the goal being every DePuy ASR recipient gets identified by the court, and we can suggest attorneys to streamline the process." According to the US FDA, symptoms of a recalled ASR DePuy hip implant failure include pain in the hip region, problems walking, swelling of the hip, or lack of flexibility in the area of the hip. The US Drug Watchdog is urging family members of hip implant recipients, who received a hip implant between 2005, and mid 2010, to ask if the hip implant was an ASR Depuy, and if they are having any problems. The US Drug Watchdog says, "If you, or a loved one has had a hip replacement involving the recalled DePuy ASR hip implant, please call us immediately at 866-714-6466." http://USDrugWatchdog.com

(PRWEB) March 23, 2012

The US Drug Watchdog says, "Our DePuy ASR recalled hip implant initiative is our most important recalled medical device initiative of ever. Unfortunately, because many individuals who received a ASR DePuy hip implant do not want to go through a painful hip replacement surgery, also called revision surgery, they do not complain. Because of this, we are strongly encouraging family members or loved ones of anyone receiving a hip implant between 2005 and early 2010 to ask if it was a DePuy ASR hip implant." They say, "even more worrisome to us is the fact that the DePuy ASR hip implant was sold as the right hip implant for younger adults who wanted to have an active or athletic lifestyle." The group says, "We could have tens of thousands of DePuy ASR hip implant victims in the US, and because of age, or not wanting to go through a hip replacement revision surgery again, they say nothing. Nothing is more important to us than trying to get them some meaningful help, that includes the best possible attorneys. At this point we do not care if the recalled DePuy ASR hip implant has not yet failed. We want to make certain all recipients are identified, in the event of a premature failure down the road." For more information about the DePuy ASR hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

The US Drug Watchdog indicates symptoms of the recalled DePuy ASR hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier advocate for medical device recipients, and pharmaceutical safety in the United States. The group says, "We think it is vital to get all DePuy ASR recipients identified now, because in our opinion it is a very important way to protect their future." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

DePuy ASR Case Number Ohio Southern Federal District Court Case Number MDL No. 2197

US Drug Watchdog Now Offers to Help All Recipients of the DePuy ASR & DePuy Pinnacle Hip Implant to Get to the Best Possible Attorneys Because Compensation is Vital

Monday, March 12, 2012

The US Drug Watchdog says, "Our current number one priority is to identify every recipient of the recalled DePuy ASR metal-on-metal and/or the DePuy Pinnacle hip implant, that are both named in national class action lawsuits, because we do not want these hip implant recipients missing out on what could be a huge settlement, and significant compensation. Our biggest fear is that--if the recalled DePuy ASR, or the DePuy Pinnacle recipients miss out on a settlement now, they could be up the creek down the road. For this reason, we are strongly encouraging family members, or loved ones of anyone receiving a hip implant between 2005 and early 2010 to ask if it was a DePuy ASR or DePuy Pinnacle hip implant." According to the New York Times on December 27th 2011, "Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip." The US Drug Watchdog says, "We firmly believe we have one hundred fifty thousand plus DePuy Pinnacle or DePuy ASR hip implant recipients in the US and, because of age or not wanting to go through a hip replacement revision surgery again, they say nothing. Nothing is more important to us than trying to get them some help, that includes the best possible attorneys." For more information about the DePuy ASR hip implant recall, or the DePuy Pinnacle hip implant, that are both subject to national litigation please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) March 12, 2012

The US Drug Watchdog says, "Because of the high failure rate associated with the DePuy ASR and DePuy Pinnacle hip implant, we believe it is vital we identify all US recipients of the recalled DePuy ASR hip implant and the DePuy Pinnacle hip implant that is now subject to a national class action lawsuit over the issue of failures. These metal-on-metal artificial hips were surgically implanted on over one hundred and fifty thousand US citizens between 2005 and early 2010, and the courts so far have only identified about 4000 individuals. We need to get every recipient identified, and we will offer suggestions to the hip implant recipients as to the highest national caliber law firms, to advance their claim." Symptoms of a recalled DePuy ASR or DePuy Pinnacle hip implant failure include pain in the hip region, problems walking, swelling of the hip,or lack of flexibility in the area of the hip. The US Drug Watchdog says, "If you or a loved one has had a hip replacement involving the recalled DePuy ASR hip implant, or the DePuy Pinnacle metal-on-metal hip implant, that is also subject to national class action please call us immediately at 866-714-6466." http://USDrugWatchdog.Com

Symptoms of the recalled Depuy ASR or a DePuy Pinnacle hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier advocate for medical device recipients, and pharmaceutical safety in the United States. The group says, "We want to make certain all DePuy ASR, or DePuy Pinnacle hip implant recipients get to the best possible national caliber trial law firms or attorneys that have the best record in achieving superior results for their clients. Because failure could still be in the future for any recipient, we think it is vital to get all DePuy ASR, or DePuy Pinnacle recipients now, as an important way to protect their future." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

US Drug Watchdog Urges All Recipients Of A DePuy Pinnacle Or ASR Hip Implant To Get Identified So They Can Get Legal Opinions About Compensation From The Best Attorneys

Tuesday, February 28, 2012

The US Drug Watchdog is saying, "Of the nearly 40,000+ recipients of the recalled DePuy ASR hip implant, only about 3300 hip implant failure victims have been identified-so far. In this instance we believe the number of individuals identified should be closer to 15,000 DePuy ASR hip implant recipients." The DePuy ASR was recalled in August of 2010. The US Drug Watchdog also says, "With respect to the DePuy Pinnacle hip implant over 100,000 were surgically implanted between 2005 & 2010 in the US, there is already a Federal Multi District Litigation over the DePuy Pinnacle hip implant, but our big worry here is only about nine hundred individuals have signed up so far." Both the DePuy ASR, and the DePuy Pinnacle metal-on-metal hip implants, have shown a high failure rate. According to the New York Times on December 27th 2011, "There is no data on the number of all-metal hips that have failed prematurely in this country because the outcomes of orthopedic procedures are not formally tracked by the government or private companies. But extrapolating from overseas data and the estimate of metal hip use here, tens of thousands of patients in the United States may have to undergo operations over the next decade to replace the implants." The US Drug Watchdog is saying, "Even if your DePuy ASR, or DePuy Pinnacle hip implant device has not failed-yet, we think it is vital we get you identified to the best possible attorneys, because we do not want metal-on-metal hip implant recipients left holding the bag financially ten years from now." For more information please call the US Drug Watchdog at 866-714-6466. http://USDrugWatchdog.Com

(PRWEB) February 28, 2012

The US Drug Watchdog says, "Even if your DePuy ASR hip implant has not yet failed, there is a good chance it will, so we believe you should positioned to be compensated in the event it will. With the issue of the DePuy Pinnacle metal-on-metal hip implant, we intend to grow the number of the Pinnacle hip implant failure victims, or potential victims to at last 30,000. Our Fear is once the lawsuits, or Multi District Litigations (MDL's) are over, DePuy ASR, or DePuy Pinnacle victims will have slim to none chances of meaningful recourse against the makers of these metal-on-metal hip implants." According to the US FDA, symptoms of a metal-on-metal hip implant failure include pain in the area of the metal-on-metal hip implant, loss of mobility, swelling in the area of the hip implant, loss of flexibility. According to the New York Times on December 27th 2011, " All-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip, according to one estimate. A new study found that no new artificial hip or knee introduced during a recent five-year period - implants that included some of the all-metal hips - were more durable than older devices, and 30 percent were worse." The US Drug Watchdog is urging all DePuy ASR, and all DePuy Pinnacle hip implant recipients to call them immediately so the group can get them identified to the best possible attorneys. DePuy ASR, or DePuy Pinnacle hip implant recipients can call the US Drug Watchdog anytime at 866-714-6466. http://USDrugWatchdog.Com

Symptoms of the recalled DePuy ASR hip implant, or DePuy Pinnacle hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility
• Possible colbalt blood poisoning

The US Drug Watchdog is the premier private pharmaceutical watchdog in the United States. The group says, "We want to make certain all DePuy ASR, or DePuy Pinnacle hip implant recipients get to the best possible national caliber trial law firms, or attorneys, that have the extraordinary track record in achieving superior results for their clients-period." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

US Drug Watchdog Says Its Vital We Now Identify All DePuy Pinnacle Hip Implant Recipients That Have A Hip Implant Failure & Its Critical Family Members Help

Wednesday, February 22, 2012

The US Drug Watchdog says, "There are over 100,000+ US citizens, who received a DePuy Pinnacle hip implant, and tragically many DePuy Pinnacle hip implants are failing, or have failed. As a result, a multi district litigation has begun, as a way to prosecute these claims. The DePuy Pinnacle hip implant is a metal-on-metal hip implant device. According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips, in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do. The wear of metal parts against each other is generating debris that is damaging tissue and, in some cases, crippling patients." Symptoms of a DePuy Pinnacle hip implant failure include pain in the hip region, problems walking, swelling of the hip, or lack of flexibility in the area of the hip. The US Drug Watchdog says, "If you, or a loved one has had a hip replacement involving the DePuy Pinnacle hip implant, please call us immediately at 866-714-6466." http://USDrugWatchdog.com

(PRWEB) February 22, 2012

The US Drug Watchdog says, "We could have tens, and tens of thousands of DePuy Pinnacle hip implant victims in the US, and because of age, or not wanting to go through a hip replacement revision surgery again, they say nothing. Nothing is more important to us than trying to get them some help." The US Drug Watchdog is strongly encouraging family members, or loved ones of anyone receiving a hip implant between 2005 and early 2010 to ask if it was a DePuy Pinnacle hip implant. According to the New York Times, "Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip, according to one estimate. A new study found that no new artificial hip or knee introduced during a recent five-year period - implants that included some of the all-metal hips - were more durable than older devices, and 30 percent were worse." The US Drug Watchdog says, "If you are a recipient, or a loved one is a recipient of a DePuy Pinnacle hip implant, that has already failed, or showing symptoms of a failure, we want to get you identified, and we want to make certain you get to the best possible national caliber personal injury law firms, to insure you receive the best possible compensation." For more information about the DePuy Pinnacle hip implant please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

The US Drug Watchdog indicates symptoms of a failure with the Depuy Pinnacle Hip Implant Include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

US Drug Watchdog Now Needs Family Members to Help Identify Recipients of the Recalled DePuy ASR Hip Implant Even if the Device Has Not Yet Failed

Friday, February 17, 2012

The US Drug Watchdog has just learned that of the approximately 33,000+ recipients of the DePuy ASR hip implant, only about 3300 have signed up for litigation focused on compensating them for a hip implant revision surgery, or the pain, and suffering, should such a surgery be required. Symptoms of a DePuy ASR hip implant failure include pain in the area of the hip implant, problems walking, swelling of the hip, or lack of flexibility. The group says, "It has already been very well documented that there is an extremely high failure rate for the ASR DePuy hip implants, and we need to get every victim identified as soon as possible, in order to try to get them some actual help, that could include significant compensation. We also believe that all recipients of the ASR hip implant should be identified by the court, in the event their hip implant fails in the future, and we have national caliber law firms in place to help recipients with this process." The DePuy hip implant device was used between 2005, and mid 2010. The US Drug Watchdog says, "If you, or a loved one has had a hip replacement involving the recalled ASR DePuy hip implant, be please call us immediately at 866-714-6466." http://USDrugWatchdog.Com.

