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Nationwide Testosterone Lawyers For Heart Attack and Stroke Victims


Nationwide Testosterone Lawsuit Attorney Network


Get A  Testosterone Lawsuit  Lawyer  Handling Testosterone Heart Attack and  Stroke Lawsuits

If you or a loved one suffered from a heart attack or stroke while using AndroGel you may be entitled to damages. We provide free no-obligation Atlanta testosterone lawsuit case review. We do not charge attorney fees unless you receive compensation and you are under no obligation after your initial consultation.

Testosterone Therapy May Raise Heart Attack Risks

Researchers say risk of heart attack doubles after treatment starts for men under 65 with heart problems and all men over 65.

Nationwide  AndroGel  Lawsuit Attorneys
Testosterone Stroke and Heart Attack

AndroGel® (testosterone gel)  is a daily testosterone replacement therapy  that can help bring T levels back to normal with daily use.

FDA Is  Investigating Potential  Heart Attacks And  Strokes From Testosterone Products

On Jan. 31, 2014, the  FDA announced  it would be investigating the risk of heart attacks, strokes and possible  deaths in men using  testosterone products. The FDA made this announcement after reviewing the study conducted at the National Cancer Institute, as well as the study published in JAMA. The FDA recommended the health care practitioners should  consider the benefits of testosterone treatment and potential the  risks.

If you or a loved one has had a stroke or heart attack after using testosterone therapy call now and get connected to one of our experienced testerone lawyers

 

 

 

 

 

Januvia, Byetta Risks of Pancreatic Cancer, Lawyers Looking At Lawsuits

New Information on Byetta and Januvia is gaining interest by lawyers for Pancreatic and Thyroid Cancer. Type II Diabetics are potential victims of cancer from these Diabetic drugs.

Popular diabetes drugs may raise pancreatic cancer risk, study suggests
By Steven Reinberg, HealthDay
Updated 9/23/2011 6:15 PM

People with type 2 diabetes taking the drugs Januvia or Byetta might have an increased risk of developing pancreatitis and pancreatic cancer, a preliminary study suggests.
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The study also found that Byetta (exenatide) may raise the risk of thyroid cancer.

Although the links aren't conclusive, they merit further investigation, the researchers noted.

"We have raised concern that there may be a link, but we haven't confirmed it," said lead researcher Dr. Peter Butler, director of the Larry L. Hillblom Islet Research Center at the University of California, Los Angeles. "We need to do more work to figure out whether this is real or not."

Both drugs help control blood sugar levels by encouraging production of a hormone called glucagon-like peptide 1 (GLP-1).

Januvia (sitagliptin) and Byetta, an injectable drug, are a new way of treating type 2 diabetes, and they potentially have advantages over older medications, Butler said. But, because these drugs are new, they're "the ones we know least about," he said. "When new drugs come out, the long-term side effects of these drugs are not well understood."

For the study, recently published in the journal Gastroenterology, Butler's team used 2004-2009 information in the U.S. Food and Drug Administration's database on adverse events, which are reported by doctors whose patients use these drugs.

When compared to other treatments, the researchers found a sixfold increase of reported cases of pancreatitis (inflammation of the pancreas) linked to patients taking Januvia or Byetta; a 2.9-fold increase in reported cases of pancreatic cancer among those taking Byetta and a 2.7-fold increase of reported pancreatic cancers among Januvia users.

In addition, they also noted an increase in reported cases of thyroid cancer with Byetta.

This latest study builds on earlier research, published in a 2009 issue of Diabetes, which found an increase in pancreatitis in rats whose GLP-1 levels were raised, the researchers said.

Butler is quick to point out that these increases in pancreatic cancer risk, while statistically significant, are not specifically related to patients, but rather to an increase in doctors reporting these cases to the FDA.

"It is important to avoid alarmism and have people stop medicines that they may be benefitting from when the risk is not yet defined," he stressed.

