FDA: 5-Hour Energy Drink Linked to Deaths
11/16/2012
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Diabetics in Danger After Drug Sparks Health Alert, Irish Medicines Board Reveals
3/16/2012
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Neti Pots Linked to Brain-Eating Amoeba Deaths
12/20/2011
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FDA, Federal Trade Commission Act to Remove "Homeopathic" HCG Weight Loss Products from the Market
12/6/2011
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GlaxoSmithKline (GSK)'s Avandia - When a Drug is on The Market, But Not Really; Drug Officially Gone From US Pharmacies in November
5/19/2011
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AstraZeneca PLC (AZN)'s $6 Billion Stomach Ache: Nexium Causes Bone Fractures
4/22/2011
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FDA Says No Fracture Warning Needed for OTC Ulcer Drugs
3/24/2011
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US FDA Pulls 500 Unauthorized Prescription Drugs
3/4/2011
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FDA Orders New Cautions on Antipsychotic Drugs
2/23/2011
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Warning on Danger of Splitting Tablets, Ghent University Study
1/6/2011
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Recalled Drugs Tied to Heart Risk Spurs Call for FDA Review
9/29/2010
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Traces of CA Genetic Edge Technologies Drug Prompts Muscle Builder Recall
9/20/2010
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'Tiger Balm' Gives FDA Officials Headaches
8/16/2010
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Novo Nordisk A/S (NVO)'s Decision To Pull Mixtard 30 Insulin Drug Could Add £9 Million To NHS Drugs Bill In England Alone
8/4/2010
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New Obesity Pills Try To Shed Past Problems, VIVUS, Inc. (VVUS), Arena Pharmaceuticals, Inc. (ARNA), and Orexigen Therapeutics, Inc. (OREX) Trying to Succeed Where Earlier Efforts Flopped
7/9/2010
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Novo Nordisk A/S (NVO): Previously Announced FDA Warning Letter Published
2/5/2013
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FDA Recalls Hospira, Inc. (HSP)'s Lactated Ringer's and 5% Dextrose Injection, 1000 Ml, Flexible Containers
10/9/2012
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Bioniche Life Sciences Inc. (BNC) Discovers a Counterfeit Equine Product
9/24/2012
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Bedford Laboratories Broadens Voluntary Recall of Leucovorin Calcium Injection USP
9/18/2012
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Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall for One Lot of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg Due to the Potential for Oversized Tablets
9/11/2012
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Sun Pharmaceutical Industries Ltd Issues Nationwide Voluntary Recall of One Lot of Nimodipine Capsules Due to Crystallization of the Fill Material
9/4/2012
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Bedford Laboratories Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram Per Vial
2/16/2012
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Bedford Laboratories Issues a Voluntary Nationwide Patient Level Recall of Acetylcysteine Solution, USP, Lot 1877093
2/2/2012
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Bedford Laboratories Issues Guidance on 2011 Voluntary Recall of Polymyxin B for Injection USP and Vecuronium Bromide for Injection Related to Glass Particulates
1/11/2012
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FDA: U.S. Marshals Seize Products Containing Banned Ephedrine for Dietary Supplements
12/7/2011
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FDA: U.S. Marshals Seize Dietary Supplements, Drugs Manufactured by Syntec Inc.
12/2/2011
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FDA Updates Boxed Warning for TNF-alpha Inhibitors
9/8/2011
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American Regent, Inc. Initiates Voluntary Nationwide Recall of Calcium Gluconate Injection, USP, 10%, 100 mL Pharmacy Bulk Package Due to Particulates
7/19/2011
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Qualitest Pharmaceuticals Issues Voluntary, Nationwide Retail Level Recall of Four Lots of Butalbital, Acetaminophen, and Caffeine Tablets, USP 50mg/325mg/40mg and Four Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5MG/500MG
6/27/2011
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FDA Warns Against Repackaging Pradaxa
3/31/2011
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