(PRWEB) February 17, 2012

The US Drug Watchdog says, "We are strongly encouraging family members, or loved ones of anyone receiving a hip implant from 2005, until the summer of 2010 to ask if it was a ASR DePuy hip implant, out of fear the family member may not want to complain, or they have not heard of the recall." The group says, "At this moment there are only about 3300 DePuy ASR metal-on-metal recalled hip implant recipients signed up for the multi district litigation, and we fear the actual number should be well over 10,000. So we are doing everything possible to get the word out to all DePuy ASR recipients. This hip implant has been recalled, and we want to help you get signed up for the litigation." According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips, in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do. The wear of metal parts against each other is generating debris that is damaging tissue and, in some cases, crippling patients." The US Drug Watchdog is urging any recipient of a DePuy ASR hip implant to call them immediately at 866-714-6466. http://USDrugWatchdog.Com

Important Note: The US Drug Watchdog says, "We have learned the makers of the recalled ASR DePuy hip implant have been writing recipients of this hip implant, and offering to pay their co-pays for the replacement of this hip implant-what an insult." They say, "In reality, recipients of the recalled ASR DePuy hip implant might be owed hundreds of thousands of dollars, or more, and we find this manufacturers letter campaign to be nothing short of reprehensible. Offering to pay a co-pay-when the victim could be handicapped, or crippled for life?" http://USDrugWatchdog.Com

Symptoms of the recalled ASR Depuy hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier private pharmaceutical watchdog in the United States. The group says, "We want to make certain all ASR DePuy hip implant victims get to the actual trial law firms, or attorneys, that have the best record in achieving superior results for their clients-period." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com  Federal Case Number MDL No. 2197

US Drug Watchdog Now Wants To Hear From All US Metal-on-Metal Hip Implant Recipients Regardless Of Who Made It Because Of The High Failure Rates

Wednesday, February 8, 2012

The US Drug Watchdog is now beginning a very aggressive campaign designed to identify every US citizen, who is the recipient of any type of metal on metal hip implant device since 2004. The group says, "There appears to be an abnormally high failure rate for recipients of metal on metal hip implants starting from 2004 to the present. We are zeroing in on all metal-on-metal artificial hip implant manufacturers, and we want to hear from all recipients, who have already had revision surgery to have the failed device removed, or they are suffering from the symptoms of a metal-on metal hip implant failure that include swelling, lack of flexibility, pain in the hip region, or difficulty walking." According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips, in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do. The wear of metal parts against each other is generating debris that is damaging tissue and, in some cases, crippling patients." The US Drug Watchdog wants to hear from any metal-on metal hip implant recipient if their hip implant has already failed, or if the hip implant recipient is suffering the symptoms of a metal-on metal hip implant failure. Victims are encouraged to contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via the web site at http://USDrugWatchdog.Com

(PRWEB) February 08, 2012

The US Drug Watchdog is in the beginning stages of starting a national initiative focused on identifying all US metal-on-metal hip recipients, who have either had to have their metal-on metal implant replaced, or they are suffering symptoms of a metal-on-metal hip implant failure that include swelling, tenderness in the area of the hip implant, lack of flexibility, or lack of mobility. The US Drug Watchdog says, "We expect the metal-on metal hip implant initiative we are now beginning will be the largest defective medical device initiative we will ever be involved in. We expect numbers of victims to be in the 100,000's." According to the New York Times, "Until a recent sharp decline, all-metal implants accounted for nearly one-third of the estimated 250,000 hip replacements performed each year in the United States. Some 500,000 patients have received an all-metal replacement hip, according to one estimate. A new study found that no new artificial hip or knee introduced during a recent five-year period - implants that included some of the all-metal hips - were more durable than older devices, and 30 percent were worse." The US Drug Watchdog wants to hear from any US hip implant recipient, who received a metal, or metal hip implant device after 2003, and whose metal-on-metal hip implant device has either already failed, or the recipient is experiencing symptoms of a hip implant failure. For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our failed medical device, or recalled drug initiative work, is the average US consumer never hears about a drug recall, or failures involving medical devices like metal-on-metal hip implants. If you have a friend, or loved one, who is a recipient of a metal-on metal hip implant that has already failed, or is showing symptoms of a failure, such as swelling, pain in the region of the hip, loss of flexibility, or loss of mobility, please have them call us at 866-714-6466." http://USDrugWatchdog.Com

US Drug Watchdog Dramatically Intensifies Its Efforts To Insure Diabetics Who Used the Diabetes Drug Called Actos & Then Developed Bladder Cancer Get to the Best Lawyers

Wednesday, February 1, 2012

The US Drug Watchdog is warning diabetics, who used the diabetes drug called Actos, and then developed bladder cancer, to call them for the names, and contacts of the best possible national caliber personal injury attorneys to advance their claim. The US Drug Watchdog says, "We are tired of personal injury marketing law firms running ads on cable TV, that fail to mention the part about them selling an Actos case, to a real trial law firm, that will then advance the claim, so we are changing the rules. If you are a diabetic, who used the diabetes drug called Actos, and the developed bladder cancer, call us and we will give you the names, and specific contacts for extremely capable national caliber personal injury attorneys, and or law firms, that consistently get the best results-no middlemen." According to the AP, "The US FDA has also issued a warning about Actos, and bladder cancer. Both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." The US Drug Watchdog says, "We want to identify any user of the diabetes drug called Actos, if they have developed bladder cancer, and we think we will need the help of family members, and loved ones to get these victims identified." For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) February 01, 2012

The US Drug Watchdog has now refocused its initiative focused on diabetics, who used the diabetes drug called Actos, and then developed bladder cancer to insure all victims get directly to a national caliber personal injury law firm, that has a proven track record of consistently getting the best results for their clients, as opposed to a personal injury marketing law firm advertising on cable TV. The US Drug Watchdog says, "These diabetes drug cases, involving diabetics, who now have bladder cancer could be worth millions to the victims, and they should be. We do not see the value of a personal injury middleman marketing law firm doing ads on cable TV, and how they actually add value to the victim. An Actos diabetes drug user, who now has bladder cancer is not a commodity." According to the AP, "The FDA has issued a warning that Actos may be linked to an increased risk of bladder cancer. Meanwhile, both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." The US Drug Watchdog says, "We now fear bladder cancer, and diabetics using the diabetes drug called Actos is a much bigger problem than we ever dreamed possible, and we want to hear from any user of the diabetes medication called Actos, if they have developed bladder cancer, to insure they get the best possible legal representation. If after using Actos you, or a loved one developed bladder cancer please call our group immediately at 866-714-6466." http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. If you have a friend, or loved one, who was, or is using the diabetes drug called Actos, who has developed bladder cancer, please have them call us at 866-714-6466." http://USDrugWatchdog.Com

US Drug Watchdog Now Urges Diabetics Living with Bladder Cancer To Call Them Immediately If They Were Also Using the Diabetes Drug Called Actos

Tuesday, January 24, 2012

The US Drug Watchdog says, "It is hard for us to even comprehend the damages associated with diabetics, who were using the diabetes drug called Actos, and then developed bladder cancer, but we think the compensation owed to these victims is huge. We are urging loved ones, or family members to ask the question-were you using Actos before being diagnosed with bladder cancer? There may be a elevated incidence of bladder cancer for users of the diabetes drug called Actos, and we want to identify every US victim, in the hopes we can get them some meaningful help, and compensation." Actos is a member of a class of drugs known as thiazolidinediones, which have been linked to bladder cancer. Actos side effects include increased risk of congestive heart failure, and an increased risk for bladder cancer. According to the AP, "The US FDA has also issued a warning about Actos, and bladder cancer. Both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." The US Drug Watchdog says, "We want to identify any user of the diabetes drug called Actos, if they have developed bladder cancer, and we think we will need the help of family members, and loved ones to get these victims identified." For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) January 24, 2012

The US Drug Watchdog is now saying, "We completely underestimated the number of diabetics, who were using the diabetes drug called Actos, and then developed bladder cancer. We are now urging family members, or loved ones of diabetics, who have been diagnosed with bladder cancer, to ask if they were using the diabetes drug called Actos. Unfortunately, the use of Actos for diabetes, and an elevated chance of bladder cancer could to be related." According to the AP, "The FDA has issued a warning that Actos may be linked to an increased risk of bladder cancer. Meanwhile, both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." The US Drug Watchdog says, " We now fear bladder cancer, and diabetics using the diabetes drug called Actos is a much bigger problem than we ever dreamed possible, and we want to hear from any user of the diabetes medication called Actos, if they have developed bladder cancer, to insure they get the best possible legal representation. If after using Actos you, or a loved one developed bladder cancer please call our group immediately at 866-714-6466." http://USDrugWatchdog.Com

The US Drug Watchdog is the premier private pharmaceutical watchdog in the United States. The group says, "Tragically the Internet is loaded with misleading ads about Actos use, and bladder cancer compensation, lawsuits, or class actions. Unfortunately, most of the attorneys or law firms advertising for help with the diabetes drug called Actos, and bladder cancer are middlemen marketing law firms--not the actual trial law firms that will prosecute these cases." They say, "We want to make certain all Actos bladder cancer victims get to the actual trial law firms or attorneys that have the best record in achieving superior results for their clients--period--no middleman marketing law firms, or attorneys." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

Case number 11cv2406 BEN BGS in the Federal District Court San Diego, CA.