"If the drug and you are working well together, I wouldn't say there is any reason to stop the drug, based on the evidence we have right now," he said. "But if you have any concern you should talk to your doctor about it."

Being overweight is an important risk for both pancreatic cancer and type 2 diabetes, Butler noted. So the first advice to overweight patients with type 2 diabetes is to lose weight. "By doing that, you reduce the risk of pancreatic cancer," he said.

In addition, the first medication used to control blood sugar in type 2 diabetics is metformin, which by itself may reduce the risk for pancreatic cancer, Butler said. Metformin is an older drug with a well-known safety profile, he noted.

Dr. Mary Ann Banerji, director of the Diabetes Treatment Center at SUNY Health Science Center Brooklyn in New York City, said that "this is not perfect data."

However, Banerji does not prescribe these drugs for patients who have had a history of pancreatitis or a family history of thyroid cancer. There are alternatives such as metformin and insulin, as well as Avandia and Actos, she said, but studies have turned up an increased risk for heart attack and heart failure in the last two drugs. The FDA has removed Avandia from pharmacy shelves, and the agency issued a warning last summer that there is a possible increased risk of bladder cancer in patients who take Actos for more than a year.

The concerns about Januvia and Byetta "should not be blown out of proportion," Banerji said. "You prescribe them on an individual basis, because, in the end, all of medicine is individual," she said. "We should use these drugs judiciously along with metformin."

Industry representatives, insisting that no studies involving these drugs have found an increased risk of pancreatitis or pancreatic cancer, stand by their products. The database used for the study contains information on doctor-reported cases and does not reflect cause-and-effect, they said.

Dr. Barry Goldstein, vice president and therapeutic area head for diabetes and endocrinology at Merck Research Laboratories, which makes Januvia, said that "there has been no association shown between Januvia and pancreatitis."

"We have full confidence in Januvia, which is used by millions of patients around the world," he said.

Anne Erickson, a spokeswoman for Amylin Pharmaceuticals, makers of Byetta, said that "the conclusions of the study are in contrast to other nonclinical, clinical and adequately conducted post-marketing epidemiological studies."

Epidemiological studies have not established a significantly increased risk of pancreatitis associated with Byetta, she said. "To date, the available data do not demonstrate that exenatide increases the overall risk of cancer in humans."

Another expert, Dr. Ronald Goldberg, professor of medicine, biochemistry and molecular biology at the University of Miami Miller School of Medicine, said the findings merit consideration. "I don't think the study is definitive, but it raises a flag and is clearly something we need to pay attention to going forward."

There is "more benefit than risk with these drugs, based on our current knowledge," he

Fosamax Lawyers for Women Injured By Fosamax, Femur Fractures

Fosamax Femur Fracture Lawyers

Our Fosmax lawyers are filing lawsuits for Femur faracture from Fosmax.

Fosamax (alendronate) is a part of the class of bisphosphonates. Fosamax  alters the cycle of bone formation and breakdown in the body. Fosamax slows bone loss while increasing bone mass, which may prevent bone fractures.

Fosamax is used in men and women to treat or prevent osteoporosis that is caused by menopause or by taking steroids. Fosamax is also used to increase bone mass in men who have osteoporosis, and to treat Paget's disease of the bone in men and women.

However, Fosamax has been a central focus of lawsuits.  Fosamax has been linked to a number of severe side effects that has required many revisions of the Fosamax Warning label.  These side effects have brought about a wide range of Fosamax lawsuits. Fosamax has been shown to cause Osteonecrosis of the Jaw Injury, Femur Fractures, and Severe Musculoskeletal Pain.

FDA Issues Fosamax Warning

On Oct. 13, 2010, the U.S. Food and Drug Administration issued a Fosamax safety about the risk of atypical femur fractures. The victims of Fosamax are mostly  post menapausal women who lose bo have osteoporosis due to loss of estrogen.  Fosamax has caused what it was prescibed to help, femur fractures.

