Drug Products | InjuryBoard Atlanta

According to recent reports, Zimulti, an obesity drug manufactured by Sanofi-Aventis SA has been linked to an increase in suicidal thoughts in its consumers. Although the drug is not currently being sold in the U.S, an FDA advisory panel is set to discuss Zimulti Wednesday to consider whether its approval should be granted in the states. Known generically as rimonabant, the drug already is sold...

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Issues surrounding GlaxoSmithKline's controversial diabetes drug Avandia continued today in a recent article published by ABCNEWS: Doctor to Testify in Avandia Hearing on Hill. According to reports, Dr. John Buse was contacted by SmithKline Beecham in 1999 after noting an increased trend of heart related problems in patients that were taking Avandia. Dr. Buse was reportedly threatened by the...

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KETEK (telithromycin), manufactured and sold by Sanofi-aventis U.S. recently decided, after prompting by the U.S. Food and Drug Administration, to include a revised black box warning and contraindication for myasthenia gravis patients. The new warning also removed the labels recommendation that KETEK be used in patients with chronic bronchitis (AECB) and acute bacterial sinusitis (ABS). For more...

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The sale of Zelnorm, (tegaserod maleate) approved in 2002 for treatment of irritable bowel syndrome with constipation, has recently been suspended by its manufacturer, Novartis, after the drug has been linked to a significant number of cardiovascular risks. This decision was made after the United State Food and Drug Administration found the drug can lead to increased occurrences of heart attack,...

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The United States Food and Drug Administration has issued a public health announcement concerning the withdrawal of Permax (Pergolide) from the market due to a link of increased heart valve damage in its consumers. The advisory indicates two new studies showed patient's with Parkinson' Disease, who ingested pergolide, were at a higher risk of developing cardiovascular problems than those who did...

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In the latest Vioxx trial, a Madison County jury found in favor of Merck & Co. after deliberating for more than 6 hours over the course of two days. The jury members rejected Patty Schwaller widower's claim that Merck & Co. was to blame for his wife's sudden death linked to cardiovascular side effects. In siding with Merck, the jury concluded that Vioxx was not a "proximate cause" in the death...

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RotaTeq, a vaccine manufactured by Merck & Co., that received FDA approval in February of 2006, is currently being investigated for a connection to a condition called intussusception. Intussusception is a very serious and life threatening condition that causes the intestines to twist and form blockages. It is a fairly rare condition, but more than 28 cases have been reported lately in various...

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The Plaintiff's side of the case has been concluded in Madison County where the family of Patricia Schwaller has alleged that Vioxx contributed to and caused the 52-year-olds death. It was shown in the Plaintiff's case in chief that Schwaller, who died in 2003, did not have a history of heart attacks, strokes or other symptoms of congestive heart disease prior to her use of Merck & Co.'s Vioxx....

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If you currently take Ambien,Butisol Sodium, Carbrital, Dalmane, Doral, Halcion, Lunesta, Placidyl, Prosom, Restoril, Rozerem, Seconal, and/or Sonata you ought to be aware of a recent concern issued by the U.S. Food and Drug Administration relating to their use in connection with some very serious side effects. The drugs listed above are commonly prescribed to millions of consumers to address...

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An Atlantic City jury returned a plaintiff's verdict today against Merck & Co. to the tune of $47.5 million after its arthritis drug Vioxx lead to an Idaho postal worker's heart attack. $20 of the $47.5 million was awarded for compensatory damages and the remaining $27.5 million was awarded as punitive damages in order to punish Merck & Co. for their failure to warn about the cardiovascular...

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Do you or a loved one use an anemia drug? If so, you ought to be aware of a recent U.S. Food and Drug Administration warning associated with the use of prescription anemia drugs that can cause an increased risk of death or other serious side effects linked to cancer or kidney disease. The drugs, commonly sold as Procrit, Epogen and Aranesp, are designed to increase red blood cell counts and...

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The mandate of a black box warning by the U.S. Food and Drug Administration concerning many antidepressant medications over the last few years has sparked a debate among many scholars as to whether the mandate has caused an increase in teenage suicide. The warning, which informed doctors of a potential risk of increased suicidal thoughts among its users, was ordered by the FDA in 2004 on...

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The U.S. Food and Drug Administration announced last Friday that it no longer intends to publish a public list of potentially dangerous prescription drugs that was going to warn the consuming public of potential safety concerns and risks. The idea was discussed and proposed by the FDA after the withdrawal of Merck & Co.'s arthritis drug Vioxx in 2004. Instead now the FDA has decided it will only...

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The U.S. Food and Drug Administration panel has set out to review Arcoxia, Merck & Co. Inc.'s replacement pain reliever drug for Vioxx which was recalled back in 2004. In a meeting set for April 12, 2007, the panel expects to discuss the safety and effectiveness of Arcoxia which is being heavily pushed by Merck for FDA approval. Of note worthy concern, Arcoxia, like Vioxx and Bextra, is a cox-2...

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In the latest New Jersey Vioxx trial, the jurors rendered a verdict in favor of the plaintiff, Frederick "Mike" Humeston, who took Vioxx prior to his death. In this bifurcated preceding designed only to address Merck's potential liability, the New Jersey state court jury found that Merck & Company failed to warn about the dangers associated with Vioxx in causing cardiovascular risks and...

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