US Drug Watchdog Calls Its Osteoporosis Drug Fosamax Initiative & Women Who Have Had A Unexplainable Femur Fracture One Of Its Most Important Ever

Thursday, January 19, 2012

The US Drug Watchdog says, "It sounds counterintuitive, that a drug supposedly devised to fight osteoporosis could also be associated with women, who suffered an out of the blue broken femur bone. However, when it comes to the osteoporosis called Fosamax, that is exactly what we are saying. We are also saying we need family members, or loved ones of women, who suffered an out of the blue femur break to ask if the woman was also using the osteoporosis drug called Fosamax." The US Drug Watchdog is trying to identify every woman in the United States, who has been using, any type of osteoporosis drug, or the osteoporosis drug called Fosamax for at least five years, and then for some unexplained reason, they suffered a broken femur, thighbone, or what is called a atypical thigh fracture. According to the US FDA, "The femur fracture can happen suddenly and without warning, so this could be a particularly serious Fosamax side effect." The US Drug Watchdog is urging family members of women, who have suffered an out of the blue femur break to ask if they were using the osteoporosis drug called Fosamax. The group is urging any potential victim to call them anytime at 866-714-6466, or they can contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) January 19, 2012

The US Drug Watchdog says, "The osteoporosis drug called Fosamax, and out of the blue femur breaks is one of the most complicated issues we have ever encountered. For one, we are hearing from women, who were using Fosamax for five years or more, their femur broke, and typically they had to have at least one surgery to repair the femur. Often, if not in most cases these surgeries involve using a metal rod to reinforce the femur. Our greatest fear is most women, who have had this happen will never hear about the possible correlation between the osteoporosis drug called Fosamax, and their broken femur. We are urging family members of women, who have suffered a broken femur, to ask if they were also using Fosamax. One of the biggest problems, and challenges we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use." According to the FDA, "Typically these fractures occurred after using any type of osteoporosis drug, or Fosamax for five years, or more." On February 3rd 2011, The Journal of the American Medical Association (JAMA) came out with a Canadian medical study that points to a higher risk of a certain type of thighbone fracture in women who take bisphosphonates such as Fosamax for long periods. The US Drug Watchdog wants to hear from any woman, who was using the osteoporosis drug called Fosamax for five years, or more, and then suffered an unexplained femur break, also known as a thighbone break. For more information please contact the US Drug Watchdog at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "We want to make certain all Fosamax users, or other osteoporosis type drug users, who suffered an unexplained broken femur, or thigh bone get to the best actual trial law firms or attorneys, that have a superior record in achieving significant results for their clients--period." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

US Drug Watchdog Now Shifts Their Focus To Compensation & The Best Attorneys For Diabetics Who Used The Diabetes Drug Called Actos & Developed Bladder Cancer

Friday, January 20, 2012

The US Drug Watchdog says, "We are dramatically shifting our focus from a national campaign designed to identify diabetics, who used the diabetes drug called Actos, and then developed bladder cancer. We are now very focused on making certain Actos users, who developed bladder cancer have the very best trial attorneys, in order to make certain they get the best compensation. The victims, who developed bladder cancer have incredibly horrible stories, many lives have been ruined, and we fear many lives have been lost." There appears to be a correlation between US diabetics, bladder cancer, and the drug called Actos, and we want to identify every possible victim, in the hopes we can get them some meaningful help with respect to compensation, and helping the victim identify the most qualified national caliber lawyer to pursue the matter." Actos is a member of a class of drugs known as thiazolidinediones, which have been linked to bladder cancer. Actos side effects include increased risk of congestive heart failure, and an increased risk for bladder cancer. According to the AP, "The US FDA has also issued a warning about Actos, and bladder cancer. Both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." For more information Actos users, who now have bladder cancer, or their loved ones are encouraged to call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) January 20, 2012

The US Drug Watchdog is now calling its initiative focused on the diabetes drug called Actos, and diabetics who used this drug, and then developed bladder cancer, one of it's most vital initiatives ever, because of the damage done to these innocent victims. They say, "We want to identify every user of the diabetes drug called Actos, if they have developed bladder cancer, and we think we will need the help of family members, and loved ones to help get these victims identified. There may be a elevated incidence of bladder cancer for users of the diabetes drug called Actos, and we want to identify every US victim, in the hopes we can get them some meaningful help, and possibly significant financial compensation." http://USDrugWatchdog.Com

Actos is a member of a class of drugs known as thiazolidinediones, which have been linked to bladder cancer. Actos side effects include increased risk of congestive heart failure, and an increased risk for bladder cancer. According to the AP, "The US FDA has also issued a warning about Actos, and bladder cancer. Both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." For more information diabetics, who used the diabetes drug called Actos, who now have bladder cancer, or their loved ones are urged to call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. If you have a friend, or loved one, who was, or is using the diabetes drug called Actos, who has developed bladder cancer, please have them call us at 866-714-6466." http://USDrugWatchdog.Com

US Drug Watchdog Now Says It's Urgent We Get Family Members of Recipients Of The Recalled ASR DePuy Hip Implant To Help Us Identify Their Loved One

Tuesday, January 17, 2012

The US Drug Watchdog is strongly encouraging every recipient, or family member of a ASR DePuy hip implant to call the group immediately, if they are suffering pain, problems walking, swelling of the hip, or lack of flexibility The group says, "It has already been very well documented that there is an extremely high failure rate for the ASR DePuy hip implants, and we need to get every victim identified as soon as possible, in order to try to get them some actual help, that could include significant compensation." The DePuy hip implant device was used between 2005, and mid 2010. The US Drug Watchdog says, "If you, or a loved one has had a hip replacement involving the recalled ASR DePuy hip implant, be please call us immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) January 17, 2012

The US Drug Watchdog says, "We are strongly encouraging family members, or loved ones of anyone receiving a hip implant from 2005, until the summer of 2010 to ask if it was a ASR DePuy hip implant, out of fear the family member may not want to complain." The group says, "We could have tens of thousands of ASR DePuy hip implant victims in the US, and because of age, or not wanting to go through a hip replacement revision surgery again, they say nothing. Nothing is more important to us than trying to get them some help." For more information about the DePuy hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

Important Note:The US Drug Watchdog says, "We have learned the makers of the recalled ASR DePuy hip implant have been writing recipients of this hip implant, and offering to pay their co-pays for the replacement of this hip implant-what an insult." They say, "In reality, recipients of the recalled ASR DePuy hip implant might be owed hundreds of thousands of dollars, or more, and we find this manufacturers letter campaign to be nothing short of reprehensible. Offering to pay a co-pay-when the victim could be handicapped, or crippled for life?" http://USDrugWatchdog.Com

Symptoms of the recalled ASR Depuy hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier private pharmaceutical watchdog in the United States. The group says, "Tragically the Internet is loaded with misleading ads about ASR DePuy hip implant compensation, lawsuits, or class actions; unfortunately most of the attorneys, or law firms advertising for help with the ASR DePuy hip implant failures are middlemen marketing law firms-not the actual trial law firms that will prosecute these cases." They say, "We want to make certain all ASR DePuy hip implant victims get to the actual trial law firms, or attorneys, that have the best record in achieving superior results for their clients-period-no middleman marketing law firms, or attorneys." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

Federal Case Number MDL No. 2197

US Drug Watchdog Now Urges Diabetics Who Used The Diabetes Drug Actos And Now Have Bladder Cancer To Get Identified For Possible Legal Help & Compensation

Monday, January 9, 2012

The US Drug Watchdog is now saying, "We completely underestimated the number of diabetics, who were using the diabetes drug called Actos, and then developed bladder cancer. We are now urging family members, or loved ones of diabetics, who have been diagnosed with bladder cancer, to ask if they were using the diabetes drug called Actos. Unfortunately, the use of Actos for diabetes, and an elevated chance of bladder cancer could to be related." According to the AP, "The FDA has issued a warning that Actos may be linked to an increased risk of bladder cancer. Meanwhile, both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." The US Drug Watchdog says, " We now fear bladder cancer, and diabetics using the diabetes drug called Actos is a much bigger problem than we ever dreamed possible, and we want to hear from any user of the diabetes medication called Actos, if they have developed bladder cancer, to insure they get the best possible legal representation. If after using Actos you, or a loved one developed bladder cancer please call our group immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) January 09, 2012

The US Drug Watchdog says, "Few people would ever consider the possibility of a drug being used for diabetes, could also be related to elevated cases of bladder cancer. It is for this reason we need the help of loved ones, or family members of diabetics, who now have bladder cancer, to ask if the diabetic was, or is using the diabetes drug called Actos. There appears to be a correlation between US diabetics, bladder cancer, and the drug called Actos, and we want to identify every possible victim, in the hopes we can get them some meaningful help." Actos is a member of a class of drugs known as thiazolidinediones, which have been linked to bladder cancer. Actos side effects include increased risk of congestive heart failure, and an increased risk for bladder cancer. According to the AP, "The US FDA has also issued a warning about Actos, and bladder cancer. Both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." For more information Actos users, who now have bladder cancer, or their loved ones are encouraged to call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. If you have a friend, or loved one, who was, or is using the diabetes drug called Actos, who has developed bladder cancer, please have them call us at 866-714-6466." http://USDrugWatchdog.Com

The US Drug Watchdog is the premier private pharmaceutical watchdog in the United States. The group says, "Tragically the Internet is loaded with misleading ads about Actos use, and bladder cancer compensation, lawsuits, or class actions. Unfortunately, most of the attorneys or law firms advertising for help with the diabetes drug called Actos, and bladder cancer are middlemen marketing law firms--not the actual trial law firms that will prosecute these cases." They say, "We want to make certain all Actos bladder cancer victims get to the actual trial law firms or attorneys that have the best record in achieving superior results for their clients--period--no middleman marketing law firms, or attorneys." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

Case number 11cv2406 BEN BGS in the Federal District Court San Diego, CA.