Reports from the Hospital for Special Surgery and Columbia University Medical Center have reported  that Fosamax changes bone remodeling in an unknown manner and may contribute to Fosamax Femur Fractures.  Many medical journals have reported Femur faractures from Fosamax. According to the geriatric social worker who runs the helpline" Our concern is with the elderly who have been prescibed Fosamax. Femur fractures heal slower as we age and usually require long periods of rehabilitation and physical therapy."

The femur is one of the largest, and strongest bones in the body. The femur is the thigh bone. The femur extends from the hip joint down to the knee joint. Because the femur is such a strong bone, it can take tremendous force to cause a femur fracture. Spontaneous femur bone fractures are extremely unusual and  serious for anyone but, especially serious for older women."

For the most part Femur fractures are caused by extremely high impact accidents like car accidents or   Falls from a height although they can happen to the fragile elderly from a fall.

It is interesting to note  that womwn may also have bone that is weakened by osteoporosis thae exact medical condition Fosamax was to help.

Femur fractures include:

  •         Hip Fractures
  •         Femoral Neck Fractures
  •         Intertrochanteric Femur Fractures

Femur fractures almost always require surgery and long periods of rehabilitation and Physical therapy. Sometimes they result in a length variatopn due the a potential hip rotation during surgery and cam lead to poor balance. In some cases the pre- fracture level of functioning does not return completely.

Fosamax MDL Update

All Fosamax lawsuits alleging that  the victim  sustained an atypical femur fracture as a result of taking the bisphosphonate Fosamax, can also include victims who took similar medications such as Reclast or Boniva as long as they did, in fact, take Fosamax.

If you a family member or someone you are a caregiver for has a spontaneous femur fracture and is on one of these medications contact our Fosamax Helpline to find out if you can be included in the current Fosamax litigation underway.

Current Fosamax News

 A U.S. District Court judge has  ordered  hundreds of  Fosamax lawsuits returned to the state courts and out of the MDL.Judge John Keenan ordered that 200 Fosamax  cases a month be returned to the state  courts where they were filed.

 

Florida Unpaid Time and Half Claims, Unpaid Overtime Lawyers

If you have not been paid time and a half in Florida for overtime worked you may have a wage and hour claim against your employer.  You deserve to get paid according to Florida law for the hours you put in. You may have a class action lawsuit for unpaid wages. Our lawyers for unpaid wages offer legal help for:

  •     Lawyers for time and a half pay for overtime,
  •     Lawyers for Fair Labor Standards Act,
  •     Labor Emplyment Lawyers ,
  •     Class actions  for Unpaid Overtime Wages,
  •     Lawyers for Wage and Hour Claims,
  •     Lawyers for FLSA and Unpaid Commissions,

Overtime pay of time and a half is due once an employee has worked forty (40) hours in a work week.

 The Fair Labor Standards Act (“FLSA”)  

The FLSA establishes the rules for  governing employees’ rights to minimum wage and overtime pay which include:

  • Time and a half wages for employees for all hours over 40 worked in a workweek.
  •  A minimum wage of at least $7.25 for all hours worked.

What can I expect if I win a wage and hour claim against my employer?

  • Back pay for all unpaid overtime, beginning two (2) years before the lawsuit is filed.
  • Double the amount of unpaid wages, in some instances
  • Your employer will be liable for the attorneys fees

 

For the full details about your Florida unpaid wages, to file an unpaid wages claim and to see if you have a claim for unpaid overtime call our wage and hour claim hotline today

In Florida you deserve to get paid your full WAGES FOR HOURS WORKED and all overtime back pay for unpaid wages claims.

GranuFlo Lawyers, NaturaLyte Lawsuits

 

Fresenius Medical is the manufacturer of  GranuFlo and NaturaLyte acid concentrate. These are drugs used in  dialysis treatment. There has been a recall of these dialysis drugs and  lawsuits are being filed.

