Archive for the ‘Drug Defects’ Category

Another Counterfeit Cancer Medication Found in the U.S.

Counterfeit Altuzan Vial

The U.S. Food and Drug Administration (FDA) have issued a warning to consumers and medical professionals. FDA labs have verified that a counterfeit version of Roche’s Altuzan 400mg/16ml (bevacizumab) has been found in the U.S. Altuzan is used to treat a certain type of brain tumor as

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Glenmark Generics Issues Birth Control Recall

Glenmark Generics Norgestimate

A nationwide recall of of seven (7) lots (8 million pills) of oral contraceptives Norgestimate and Ethinyl Estradiol Tablets USP (0.18 mg/0.035 mg, 0.215 mg/0.035 mg, 0.25 mg/0.035 mg) has been issued by Glenmark Generics Inc. The recall was issued as a result of a packaging error

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FDA Sends Warning About Counterfeit Cancer Medication Avastin

Roche Avastin

The U.S. Food and Drug Administration (FDA) has issued a warning to Oncology physicians, pharmacies and patients about a counterfeit version of Avastin 400mg/16mL. The counterfeit Avastin may have been bought and administered by some U.S. medical practices. The counterfeit version is labeled and the Roche version

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Pfizer Recalls Lo/Ovral 28 Contraceptive Tablets

Pfizer Inc. has notified medical professionals and consumers that it has recalled 14 lots of Lo/Ovral-28 Tablets and 14 lots of the generic equivalent, Norgestrel and Ethinyl Estradiol Tablets, for consumers in the U.S. market. A Pfizer investigation revealed the oral contraceptive tablets found that the blister

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Off-Label Steroid Use as Epidural Linked to Serious Injury and Death

Kenalog, made by Bristol-Myers Squibb Co. and Phizer’s Depo-Medrol are steroid injections intended for use in neck and back pain patients. According to Bloomberg, both steroids are the most commonly used in an off-label manner for epidural procedures. The same Bloomberg report states that over 8 million

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European Regulators Seek Actos Bladder Cancer Warning

The European Medicines Agency (EMA) will allow Actos, to remain on the market in Europe, with more serious warnings regarding potential bladder cancer risks. Actos is Takeda Pharmaceutical’s controversial Type 2 diabetes drug.  A report from the EMA’s Committee for Medicinal Products for Human Use determined that

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Government Urges Glaxo to Mediate More Avandia Cases

In an article published yesterday, we wrote that GlaxoSmithKline agreed to pay $3 billion in order to settle several federal investigations into its drug marketing practices, including Avandia its Type 2 diabetes drug that has been linked to cardiovascular injuries. According to Bloomberg Businessweek, a U.S. District

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GlaxoSmithKline to Settle Federal Drug Marketing Invesigation

Bloomberg News has reported that GlaxoSmithKline has agreed to pay $3 billion to resolve federal investigations into the marketing of some of its drugs, including Type 2 diabetes drug Avandia. The deal with the U.S. Justice Department would account for GlaxoSmithKline’s largest legal settlement to date. The

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Another Avandia Lawsuit Filed in Illinois

Two Illinois plaintiffs have filed a lawsuit against GlaxoSmithKline alleging they should have never sold Avandia without warning consumers about the potential for serious side effects, such as heart attacks and congestive heart failure which the plaintiffs state they have suffered. The lawsuit was filed by the

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Avandia Named in Texas Lawsuit

A group of 8 plaintiffs have filed suit against against GlaxoSmithKline in Texas over alleged damage caused by Avandia. According to court filings, the plaintiffs allege that the use of Avandia caused them to suffer various heart and cardiovascular problems. The plaintiffs are seeking a full refund

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