US Drug Watchdog Now Calls Its Initiative for Diabetics Who Used the Diabetes Drug Actos and Then Developed Bladder Cancer Its Most Important Initiative for 2012
 

Thursday, January 5, 2012

The US Drug Watchdog says, "The US Drug Watchdog says, "Few people would ever consider the possibility of a drug being used for diabetes, could also be related to elevated cases of bladder cancer. It is for this reason we need the help of loved ones, or family members of diabetics, who now have bladder cancer, to ask if the diabetic was, or is using the diabetes drug called Actos. There appears to be a correlation between US diabetics, bladder cancer, and the diabetes drug called Actos, and we want to identify every possible victim in the hopes we can get them the best available help. We are calling our Actos Initiative for diabetics, who used the diabetes drug called Actos, and then developed bladder cancer, one of our most important pharmaceutical initiatives in 2012. According to the AP, "The FDA has issued a warning that Actos may be linked to an increased risk of bladder cancer. Meanwhile, both Germany and France have suspended sales of Actos. The Actos suspension became effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." ." They say, "We want to hear from any user of the diabetes medication called Actos, if they have developed bladder cancer. If after using Actos you, or a loved one developed bladder cancer please call our group immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) January 05, 2012

The US Drug Watchdog is now calling its initiative focused on the diabetes drug called Actos, and diabetics who used this drug, and then developed bladder cancer, one of its important initiatives ever. They say, "We want to identify every user of the diabetes drug called Actos, if they have developed bladder cancer, and we think we will need the help of family members, and loved ones to help get these victims identified. There may be a elevated incidence of bladder cancer for users of the diabetes drug called Actos, and we want to identify every US victim, in the hopes we can get them some meaningful help." http://USDrugWatchdog.Com

Actos is a member of a class of drugs known as thiazolidinediones, which have been linked to bladder cancer. Actos side effects include increased risk of congestive heart failure, and an increased risk for bladder cancer. According to the AP, "The US FDA has also issued a warning about Actos, and bladder cancer. Both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." For more information diabetics, who used the diabetes drug called Actos, who now have bladder cancer, or their loved ones are urged to call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. If you have a friend, or loved one, who was, or is using the diabetes drug called Actos, who has developed bladder cancer, please have them call us at 866-714-6466." http://USDrugWatchdog.Com

Case number 11cv2406 BEN BGS in the Federal District Court San Diego, CA.

US Drug Watchdog Says It's Vital We Identify All ASR DePuy Hip Implant Recipients & Its Critical Family Members Help Because Many DePuy ASR Recipients Won't Complain

The US Drug Watchdog says, "There are over 30,000 US citizens, who received a ASR DePuy hip implant, and tragically ASR DePuy hip implants are failing, or have failed at an unacceptably high rate. As a result there was a recall on this hip implant device in August of 2010 by the US FDA. DePuy ASR hip implants were surgically implanted on tens of thousands of US citizens between 2005 and early 2010." According to the US FDA, symptoms of a recalled ASR DePuy hip implant failure include pain in the hip region, problems walking, swelling of the hip, or lack of flexibility in the area of the hip. The US Drug Watchdog says, "Many US citizens, who received an ASR DePuy hip implant have been sent a letter by the device maker offering to pay their insurance co-pay? We say, if you received a recalled ASR DePuy hip implant, you are probably owed much more than a insurance co-pay, and we will try to help you find the best possible law firm to help you." The group is urging family members of hip implant recipients, who received a hip implant between 2005, and mid 2010, to ask if the hip implant was an ASR Depuy, and if they are having any problems. The US Drug Watchdog says, "If you, or a loved one has had a hip replacement involving the recalled ASR DePuy hip implant, please call us immediately at 866-714-6466." http://USDrugWatchdog.com

(PRWEB) January 06, 2012

The US Drug Watchdog says, "We could have tens of thousands of ASR DePuy hip implant victims in the US, and because of age, or not wanting to go through a hip replacement revision surgery again. Nothing is more important to us than trying to get them some help." The group fears because many individuals who received a ASR DePuy hip implant do not want to go through a painful hip replacement surgery, also called revision surgery, they do not complain. Because of this, the US Drug Watchdog is strongly encouraging family members or loved ones of anyone receiving a hip implant between 2005 and early 2010 to ask if it was a ASR DePuy hip implant." They say, "even more worrisome to us is the fact that the ASR DePuy hip implant was sold as the right hip implant for younger adults who wanted to have an active or athletic lifestyle." For more information about the DePuy hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

The US Drug Watchdog indicates symptoms of the recalled ASR DePuy hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier private pharmaceutical watchdog in the United States. The group says, "Tragically the Internet is loaded with misleading ads about ASR DePuy hip implant compensation, lawsuits, or class actions; unfortunately most of the attorneys or law firms advertising for help with the ASR DePuy hip implant failures are middlemen marketing law firms--not the actual trial law firms that will prosecute these cases." They say, "We want to make certain all ASR DePuy hip implant victims get to the actual trial law firms or attorneys that have the best record in achieving superior results for their clients--period--no middleman marketing law firms, or attorneys." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

US Drug Watchdog Now Urges All Women Who Have Had A Femur Or Thighbone Fracture To Call Them If The Injury Occurred While Using The Osteoporosis Drug Called Fosamax

Wednesday, January 4, 2012

The US Drug Watchdog says, "We intend to make femur breaks and the osteoporosis drug Fosamax one of our top initiatives in 2012. In the instance of Fosamax, we are talking about women, whose leg simply broke; they did not fall, they did not run into something, their femur, or upper thighbone simply broke. We need to identify every woman in the United States, who had been using, any type of osteoporosis drug, or the osteoporosis drug called Fosamax for at least five years, and then for some unexplained reason, they suffered a broken femur, thighbone or what is called a atypical thigh fracture." The group says, "One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. In the instance of the osteoporosis drugs, or specifically the osteoporosis drug called Fosamax, we are trying to identify women, who have used these types of drugs for five years, or more, and then for no apparent reason suffered a broken femur, or thigh bone." The type of leg breaks are also called atypical fractures associated with Fosamax. The fracture can happen suddenly and without warning, so this could be a particularly serious Fosamax side effect according to the US FDA. The US Drug Watchdog is urging women, or family members of women, who have used any osteoporosis drug, or the osteoporosis Fosamax for more than five years, and then suffered an unexplained broken femur, or thigh bone to contact them anytime at 866-714-6466, or they can contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) January 04, 2012

The US Drug Watchdog wants to hear from any woman, who suffered a out of the blue broken femur, or thighbone fracture, while they were using any osteoporosis drug, or the osteoporosis drug called Fosamax. According to the FDA, "Typically these fractures occurred after using any type of osteoporosis drug, or Fosamax for five years, or more." On February 3rd 2011, The Journal of the American Medical Association (JAMA) came out with a Canadian medical study that points to a higher risk of a certain type of thighbone fracture in women who take bisphosphonates such as Fosamax for long periods. The US Drug Watchdog wants to hear from any woman, who was using any osteoporosis drug, or the osteoporosis drug called Fosamax for five years, or more, and then suffered an unexplained femur break, also known as a thighbone break. For more information please contact the US Drug Watchdog at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says,"Most importantly we want to get the word out to women, who used Fosamax, or other osteoporosis drugs, who have suffered from an unexplainable broken femur, or broken leg. At the same time, we want to make certain all Fosamax users, or other osteoporosis type drug users, who suffered an unexplained broken femur, or thigh bone get to the actual trial law firms or attorneys, that have the best record in achieving superior results for their clients--period." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

MDL No. 2243-In re: Fosamax (Alendronate Sodium) Products Liability Litigation (No. II)

US Drug Watchdog Now Urges Loved Ones to Ask Their Women Family Members Who Have Suffered a Unexplained Femur Break if They Were Using the Osteoporosis Drug Fosamax

Wednesday, December 28, 2011

The US Drug Watchdog says, "In the instance of Fosamax, we are talking about women, whose leg simply broke. They did not fall, they did not run into something, their femur bone simply broke. We need to identify every woman in the United States, who had been using Fosamax for at least five years, and then for some unexplained reason they suffered a broken femur, or what is called an atypical thigh fracture." The US Drug Watchdog is urging family members, or loved ones of women, who have suffered an out of the blue femur break, or broken thigh bone, to ask the woman if she was using osteoporosis drug called Fosamax at the time of the break. According to the FDA on July 11th, 2011, "Typically these femur fractures among women occurred after using Fosamax for five years, or more." Women, who have used the osteoporosis drug Fosamax for more than five years, and then suffered an unexplained broken femur, or thigh bone are encouraged to contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) December 28, 2011

On February 3rd 2011, The Journal of the American Medical Association (JAMA) came out with a Canadian medical study that points to a higher risk of a certain type of femur, or thighbone fractures in women, who take bisphosphonates such as Fosamax for long periods of time. The US Drug Watchdog is saying, "One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. In the instance of the osteoporosis drug called Fosamax, we are trying to identify women, who have used this drug for five years, or more, and then for no apparent reason suffered a broken femur, or thigh bone, and we think we need loved ones, and or family members to help us identify these possible victims. These type of leg breaks are also called atypical fractures. These fracture can happen suddenly and without warning, so based on the JAMA study, this could be a particularly serious side effect of the osteoporosis drug called Fosamax." The US Drug Watchdog wants to hear from any woman, who was using the osteoporosis drug Fosamax for five years, or more, and then suffered an unexplained femur break, also known as a thighbone break. For more information please contact the US Drug Watchdog at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog is the premier private pharmaceutical watchdog, and advocacy group in the United States. The group says,"Most importantly we want to get the word out about Fosamax, and to long term users, who have suffered from an unexplainable broken femur, or broken leg. At the same time, we want to make certain all Fosamax users, who suffered an unexplained broken femur, or thigh bone get to the actual trial law firms or attorneys, that have the best record in achieving superior results for their clients-period." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

MDL No. 2243?"In re: Fosamax (Alendronate Sodium) Products Liability Litigation (No. II)

US Drug Watchdog Initiates New National Outreach Program Designed to Discover if Diabetics Now Living with Bladder Cancer Were Also Using the Diabetes Drug Called Actos

Monday, December 19, 2011

The US Drug Watchdog says, "No one would ever consider the possibility of a drug used for diabetes could also be related to elevated cases of bladder cancer. Unfortunately, the use of Actos for diabetes, and an elevated chance of bladder cancer could to be related. We need the help of loved ones, or family members of diabetics, who now have bladder cancer, to ask if the diabetic was using, or has also used the drug called Actos. There appears to be a correlation between US diabetics, bladder cancer, and the drug called Actos, and we want to identify every possible victim." According to the AP, "The FDA has issued a warning that Actos may be linked to an increased risk of bladder cancer. Meanwhile, both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." The US Drug Watchdog says, "We want to hear from any user of the diabetes medication called Actos, if they have developed bladder cancer. If after using Actos you, or a loved one developed bladder cancer please call our group immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) December 19, 2011

The US Drug Watchdog says, "We do not think the average bladder cancer victim, who was also a diabetic would ever consider a drug for diabetics could have been a contributing factor for bladder cancer, so we are urging loved ones, or family members to ask the question-were you using Actos before being diagnosed with bladder cancer? There may be a elevated incidence of bladder cancer for users of the diabetes drug called Actos, and we want to identify every US victim, in the hopes we can get them some meaningful help." Actos is a member of a class of drugs known as thiazolidinediones, which have been linked to bladder cancer. Actos side effects include increased risk of congestive heart failure, and an increased risk for bladder cancer. According to the AP, "The US FDA has also issued a warning about Actos, and bladder cancer. Both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." The US Drug Watchdog says, "We want to identify any user of the diabetes drug called Actos, if they have developed bladder cancer, and we think we will need the help of family members, and loved ones to get these victims identified." For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. If you have a friend, or loved one, who was, or is using the diabetes drug called Actos, who has developed bladder cancer, please have them call us at 866-714-6466." http://USDrugWatchdog.Com

Case number 11cv2406 BEN BGS in the Federal District Court San Diego, CA.