Injury and death has resulted from these drugs:

  •  GranuFlo cardiovascular death,
  •  GranuFlo sudden cardiac death,
  •  GranuFlo cardiopulmonary arrest,
  •  GranuFlo heart attack,
  •  GranuFlo catastrophic cardiovascular injuries

 

Fresenius manufactures GranuFlo and NaturaLyte used in dialysis. These drugs cause alkalosis, a condition associated with an increase in cardiovascular fatalities.

 

The FDA received complaints describing alkali dosing errors that occurred during hemodialysis using dialysate concentrates containing acetic acid and acetate. When metabolized, these potential sources of alkali can contribute to elevated bicarbonate levels in patients undergoing hemodialysis.

 

This can contribute to metabolic alkalosis, which is a significant risk factor associated with :

 

Low blood pressure

Cardiopulmonary arrest

Cardiac arrhythmia

Sudden heart attack

Stroke

Hemodialysis cardiopulmonary arrest

 

A study which was conducted between January and December of 2010 found that patients with pre-dialysis bicarbonate levels greater than 28mEq/L were 4.7 times more likely to suffer a cardiac arrest. The study also discovered that patients with pre-dialysis potassium lower than 4 mEq/L had a 6.3 times higher risk of cardiac arrest.

 

In May 2012 the FDA notified health care providers to consider the presence and quantity of acetate, citrate, and/or acetic acid in dialysate concentrates when determining the patients’ dialysate prescription.

There is a GranuFlo and NaturaLyte Class 1 Recall

 

Serial numbers for recalled Naturalyte Liquid Acid Concentrate range from:

 

08-0231-4, 08-1001-0, 08-1201-8, 08-1231-3, 08-1251-1, 08-1301-4, 08-2201-5, 08-2231-2, 08-2251-0, 08-2301-3,08-2351-8, 08-3201-4, 08-3231-1, 08-3251-9, 08-3301-2, 08-4123-1, 08-4223-7, 08-4225-1, 08-4230- 2, 08-4231-0, 08-4323-5, 08-4325-1, 13-1251-1, 13-2201-5, 13-2231-2, 13-2251-0, 13-3231-1, 13-3251-9, 13-4123-1, 13-4220-1, 13-4225-1, 13-4325-

 

Serial numbers for recalled Naturalyte GranuFlo (powder) Acid Concentrate range from:

 

OFD1201-3B, OFD1251-3B, OFD2123-3B, OFD2201-38, OFD2220-3B, OFD2223-3B, OFD2225-3B, OFD2231-3 B, OFD2251-3B, OFD2301-3B, OFD2323-3 B, OFD2325-3B, OFD3201-3B, OFD3231-3B, OFD3251-3B, OFD3301-3B

GranuFlo & NaturaLyte is one of the most widely prescribed dry acid products used for dialysis  at Fresenius'  clinics, as well as other hemodialysis centers that purchase their dialysis supplies from Fresenius.  It is estimated that 125,000 patients in non-Fresenius clinics are treated with GranuFlo.

Dilaysis Patient Alert

If you, a loved one or someone you care for has been injured by these products contact us for a GranuFlo and NaturaLyte lawsuit.

Bladder Sling Lawyers, Vaginal Mesh Lawsuits

The bladder mesh is a vaginal mesh product primarily used for urinary incontinence. This mesh sling has caused severe complications and bladder mesh lawyers are filing lawsuits. Many women with a bladder mesh do not realize they are eligible to file a vaginal mesh lawsuit.

What is a Bladder Sling?

Urethral sling or bladder sling  is used  to treat urinary incontinence by placing a sling around the urethra to lift it back into a normal position and to exert pressure on the urethra to aid urine retention. The sling is attached to the abdominal wall. A bladder sling is a mesh device and is part of the vaginal mesh litigation. The complications of a failed bladder sling is increased incontinence or trouble voiding. Many women have needed to self catherize.

 Bladder Sling Complications?