The US Drug Watchdog Urges Family Members or Loved Ones of Diabetics Who Now Have Bladder Cancer if They Were Using the Drug Called Actos

Monday, December 12, 2011

The US Drug Watchdog says, "We need the help of loved ones, or family members of diabetics, who now have bladder cancer, if they were, or have also used the drug called Actos. There appears to be a correlation between US diabetics, bladder cancer, and the drug called Actos, and we want to identify every possible victim." Both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication. The US Drug Watchdog says, "We want to hear from any user of the diabetes medication called Actos, if they have developed bladder cancer. If after using Actos you, or a loved one developed bladder cancer please call our group immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) December 12, 2011

The US Drug Watchdog says, "We are urging family members, or loved ones of US diabetics, who have developed bladder cancer, to ask if the bladder cancer victim was also using the drug called Actos. This is a very big deal, and we want to get every US diabetic, who was using Actos, and then developed bladder cancer identified. We do not think the average bladder cancer victim, who was also a diabetic would ever consider a drug for diabetics could have been a contributing factor for bladder cancer, so we are urging loved ones, or family members to ask the question. There may be a elevated incidence of bladder cancer for users of the diabetes drug called Actos, and we want to identify every US victim, in the hopes we can get them some meaningful help." Actos is a member of a class of drugs known as thiazolidinediones, which have been linked to bladder cancer. Actos side effects include increased risk of congestive heart failure, and an increased risk for bladder cancer. The US Drug Watchdog says, "We want to identify any user of the diabetes drug called Actos, if they have developed bladder cancer, and we think we will need the help of family members, and loved ones to get these victims identified." For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. If you have a friend, or loved one, who was, or is using the diabetes drug called Actos, who has developed bladder cancer, please have them call us at 866-714-6466." http://USDrugWatchdog.Com

Case number 11cv2406 BEN BGS in the Federal District Court San Diego, CA.

US Drug Watchdog Now Urges All Recipients Of The ASR DePuy Hip Implant To Get Identified Even If The Hip Implant Has Yet To Fail

PRWeb – 8 hrs ago

The US Drug Watchdog says, "We want to hear from every recipient of a ASR DePuy hip implant, out of fear their device has not yet failed, or it has started to fail, or victims may not know the warning signs of a failure. Symptoms include pain, problems walking, swelling of the hip, or lack of flexibility." There are close to 35,000 US citizens, who received a DePuy hip implant between 2005, and the first quarter of 2010, and the group wants to hear from every recipient, in order to see if the ASR DePuy hip implant has failed, or is in the process of failing. The group says, "It has already been well documented that there is an extremely high failure rate for the ASR DePuy hip implants. We have heard from ASR DePuy hip implant victims, and we now believe its vital to get every victim, or potential victim identified as soon as possible, in order to try to assist them in getting meaningful help." They say, "If you, or a loved one has had a hip replacement involving the recalled ASR DePuy hip implant, be please call us immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) November 28, 2011

The US Drug Watchdog says, "We are offering to assist every recipient of a ASR DePuy hip implant to determine if their hip implant has already failed, it is in the process of failing, or explain what we know about the potential for failures. We urgently need family members, or loved ones of a hip implant recipient, that was surgically installed between 2005, and early 2010 to ask the family member, or friend, if it was a DePuy hip implant, also known as a ASR DePuy hip implant." They say, "many US ASR DePuy hip implant victims are elderly, or senior citizens, and we are very worried the majority of victims will not complain, even if they are suffering pain, having problems walking, have swelling of the hip, or have lost flexibility. These hip implants were also sold to younger adults as the quote en quote athletic hip implant, for adults wanting an active lifestyle." They say, "According to numerous studies the ASR DePuy hip implant has a very high failure rate, and we think its vital, we do our best to identify all victims." The US Drug Watchdog fears there are 10,000's US ASR DePuy hip implant recipients living in horrible pain, or they are not aware of the recall. The group says, "We could easily have tens of thousands of US DePuy hip implant victims, living each day with a failed hip implant. Nothing is more important to us than trying to getting all ASR DePuy hip implant victims identified, and we will help with the process." For more information about the DePuy hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

The US Drug Watchdog's ASR DePuy hip implant failure symptoms include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier private pharmaceutical watchdog, and advocate in the United States. The group says, "Tragically the Internet is loaded with misleading advertisements about ASR DePuy hip implant compensation, lawsuits, or class actions; unfortunately most of the attorneys, or law firms advertising for help with the ASR DePuy hip implant failures are middlemen marketing law firms-not the actual trial law firms, that will prosecute these cases." They say, "We want to make certain all ASR Depuy hip implant victims gets to the actual trial law firms, or attorneys, that have the best record in achieving superior results for their clients." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

Federal Case Number MDL No. 2197

The US Drug Watchdog Initiates A National Investigation Of The Diabetes Drug Called Actos & Wants To Hear From Any User If They Developed Bladder Cancer

Monday, November 21, 2011

The US Drug Watchdog wants to hear from any user of the diabetes drug called Actos, who developed bladder cancer. According to the AP, "The FDA has issued a warning that Actos may be linked to an increased risk of bladder cancer. Meanwhile, both Germany and France have suspended sales of Actos. The Actos suspension is effective July 11, 2011. Actos (pioglitazone), along with another diabetes drug made by Takeda Pharmaceutical, Competact, came under fire in Europe after a study revealed an increased risk for bladder cancer among diabetes patients who were taking the medication." The US Drug Watchdog says, "We want to hear from any user of the diabetes medication called Actos, if they have developed bladder cancer. If after using Actos you developed bladder cancer please call our group immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) November 21, 2011

The US Drug Watchdog says, "Actos is a member of a class of drugs known as thiazolidinediones, which have been linked to bladder cancer. Actos side effects include increased risk of congestive heart failure, and an increased risk for bladder cancer." In August 2011, the first lawsuits were filed against Actos manufacturer Takeda Pharmaceuticals blaming the diabetes drug for instances of bladder cancer. Victims are suing for financial compensation for the cost of hospital bills and loss of income, as well as physical and emotional suffering. Legal experts predict that these are the first of many Actos lawsuits that will be filed.The US Drug Watchdog says, "We want to identify any user of the diabetes drug called Actos, if they have developed bladder cancer." For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says,"One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. If you have a friend, or loved one, who was, or is using the diabetes drug called Actos, who then developed bladder cancer, please have them call us at 866-714-6466." http://USDrugWatchdog.Com

Case number Federal District Court San Diego, CA 11cv2406 BEN BGS

US Drug Watchdog Targets Diet Pill Or Dietary Supplements Frequently Advertised On Cable TV And Consumers Who've Been Ripped Off For Hundreds Or Thousands Of Dollars

Sunday, November 13, 2011

The US Drug Watchdog is targeting makers of diet pills, or dietary supplements, that more often than not do not work, or these diet pills, or dietary supplements do not produce a dramatic weight loss,or health improvement as advertised on cable TV, or in a slick magazine advertisement. The group says, "Almost all of the weight loss pills, or dietary supplements advertised on cable TV, or in magazine advertisements have not been approved by the U.S. FDA, we don't think most work, it's a $20 billion dollar a year business in the United States, and frequently the only active ingredient is caffeine. We want to identify every victim, who feels like they were fleeced, after purchasing a too good to be true diet pill, or a dietary supplement." Victims of the weight loss pill, or the dietary supplement scam are encouraged to contact the US Drug Watchdog at 866-714-6466, or they can contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) November 13, 2011

The US Drug Watchdog is the premier watchdog in the United States for dangerous drugs, or ineffective medical products. The group is now zeroing in on the phoney diet pill, or dietary supplement, makers who frequently push their products on cable TV, or in slick magazine ads. The US Drug Watchdog wants to identify victims, who called an 800 toll free number to purchase a miracle diet pill, or the magical dietary supplement, after viewing a TV ad on cable TV, or after seeing a slick ad in a magazine, only to discover the diet pill, or dietary supplement did not work, or it made the consumer sick.

The US Drug Watchdog says, "We want to hear from anyone, who purchased a diet pill, or formula, and or a dietary supplement, being touted on a cable TV ad, or in a slick magazine ad, who feel like they got taken to the cleaners, because either the product did not work, or it actually made the consumer sick. Non FDA approved diet pills, and or dietary supplements are totally unregulated, and we think the makers of these diet pills, or dietary supplements are robbing innocent US consumers, with their ineffective products, and we want to hear from any victim." The US Drug Watchdog wants to hear from any consumer in the United States, who purchased a diet pill, or dietary supplement, that did not perform as advertised, or it actually made the consumer sick. For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "We believe our cable TV diet pill, or dietary supplement initiatives will turn out to be one of our most important initiatives ever. We know this is a multi billion dollar a year business, and we also know many of these diet pills, or dietary supplements either produce no positive impact for the consumer, or they actually put the user at risk. We intend to put a stop to this nonsense." http://USDrugWatchdog.Com

US Drug Watchdog Urges All Women Who Suffered Femur Or Thighbone Fractures To Call Them If The Injury Occurred While Using Any Osteoporosis Drug Or Fosamax

Tuesday, November 8, 2011

The US Drug Watchdog wants to hear from any woman, who suffered a out of the blue broken femur, or thighbone fracture, while they were using any osteoporosis drug, or the osteoporosis drug called Fosamax. According to the FDA, "Typically these fractures occurred after using any type of osteoporosis drug, or Fosamax for five years, or more." The US Drug Watchdog says, "In the instance of Fosamax, we are talking about women, whose leg simply broke. They did not fall, they did not run into something, their femur, or upper thighbone simply broke. We need to identify every woman in the United States, who had been using, any type of osteoporosis drug, or the osteoporosis drug called Fosamax for at least five years, and then for some unexplained reason, they suffered a broken femur, thighbone or what is called a atypical thigh fracture." Women, who have used any osteoporosis drug, or the osteoporosis Fosamax for more than five years, and then suffered an unexplained broken femur, or thigh bone are encouraged to contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) November 08, 2011

The US Drug Watchdog says,"One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. In the instance of the osteoporosis drugs, or specifically the osteoporosis drug called Fosamax, we are trying to identify women, who have used these types of drug for five years, or more, and then for no apparent reason suffered a broken femur, or thigh bone. These type of leg breaks are also called atypical fractures.The fracture can happen suddenly and without warning, so this could be a particularly serious Fosamax side effect." On February 3rd 2011, The Journal of the American Medical Association (JAMA) came out with a Canadian medical study that points to a higher risk of a certain type of thighbone fracture in women who take bisphosphonates such as Fosamax for long periods. The US Drug Watchdog wants to hear from any woman, who was using any osteoporosis drug, or the osteoporosis drug called Fosamax for five years, or more, and then suffered an unexplained femur break, also known as a thighbone break. For more information please contact the US Drug Watchdog at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog says,"Most importantly we want to get the word out to long term women, who used Fosamax, or other osteoporosis drugs, who have suffered from an unexplainable broken femur, or broken leg. At the same time, we want to make certain all Fosamax users, or other osteoporosis type drug users, who suffered an unexplained broken femur, or thigh bone get to the actual trial law firms or attorneys, that have the best record in achieving superior results for their clients--period." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

MDL No. 2243-In re: Fosamax (Alendronate Sodium) Products Liability Litigation (No. II)

US Drug Watchdog Launches a Vital Campaign for Consumers Who Have Been Fleeced by Ineffective Diet Pills, or Dietary Supplements Frequently Advertised on Cable TV

Monday, October 31, 2011

The US Drug Watchdog is launching a vital campaign aimed at identifying innocent consumers, who were led to believe they could see a dramatic weight loss, or improvement in their health, after buying a dietary supplement, or weight loss pill, that was featured on a cable TV ad, or in a magazine. The group says, "Almost all of the weight loss pills, or dietary supplements advertised on cable TV, or in magazine advertisements have not been approved by the U.S. FDA, we don't think most work, and it's a $20 billion dollar a year business in the United States. We want to identify any victim, who feels like they were fleeced, after purchasing a too good to be true diet pill, or a dietary supplement." Victims of the weight loss pill, or dietary supplement scam are encouraged to contact the US Drug Watchdog at 866-714-6466, or they can contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) October 31, 2011

The US Drug Watchdog is the premier watchdog in the United States for dangerous drugs, or ineffective medical products. The group is focused on identifying victims, who called an 800 toll free number to buy a miracle diet pill, or the magical dietary supplement, after viewing a TV ad on cable TV, or after seeing a slick ad in a magazine, only to discover the diet pill, or dietary supplement did not work, or it made the consumer sick. The US Drug Watchdog says, "We want to hear from anyone, who purchased a diet pill, or formula, and or a dietary supplement, being touted on a cable TV ad, or in a slick magazine ad, who feel like they got taken to the cleaners, because either the product did not work, or it actually made the consumer sick. Non FDA approved diet pills, and or dietary supplements are totally unregulated, and they are a $20 billion dollar a year industry in the United States." The US Drug Watchdog wants to hear from any consumer in the United States, who purchased a diet pill, or dietary supplement, that did not perform as advertised, or it actually made the consumer sick. For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "We believe our cable TV diet pill, or dietary supplement initiatives will turn out to be one of our most important initiatives ever. We know this is a multi billion dollar a year business, and we also know many of these diet pills, or dietary supplements either do nothing, or they actually put the user at risk. We intend to put a stop to this nonsense." http://USDrugWatchdog.Com

US Drug Watchdog Urges National Awareness of the FDA Recalled Colorado Cantaloupe Because of the Listeria Outbreak & Encourages Diagnosed Victims to Call Them

Sunday, October 2, 2011

The US Drug Watchdog is urging consumers in Arizona, Arkansas, Colorado, California, Florida, Illinois, Indiana, Kansas, Minnesota, Missouri, Montana, Nebraska, New Jersey, New Mexico, New York, North Dakota, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Utah, West Virginia, and Wyoming, to be on the lookout for severe flu like symptoms, if they ate cantaloupe purchased prior to September 14th 2011. States where the contaminated Colorado cantaloupes have cause fatalities include New Mexico, Colorado and Texas, Kansas, Maryland, Missouri, Nebraska, and Oklahoma. The US Drug Watchdog says, "The cause for our serious warning is the type of bacteria found in the recalled cantaloupe called Listeria. Listeria can grow even at low temperatures and can also can take three weeks or longer to make a person sick, so more cases will emerge in the coming weeks, or months. Currently 15 U.S. citizens have died from the recalled Colorado Cantaloupe, and we expect this number to grow. We are especially concerned about the elderly, pregnant women, and young children." The group says, "If you live in one of these states, and you, or family members ate cantaloupe in July, August, or September, and then became ill with flu like symptoms, or were hospitalized, we want to know about it." For more information consumer can contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group at http://USDrugWatchdog.Com

(PRWEB) October 02, 2011

The US Drug Watchdog is the premier advocate for consumers dealing with recalled drugs, or medical devices, and they are making a concerted effort to get the word out about the recalled Colorado cantaloupes to all residents, in at least 24 U.S. States. The recalled Colorado cantaloupe may contain a bacteria called Listeria. The illness associated with Listeria, is known as Listeriosis. Listeriosis is a rare and serious illness that mostly affects older adults, pregnant women, newborns and those with compromised immune systems. A person who comes down with it usually experiences fever, muscle aches, diarrhea and confusion. The infection almost always spreads to the gastrointestinal tract, and it can cause miscarriages and stillbirths in pregnant women, according to health officials. The US Drug Watchdog is urging all news media outlets in Arizona, Arkansas, Colorado, California, Florida, Illinois, Indiana, Kansas, Minnesota, Missouri, Montana, Nebraska, New Jersey, New Mexico, New York, North Dakota, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Utah, West Virginia, and Wyoming to tell their listeners, or remind their readers to be on the lookout for flu like symptoms, if they have eaten cantaloupe within the last 60 days or more. The group says, "Listeria has a relatively long shelf live, we are certain U.S. citizens were dying long before the US Food and Drug Administration became aware of the problem, and we need consumers, and healthcare professionals to be on alert. This is a huge mess, and we are long way from being out of the woods at this point." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

The US Drug Watchdog says, "If a family member, especially a senior citizen, or child died in August, or September from flu like symptoms, or a pregnant woman miscarried, and cantaloupe was a common denominator in the live style of these individuals, especially in the states we have listed, we want to know about it. Again, we need the news media in at least the states we have mentioned to remind their viewers, and readers about the Colorado cantaloupe recall, and the fact the severe risks are still out there, and will be for at least another two months." For more information potential victims, or family members of potential victims are welcome to call the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via their web site at http://USDrugWatchdog.Com

US Drug Watchdog Launches A Vital Investigation Involving Women Who Suffered Femur Or Thighbone fractures While Using The Osteoporosis Drug Fosamax

August 5, 2011

The US Drug Watchdog is launching a vital investigation involving the osteoporosis drug called Fosamax, and women who may have suffered out of the blue fractures to their femur, or thigh bone. According to the FDA, "typically these fractures occurred after using Fosamax for five years, or more." The US Drug Watchdog says, "In the instance of Fosamax, we are talking about women, whose leg simply broke. They did not fall, they did not run into something, their femur bone simply broke. We need to identify every woman in the United States, who had been using Fosamax for at least five years, and then for some unexplained reason, they suffered a broken femur, or what is called a atypical thigh fracture." Women, who have used the osteoporosis drug Fosamax for more than five years, and then suffered an unexplained broken femur, or thigh bone are encouraged to contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) August 04, 2011

The US Drug Watchdog says,”One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug’s use. In the instance of the osteoporosis drug called Fosamax, we are trying to identify women, who have used this drug for five years, or more, and then for no apparent reason suffered a broken femur, or thigh bone. These type of leg breaks are also called atypical fractures.The fracture can happen suddenly and without warning, so this could be a particularly serious Fosamax side effect.” On February 3rd 2011, The Journal of the American Medical Association (JAMA) came out with a Canadian medical study that points to a higher risk of a certain type of thighbone fracture in women who take bisphosphonates such as Fosamax for long periods. The US Drug Watchdog wants to hear from any woman, who was using the osteoporosis drug Fosamax for five years, or more, and then suffered an unexplained femur break, also known as a thighbone break. For more information please contact the US Drug Watchdog at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

The US Drug Watchdog is the premier private pharmaceutical watchdog, and advocacy group in the United States. The group says,”Most importantly we want to get the word out about Fosamax, and long term users, who have suffered from an unexplainable broken femur, or broken leg. At the same time, we want to make certain all Fosamax users, who suffered an unexplained broken femur, or thigh bone get to the actual trial law firms or attorneys, that have the best record in achieving superior results for their clients–period.” For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

MDL No. 2243″”In re: Fosamax (Alendronate Sodium) Products Liability Litigation (No. II)

news.yahoo.com

US Drug Watchdog Expands Its National Initiative Involving the Osteoporosis Drug Fosamax and Women Who Suffered Femur or Thighbone Fractures