According to the July 2011 FDA news release, the most common complications associated with surgical mesh bladder slings is erosion thru the vaginal wall or into the bladder, pain during sexual intercourse, bleeding, infection, perforation of various pelvic organs (bladder, colon, vaginal walls), and urinary incontinence or problems voiding as well as; neuromuscular problems, emotional problems, mesh contraction/shrinkage, and even a reoccurrence of POP and/or SUI.

Bladder sling lawsuits are being filed on a contingency fee basis against the mnaufacturers of the bladder sling:

        Bard Avaulta Support System
        AMS Elevate Prolapse Repair System
        AMS Apogee Vault Suspension System
        AMS Perigee System
        AMS Monarc Sling System
        AMS Sparc Sling System
        Ethicon Gynecare Gynemesh
        Ethicon Gynecare Prolene Soft Mesh
        Ethicon Gynecare Prolift Pelvic Floor Repair System
        Ethicon Gynecare TVT Transvaginal Sling
        Boston Scientific Pinnacle Pelvic Floor Repair Kit
        Boston Scientific Uphold Vaginal Support System
        UGYTEX Dual Knit Mesh
        Coviden IVS Tunneler Sling

Contact us today.

Stryker Hip Replacement Lawyers, Stryker Hip Replacement Helpline

Adding to the Zimmer and DePuy metal on metal hip replacement Stryker has recalled it's latest metal component hip replacement implant.  Stryker has voluntarily recalled the  Rejuvenate metal component hip replacement implant and ABG II modular- neck stems
Stryker has voluntarily  stopped  market distribution of these hip replacements due to  increased risk of injury. The hip replacement implants have been shown to fret or corrode, harming body tissue and causing pain and  swelling. Other injuries include:

  •     Severe inflammatory reactions
  •     Pain in the groin
  •     metal toxicity ort poisoning
  •     high metal levels in the blood
  •     need for additional surgery
  •     Breakdown of muscles, tendons and other soft tissues in and around the hip joint
  •     Loss of surrounding bone
  •     Loss of mobility

While other types of hip implants such as those made by Johnson & Johnson and DePuy Orthopaedics Inc. involve a metal ball rubbing against a metal socket, the Stryker Rejuvenate products involve a metal neck inside a metal stem. The Stryker Hip replacement Helpline and  hip replacement lawyers are reaching out to all victims of the failed device for a potential multi district litigation.

The products have metal components and although they are not metal on metal run the same risks of chromium and cobalt toxicity poisoning. If you have been injured you are advised to contact your doctor immediately and contact the Stryker Hip Replacement Helpline for a Stryker lawyer

Attention DePuy Hip Replacement Lawsuit Filing Ending August 2012

Breaking news; If you were injured by the DePuy hip Recall You must file your lawsuit now. Filing deadline August 2012

Most DePuy ASR Lawsuits Must Be Filed Before August 2012

Posted May 18, 2012 4:57 PM

 
DePuy ASR hip implant patients in most states who do not file lawsuits before August 23, 2012 may lose their rights to compensation or to file a lawsuit. Every state has a law called the statute of limitations that sets a limited time period in which a lawsuit for compensation can be filed. If a person with a legal claim or legal case fails to have a lawsuit filed on their behalf within this time period their claim can be forever barred. In summary, people who do not assert their rights in court within a limited time lose those rights and can never thereafter bring that claim.
Why is the Statute of Limitations for Most ASR Hip Implant Patients This August?
Every state has its own time limit for filing lawsuits called the Statute of Limitations. DePuy and Johnson and Johnson, the manufacturers of the ASR Hip Implant, have a right to have lawsuits dismissed or decided in their favor regardless of the injuries if the lawsuit is not filed in time to comply with the statute of limitations.
Most states in the United States use a two year time period for the statute of limitations. Other states may have a 1 year up to a six year time period for the statute of limitations. Different states use different rules to calculate when these time periods start running and when it is too late to bring a lawsuit. These calculations can be difficult to make and there have been many lawsuits over the running of the statutes of limitations in different types of cases. Each person’s case should be carefully evaluated individually by an experienced lawyer because individual circumstances can affect calculating this time period. This blog is for general information and awareness and you should not use this information to make your own calculation to rely on for your case for the statutes of limitations.
This two year statute of limitations will run for many DePuy ASR hip implant cases because the official DePuy Recall Notice that received widespread publicity was issued on August 24, 2010. The two year period from that Recall Notice will expire on August 23, 2012. Thus, lawsuits for injured ASR patients must be filed in those states with a two year statute of limitations or it may be too late for those patients to make a claim.
Which States Have a Two Year Statute of Limitations
Arizona, Alabama, Alaska, California, Colorado, Connecticut, Delaware, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, North Dakota, New Jersey, Ohio, Oklahoma, Oregon, Pennsylvania, Texas, Utah, Virginia, and West Virginia are the states with a two year statute of limitations for injury cases.
However, the calculations used to measure the two year time periods are different in different states and it is important to have each case calculated by an experience attorney to be sure that the time period does not run out before the lawsuit is filed.
For example, the two year statute of limitations in Virginia is unusual in that the two year time period in that state runs from when the person first has pain or is aware of an injury even if that was before the recall of before they had any idea that DePuy might be responsible. So in Virginia it is likely that the statute of limitations may have already run on some cases where the person had pain from their hip implant before the recall date. It is possible that someone reading this blog could have a statute of limitations that will run tomorrow or next week!
Immediate individual legal advice is critical to making sure that the Statute of Limitation is not missed.
There are many states other than those listed above that have a statute of limitations of two years from the date of death if the implant caused a death. Some states have longer statutes of limitations for injury cases than for death cases.
Are There Exceptions to the Statute of Limitations?
There are few exceptions to the Statute of Limitations. One of the clearest is the Sailors and Soldiers Relief Act which can toll the statute of limitations for some active members of the military while they are in the service of our country. Tolling of the Statute of Limitations means that the time period is stopped from running. That means that some active military people could wait many years before having to file their cases. Our firm has had other types of cases where the statute of limitations has been tolled for decades while a military person is in active service.
Many states have what is called a “Discovery Rule” which means that the Statute of Limitations does not start until a person would reasonably know that they might have a liability claim. I believe many judges would rule that the widespread public dissemination of the DePuy Recall Notice of August 24, 2010 would start the clock running on the statute of limitations even if an individual person did not hear about it or know about it because the test is usually an objective test about what a reasonably informed person would know.
There is another highly complex legal rule called the “American Pipe Rule” that may be applied in some states if a class action is pending to toll the time period for an individual lawsuit for a person who would be a member of that class action. This theory should not be relied on for DePuy ASR cases because there is no viable class action that I know of. The ASR cases are coordinated for pretrial purposes in a federal multidistrict proceeding called an MDL but this is not a class action and will not toll or stop the statute of limitations from running in an individual case unless an individual case is filed for that person.
Mental incompetence can be an exception in some states that could extend the statute of limitations. For example, someone with severe Alzheimers disease might qualify in some states for an extension to the statute of limitations.
Final Advice on the Statute of Limitations for ASR Lawsuits
Every person with a DePuy ASR Hip Implant should have a detailed review of the statute of limitations done by an attorney experienced in medical product liability cases. This review should be done immediately because once the statute of limitations has run there is no way to reopen or restart it. Once the statute of limitations has run it is too late to ever bring a lawsuit for harms and injuries from the defective ASR metal on metal hip implants.

Hurricane Claims Lawyers, Storm Claims Lawyers

If you have a claim for a Hurricane You need an Experienced  Insurance Bad Faith lawyer Fihting for your rights. Our team of Insurance Claim lawyers are experienced in Florida windstorms, Hurricanes, and tornado damgae claims. You can count on us for Hurricane and windstorm as well as flood claims.Windstorms, Hurricanes Florida Hurricane Insurance Claim Attorneys and Florida Lawyers, helpling with Hurricane Damage claims and  Windstorm Damage Claims.