PRWeb – Tue, Sep 6, 2011

The US Drug Watchdog is dramatically expanding its national initiative involving the osteoporosis drug called Fosamax, and women who may have suffered out of the blue fractures to their femur, or thigh bone. According to the FDA, "typically these fractures occurred after using Fosamax for five years, or more." The US Drug Watchdog says, "In the instance of Fosamax, we are talking about women, whose leg simply broke. They did not fall, they did not run into something, their femur bone simply broke. We need to identify every woman in the United States, who had been using Fosamax for at least five years, and then for some unexplained reason, they suffered a broken femur, or what is called a atypical thigh fracture." Women, who have used the osteoporosis drug Fosamax for more than five years, and then suffered an unexplained broken femur, or thigh bone are encouraged to contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) September 06, 2011

The US Drug Watchdog says,"We are dramatically increasing our efforts with respect to identifying women, who have used the osteoporosis drug called Fosamax, for five years, or more, and then for no apparent reason suffered a broken femur, or thigh bone. One of the biggest problems we have with respect to our drug initiative work, is the average US consumer never hears about a drug recall, or serious side effects related to a specific drug's use. These type of leg breaks are also called atypical fractures.The fracture can happen suddenly and without warning, so this could be a particularly serious Fosamax side effect." On February 3rd 2011, The Journal of the American Medical Association (JAMA) came out with a Canadian medical study that points to a higher risk of a certain type of thighbone fracture in women who take bisphosphonates such as Fosamax for long periods. The US Drug Watchdog wants to hear from any woman, who was using the osteoporosis drug Fosamax for five years, or more, and then suffered an unexplained femur break, also known as a thighbone break. For more information please contact the US Drug Watchdog at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

Other Issues Associated With Fosamax May Include:

• Osteonecrosis of the Hip
• Osteonecrosis of the Jaw
• Osteonecrosis of the Knee
• Osteonecrosis of the Shoulder

The US Drug Watchdog is the premier private pharmaceutical watchdog, and advocacy group in the United States. The group says,"Most importantly we want to get the word out about Fosamax, and long term users, who have suffered from an unexplainable broken femur, or broken leg. At the same time, we want to make certain all Fosamax users, who suffered an unexplained broken femur, or thigh bone get to the actual trial law firms or attorneys, that have the best record in achieving superior results for their clients--period." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

MDL No. 2243—In re: Fosamax (Alendronate Sodium) Products Liability Litigation (No. II)

The US Drug Watchdog Says It's Vital We Identify All Mothers Whose Baby Has A Serious Birth Defect If They Were Using Prozac or Zoloft While Pregnant

Monday, August 1, 2011

The US Drug Watchdog says,"Selective serotonin reuptake inhibitors, better known as SSRI's, are used as an antidepressant. SSRI Antidepressants have a known link to birth defects when taken while pregnant. Some of the more popular brands of Zoloft and Prozac are included." The group fears potentially thousands of US newborns, or infants could be effected. According to the US FDA, "Taking the anti depresants Prozac, or Zoloft while pregnant can increase the risk of the baby having severe birth defects." The US Drug Watchdog Says, "These birth defects include, Persistent Pulmonary Hypertension of the Newborn (or PPHN). PPHN restricts bloodflow and reduces the amount of oxygen in the blood, and Craniosynostosis - premature closing of sutures between the skull bones in infants, restricting brain growth and development. These birth defects are unbelievably horrible, and we want to identify every victim of these specific birth defects." For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) August 01, 2011

The US Drug Watchdog says, "While new drugs are introduced to improve our lives, you must be informed of possible risks. Unfortunately if you took Prozac or Zoloft while pregnant you may have not been warned of the risk of birth defects. We need to get the word out to all US mothers, who were using Prozac, or Zoloft while they were pregnant, especially if their baby had a severe birth defect." The US Drug Watchdog specifically indicates the following birth defects may apply to babies, whose mothers were using Prozac, or Zoloft while pregnant.

• Rapid Breathing
• Rapid Heart Rate
• Difficulty Breathing
• Bluish Skin
• Heart Murmurs
• Low Blood Oxygen Levels

The US Drug Watchdog Says, "Persistent Pulmonary Hypertension of the Newborn, also known as PPHN can be generalized as the baby's respiration system not adjusting to life outside the womb. As such, PPHN is generally noticed by doctors shortly after birth, but 10-20 percent of babies diagnosed with PPHN die despite treatment. If you took Zoloft or Prozac while pregnant and your child is experiencing any of the following symptoms, they may have PPHN, and we want to hear from you. For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

(Multi District Litigation Case Number 1574)

The US Drug Watchdog Calls Their Yaz Yasmin Birth Control Pill Severe Side Effects Initiative Its Most Important Women's Health Initiative Ever

Mon Jun 13, 9:00 am ET

The US Drug Watchdog is calling its Yaz, Yasmin, or the generic version of these birth control pills called Ocella, their most important women's health care initiative ever. The group says, "If a user of the birth control pills called Yaz, Yasmin, or the generic version Ocella has had a pulmonary embolism, a heart attack, stroke, blood clotting, or other severe medical complications, while taking these birth control pills, we want to know about it. We are hearing horror stories from the United States, Canada, as well as other countries, and we are ramping up our efforts, with respect to this initiative." The group says, "If you, a friend, or a loved one are using birth control pills called Yaz, Yasmin, or their generic version Ocella, and severe side effects have occurred, such as a pulmonary embolism, a heart attack, a stroke, or other severe medical conditions please contact us immediately at 866-714-6466." http://USDrugWatchdog.com

(PRWEB) June 13, 2011

The US Drug Watchdog is the premier private advocacy group in the United States for victims of dangerous pharmaceuticals, or medical devices. The group has launched a robust initiative aimed at discovering women who have suffered severe medical side effects while taking Yaz, Yasmin, or Ocella birth control pills. As a background, in September of 2009, the US FDA released a warning letter sent to Bayer Pharmaceuticals over Yaz & Yasmin. The letter indicates that the drug maker hid out-of-specification test results for key ingredients in the birth control pills, and said that several batches of the drugs should have never been released to the public. According to the US Drug Watchdog, "The FDA has also blasted the drug maker for failing to highlight the risk factors associated with these birth control pills. These risk factors, or severe side effects include heart attacks, strokes, blood clotting, gallbladder issues, and other serious medical issues." If a user of the birth control pills called Yaz, Yasmin, or Ocella has had a Pulmonary embolism, a heart attack, stroke, blood clotting, or other serious medical issues, they should contact the US Drug Watchdog immediately at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

The US Drug Watchdog says the following side effects have been associated Yaz, Yasmin, or Ocella:

• Yaz / Yasmin Stroke or Heart attack
• Yaz / Yasmin Pulmonary Embolism
• Yaz / Yasmin Deep Vein Thrombosis
• Yaz / Yasmin Gallbladder Problems (i.e. gallbladder disease or removal)
• Sudden Death from Yaz or Yasmin

The US Drug Watchdog is saying,”We want to talk with users of the birth control pills called Yaz, Yasmin, or the generic version Ocella, if they have had any type of severe medical side effects, or, who have suddenly developed an unexplained severe medical condition. We want to get the word out to all women about these drugs, because of the potential for heart attacks, strokes, and or other serious medical issues, and time really is of the essence. All women include the mother of any potential victim.” The group will find the absolute best lawyers to help Yaz, Yasmin, or Ocella victims in the United States prosecute their claims against this drug maker. For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

MDL No. 2100 (3:09-md-02100-DRH-PMF)

US Drug Watchdog Says It's Vital All ASR DePuy Hip Implant Recipients Understand The Most Common Signs of a Hip Implant Failure

Mon Jun 13, 9:00 am ET

The US Drug Watchdog says, "ASR DePuy hip implants are failing, or have failed at an unacceptably high rate. As a result there was a recall on this hip implant device in August of 2010. The ASR DePuy hip implants were surgically implanted on tens of thousands of US citizens between 2005 and early 2010." Symptoms of a recalled ASR DePuy hip implant failure include pain in the hip region, problems walking, swelling of the hip, or lack of flexibility in the area of the hip. The group says, "Many US citizens who received an ASR DePuy hip implant have been sent a letter by the device maker offering to pay their insurance co-pay? We say, if you received a recalled ASR DePuy hip implant, you are probably owed much more than a insurance co-pay, and we will try to help you find the best possible law firm to help you." The US Drug Watchdog says, "If you, or a loved one has had a hip replacement involving the recalled ASR DePuy hip implant, please call us immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) June 13, 2011

The US Drug Watchdog says, "Because many individuals who received a ASR DePuy hip implant do not want to go through a painful hip replacement surgery, also called revision surgery, they do not complain. Because of this, we are strongly encouraging family members or loved ones of anyone receiving a hip implant between 2005 and early 2010 to ask if it was a ASR DePuy hip implant." They say, "even more worrisome to us is the fact that the ASR DePuy hip implant was sold as the right hip implant for younger adults who wanted to have an active or athletic lifestyle." The group says, "We could have tens of thousands of ASR DePuy hip implant victims in the US, and because of age, or not wanting to go through a hip replacement revision surgery again, they say nothing. Nothing is more important to us than trying to get them some help." For more information about the DePuy hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com.

The US Drug Watchdog indicates symptoms of the recalled ASR DePuy hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier private pharmaceutical watchdog in the United States. The group says, "Tragically the Internet is loaded with misleading ads about ASR DePuy hip implant compensation, lawsuits, or class actions; unfortunately most of the attorneys or law firms advertising for help with the ASR DePuy hip implant failures are middlemen marketing law firms--not the actual trial law firms that will prosecute these cases." They say, "We want to make certain all ASR DePuy hip implant victims get to the actual trial law firms or attorneys that have the best record in achieving superior results for their clients--period--no middleman marketing law firms, or attorneys." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com.

Ohio Southern Federal District Court Case Number MDL No. 2197

The US Drug Watchdog Says It's Yaz Yasmin Birth Control Pill Initiative is Producing Side Effect Horror Stories We Never Thought Possible

• tweet0
• Email
• Print

PRWeb – Wed, Jun 1, 2011

According to the US Drug Watchdog, “We received an e-mail from a young woman's mother on May 26th that said, my 21 year old daughter suffered a massive left middle cerebral artery storke in June of 2010. She has been seen by 11 doctors and it was confirmed by a doctor, that the stroke was generated in the heart and travelled to the brain, and may have been caused by Yasmin birth control pills." The US Drug Watchdog is repeating, "Our Yaz, Yasmin, or generic version Ocella birth control pill initiatives are now officially our most important women's health initiative ever. We are also very focused on women who used Yaz, Yasmin, or Ocella, and subsequently had their gallbladder removed, or developed other severe medical complications." The group says, "If you, or a friend are using birth control pills called Yaz, Yasmin, or their generic version Ocella, and severe side effects have occurred, such as severe gallbladder issues, a pulmonary embolism, a heart attack, a stroke, or other severe medical conditions please contact us immediately at 866-714-6466." http://USDrugWatchdog.com

(PRWEB) June 01, 2011

The US Drug Watchdog is the premier private advocacy group in the United States for victims of dangerous pharmaceuticals, or medical devices. The group says, "We are receiving e-mails from mothers, or loved ones of young women who used the birth control pills called Yaz, Yasmin, or the generic version called Ocella that sound like this; My 21 year old daughter suffered a massive Left middle cerebral artery storke in June of 2010. She has been seen by 11 doctors and it was confirmed by the one of the doctors, that the stroke was generated in the heart and travelled to the brain may have been caused by Yasmin birth control pills." The group is expanding its initiative related to the birth control pills called Yaz, Yasmin, and the generic version called Ocella. The group says, "If a user of the birth control pills called Yaz, Yasmin, or the generic version Ocella has had gallbladder problems, a pulmonary embolism, a heart attack, stroke, blood clotting, or other serious medical issues, they should contact the US Drug Watchdog immediately at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

The US Drug Watchdog says the following side effects have been associated Yaz, Yasmin, or Ocella:

• Yaz / Yasmin Stroke or Heart attack
• Yaz / Yasmin Pulmonary Embolism
• Yaz / Yasmin Deep Vein Thrombosis
• Yaz / Yasmin Gallbladder Problems (i.e. gallbladder disease or removal)
• Sudden Death from Yaz or Yasmin

The US Drug Watchdog is saying,”We want to talk with users of the birth control pills called Yaz, Yasmin, or the generic version Ocella, if they have had any type of severe medical side effects, or, who have suddenly developed an unexplained severe medical condition. We want to get the word out to all women about these drugs, because of the potential for heart attacks, strokes, and or other serious medical issues, and time really is of the essence.” The group will find the absolute best personal injury law firms to help these Yaz, Yasmin, or Ocella victims prosecute their claims against this drug maker. For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

MDL No. 2100 (3:09-md-02100-DRH-PMF)

The US Drug Watchdog Calls Its Yaz Yasmin Birth Control Pill Initiative Its Most Important Women's Health Campaign Ever

According to the US Drug Watchdog, “We received an e-mail from a young woman on Saturday May 21st, who after taking the birth control pill called Yaz, she developed a pulmonary embolism, and nearly died. Our Yaz, Yasmin, or generic version Ocella birth control pill initiative is now officially our most important women's health initiative ever. We are also very focused on women who used Yaz, Yasmin, or Ocella, and subsequently had their gallbladder removed, or developed other severe medical complications." The group says, "If you, or a friend are using birth control pills called Yaz, Yasmin, or their generic version Ocella, and severe side effects have occurred, such as severe gallbladder issues, a pulmonary embolism, a heart attack, a stroke, or other severe medical conditions please contact us immediately at 866-714-6466 or http://USDrugWatchdog.com.

(PRWEB) May 24, 2011

The US Drug Watchdog is the premier private advocacy group in the United States for victims of dangerous pharmaceuticals, or medical devices. The group is expanding its initiative related to the birth control pills called Yaz, Yasmin, and the generic version called Ocella. The group says, "We are dramatically expanding our ongoing national investigation of the birth control pills called Yaz, Yasmin, and Ocella, over concern that the use of these drugs could be associated with serious gallbladder issues, pulmonary embolisms, strokes, heart attacks, blood clots, and other very serious health side affects.” They say, "We just spoke with a young woman, who had a pulmonary embolism after only taking Yaz for several months." If a user of the birth control pills called Yaz, Yasmin, or the generic version Ocella has had gallbladder problems, a pulmonary embolism, a heart attack, stroke, blood clotting, or other serious medical issues, they should contact the US Drug Watchdog immediately at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

Possible Side Effects Yaz/Yasmin

• Yaz / Yasmin Stroke or Heart attack
• Yaz / Yasmin Pulmonary Embolism
• Yaz / Yasmin Deep Vein Thrombosis
• Yaz / Yasmin Gallbladder Problems (i.e. gallbladder disease or removal)
• Sudden Death from Yaz or Yasmin

The US Drug Watchdog is saying,”We want to talk with users of the birth control pills called Yaz, Yasmin, or the generic version Ocella, if they have had any type of severe medical side effects, or, who have suddenly developed an unexplained severe medical condition. We want to get the word out to all women about these drugs, because of the potential for heart attacks, strokes, and or other serious medical issues, and time really is of the essence.” For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

The US Drug Watchdog Expands Its Yaz Yasmin Birth Control Pill Investigation Focused on Gallbladder Issues, Heart Attacks & Strokes

Monday, May 16, 2011

The US Drug Watchdog is expanding its national investigation of the birth control drugs called Yaz and Yasmin given increasing evidence these drugs may be responsible for serious gallbladder issues, Pulmonary embolism's, deep vein thrombosis, heart attacks, strokes and other serious side affects with users. The Food and Drug Administration (FDA) cited Bayer in 2009 for running misleading television commercials, and for not following proper quality-control procedures at a plant that makes hormone ingredients. According to the US Drug Watchdog, "Our initiative effects millions of US women, and we want to hear from any Yaz, or Yasmin user, or loved ones, if the user had a heart attack, stroke, blood clotting, or any other serious medical issue." Yaz, or Yasmin users can call the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via its web site at http://USDrugWatchdog.Com

(PRWEB) May 16, 2011

According to the US Drug Watchdog, "We are expanding our ongoing national investigation of the birth control pills called Yaz, Yasmin, and Ocella, over concern that the use of these drugs could be associated with serious gallbladder issues, strokes, heart attacks, blood clots, and other very serious health side affects." The FDA released a warning letter sent in mid September 2009 to Bayer Pharmaceuticals over Yaz & Yasmin. The letter indicates that the drug maker hid out-of-specification test results for key ingredients in the birth control pills, and said that several batches of the drugs should have never been released to the public. According to the US Drug Watchdog, "The FDA has also blasted the drug maker for failing to highlight the risk factors associated with the drug. These include heart attacks, strokes, blood clotting, gallbladder issues, and other serious medical side effects." If a user of the birth control pills called Yaz, or Yasmin has had gallbladder problems, a Pulmonary embolism, a heart attack, stroke, blood clotting, or other serious medical issues, they should contact the US Drug Watchdog immediately at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

What is the difference between Yaz & Yasmin?

According to the US Drug Watchdog," the only difference between the two pills is that the estradiol in Yaz is lower than in Yasmin. but it is not the estradiol that causes most problems, it is the type of progesterone called drosperinone. The amount of drosperinone is the same in both of the pills." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

Possible Side Effects Yaz/Yasmin

• Yaz / Yasmin Stroke or Heart attack
• Yaz / Yasmin Pulmonary Embolism
• Yaz / Yasmin Deep Vein Thrombosis
• Yaz / Yasmin Gallbladder Problems (i.e. gallbladder disease or removal)
• Sudden Death from Yaz or Yasmin

The US Drug Watchdog is saying,"We want to talk with potential medical side affect victims of the birth control pills called Yaz, or Yasmin. We want to get the word out to all women about these drugs, because of the potential for heart attacks, strokes, and or other serious medical issues, and time really is of the essence." For more information please call the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

MDL No. 2100 (3:09-md-02100-DRH-PMF)

US Drug Watchdog Urges All ASR DePuy Hip Implant Victims to Get Identified and Lists the Most Common Symptoms of a Hip Implant Failure

The US Drug Watchdog says, "It is critical we identify all US recipients of the recalled ASR DePuy hip implant. These artificial hips were surgically implanted on tens of thousands of US citizens between 2005 and early 2010. The ASR DePuy hip implant has been recalled because of a much higher than normal failure rate." Symptoms of a recalled ASR DePuy hip implant failure include pain in the hip region, problems walking, swelling of the hip, or lack of flexibility in the area of the hip. The group says, "Many US citizens who received an ASR DePuy hip implant were sent a letter by the device maker offering to pay the insurance co-pay. We say, if you received a recalled ASR DePuy hip implant, you are probably owed much more than a insurance co-pay, and we will try to help you find the best possible law firm to help you." The US Drug Watchdog says, "If you, or a loved one has had a hip replacement involving the recalled ASR DePuy hip implant, please call us immediately at 866-714-6466." http://USDrugWatchdog.Com

(PRWEB) May 10, 2011

The US Drug Watchdog says, "Our recalled ASR DePuy hip implant victim identification initiative is the most complicated campaign we have ever been involved with. One of our biggest problems is individuals who received a recalled ASR DePuy hip implant may not want to complain, because they don't want to go through hip replacement surgery again. Because of this, we are strongly encouraging family members, or loved ones of anyone receiving a hip implant between 2005 and early 2010 to ask if it was a ASR DePuy hip implant." The group says, "We could have tens of thousands of ASR DePuy hip implant victims in the US, and because of age, or not wanting to go through a hip replacement revision surgery again, they say nothing. Nothing is more important to us than trying to get them some help." For more information about the DePuy hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

Symptoms of the recalled ASR Depuy hip implant failure include:

• Pain in the Hip Region
• Problems While Walking or The Inability to Walk
• Swelling of the Hip
• General Discomfort
• Lack of Flexibility

The US Drug Watchdog is the premier private pharmaceutical watchdog in the United States. The group says, "Tragically the Internet is loaded with misleading ads about ASR DePuy hip implant compensation, lawsuits, or class actions; unfortunately most of the attorneys or law firms advertising for help with the ASR DePuy hip implant failures are middlemen marketing law firms--not the actual trial law firms that will prosecute these cases." They say, "We want to make certain all ASR DePuy hip implant victims get to the actual trial law firms or attorneys that have the best record in achieving superior results for their clients--period--no middleman marketing law firms, or attorneys." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.Com

Ohio Southern Federal District Court Case Number MDL No. 2197