Windstorms, hurricanes and tornadoes can create massive destruction. When wind damage occurs, it can open the door to complicated ambiguities with insurance coverage during the adjustment process. In the aftermath of a disaster,  you will need help with

  •     Protecting your property.
  •     Getting your business or home back to normal.
  •     Securing adequate financial recovery.
     

As a home owner , business owners and property owners we are faced  with threat of property damage each year from windstorms, tropical storms and hurricanes. Hurricanes in 2004 and 2005 caused tremendous damage to residential and commercial properties in Florida. Property owners often faced insurance companies determined to deny claims or minimize claim payments. While most of these hurricane insurance claims have since been resolved, there is no doubt many victims of future storms will have problems with their insurers..

If you are an individual, business, condo association or homeowner’s association in the state of Florida and have suffered a property loss due to a windstorm or hurricane, we encourage you to contact the experienced insurance law attorneys at Tyler & Hamilton, P.A. To contact our Jacksonville law office, call 904.398.9999, or in Florida call us toll-free at 1.800.344.1122.
Lawyers Protecting Your Rights in Wind Damage Claims in Miami, Ft Lauderdale,Orlando, Jacksonville, Tampa, Ft Myers, Winter haven, ocala Sarasota, West Palm Beach and Throughout Florida. Expanded coverage for storm damage victims in NYC and New Jersey. We know storms. Your best bet is an experinced hurrican damage lawyer.

When a windstorm or hurricane causes your home or business property to sustain water damage, structural damage or other property damage, you have a right to receive the full benefits under your insurance policy. This could include cost of repairs, temporary/alternative residence costs, storage costs, transportation costs and other additional costs incurred due to the windstorm damage.

insurance companies have their own goals. They want to prevent you from receiving the full benefit of your homeowner’s, commercial or commercial, residential insurance policy.
Our Hurricane, Tornado, wind, storm and flood Lawyers will help you Receive  aggressive Representation for your hurricane and Tornado Claims,

The states with most Tornadeos are : Texas, Massachusetts, Oklahoma, Missisppi

States with most hurricanes

 

  • Texas,
  • Louisiana,
  • Mississippi,
  • Alabama ,
  • Florida,, 
  • Georgia,
  • South Carolina,
  • North Carolina,

Pradaxa Breaking News, Pradaxa lawyers, Pradaxa Lawsuits, Pradaxa Bleeding

Pradaxa has warnings for excessive bleeding. Pradaxa Helpline is concerned about Pradaxa and the elderly

The Pradaxa Helpline Has Pradaxa Lawyers to Help You

   LONDON | Fri May 25, 2012 6:07am EDT

(Reuters) – Doctors and patients should be given clearer guidance on how to avoid bleeding risks when using Boehringer Ingelheim's new stroke prevention pill Pradaxa, European regulators said on Friday.

The European Medicines Agency said data continued to confirm the positive benefit-risk balance of the anticoagulant medicine, despite cases of fatal bleeding, but advice on the risks should be strengthened.

Pradaxa is the first in a new class of medicines aimed at replacing the old and problematic drug warfarin. It is designed for use after hip and knee surgery and to prevent strokes in patients with atrial fibrillation, a form of irregular heartbeat common among the elderly.

Rival drugs include Xarelto, from Bayer and Johnson & Johnson, and Eliquis, from Bristol-Myers Squibb and Pfizer.

       Pradaxa is an anticoagulant. Anticoagulants effect the clotting time of the blood. Pradaxa is described as  a prescription blood-thinning medicine used to reduce the risk of stroke and blood clots in people with atrial fibrillation not caused by a heart valve problem. With atrial fibrillation, part of the heart does not beat the way it should. This can cause blood clots to form, increasing your risk of a stroke. Pradaxa lowers the chance of blood clots forming in your body. There is a chnce of excessive bleeding on Pradaxa that can be fatal.

We can locate a Pradaxa lawyer to help you: