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Top Breaking News
FDA Slaps Valeant (VRX) With A Warning Letter     10/1/2014
FDA Says Novartis AG (NVS), Roche (RHHBY)'s Asthma Drug Xolair Raises Risk Of Heart, Brain Problems     9/29/2014
Biomedic Acetaminophen With Codeine: Recall Due To Missing Child-Resistant Packaging     9/29/2014
FDA Slaps Pacira Pharmaceuticals, Inc. (PCRX) With Warning Letter     9/26/2014
Pfizer (PFE) Wants Black Box Warning From Chantix     9/25/2014
GlaxoSmithKline (GSK) Deals With Fallout From Polio Virus Spill     9/23/2014
FDA Chides Cipher Pharmaceuticals (DND.TO) Over Cholesterol Drug Ad's Superiority Claims     9/22/2014
Health Canada Requests Quarantine Of Ipca Laboratories' Products Following Falsification And Manipulation Of Data Issues     9/19/2014
Baxter International, Inc. (BAX) Recalls One Lot Of Potassium Chloride Injection     9/18/2014
Human Hair Discovered In Heparin Vial Prompts Hospira, Inc. Recalls     9/17/2014
Hundreds Of Girls Struck With Mystery Illness; Possibly Linked To Merck & Co. (MRK)'s Gardasil     8/29/2014
FDA Chastises Alexion Pharmaceuticals Inc. (ALXN) For Production Problems Again     8/28/2014
Teva Pharmaceutical Industries Limited (TEVA) Recalls Parkinson's Disease Medication As It May Be "Super Potent"     8/28/2014
FDA Finds Falsified Data, Serious Mold, And Decaying Frogs At Amanta (Formerly Known As Marck Biosciences)     8/21/2014
Dr. Reddy's Laboratories, Inc. (RDY)'s Breached Packaging Rules: U.S. Regulator     8/21/2014

Featured Stories
Popular Acne Products Can Be Dangerous, FDA Reveals     6/26/2014
FDA Orders Testosterone Supplement Makers To Include Blood Clot Warnings     6/23/2014
Popular Weight-Loss Supplement Linked to Hepatitis and Liver Failure, USPLabs Reveals     10/11/2013
What Did Mylan Inc. (MYL) Get for $1.6 Billion? A Vaccine Maker With a Troubled Factory     9/25/2013
FDA: 5-Hour Energy Drink Linked to Deaths     11/16/2012
Diabetics in Danger After Drug Sparks Health Alert, Irish Medicines Board Reveals     3/16/2012
Neti Pots Linked to Brain-Eating Amoeba Deaths     12/20/2011
FDA, Federal Trade Commission Act to Remove "Homeopathic" HCG Weight Loss Products from the Market     12/6/2011
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
AstraZeneca PLC (AZN)'s $6 Billion Stomach Ache: Nexium Causes Bone Fractures     4/22/2011
FDA Says No Fracture Warning Needed for OTC Ulcer Drugs     3/24/2011
US FDA Pulls 500 Unauthorized Prescription Drugs     3/4/2011
FDA Orders New Cautions on Antipsychotic Drugs     2/23/2011
Warning on Danger of Splitting Tablets, Ghent University Study     1/6/2011
Recalled Drugs Tied to Heart Risk Spurs Call for FDA Review     9/29/2010
Mylan Pharmaceuticals, Inc. (MYL) Recalls Nitroglycerin Spray Due To Defective Pump     9/22/2014
Aegerion Pharmaceuticals, Inc. (AEGR) Announces Resolution Of Warning Letter For JUXTAPID® (Lomitapide) Capsules     8/27/2014
Cubist Pharmaceuticals, Inc. (CBST) Issues Voluntary Nationwide Recall Of Nine Lots Of CUBICIN (Daptomycin For Injection) 500 Mg In 10 Ml Single Use Vials Following Complaints Of Foreign Particulate Matter In Reconstituted Vials     8/11/2014
Cubist Pharmaceuticals, Inc. (CBST) Issues Voluntary Nationwide Recall Of One Lot Of CUBICIN (Daptomycin For Injection) 500 Mg In 10 Ml Single Use Vials Due To Presence Of Particulate Matter     4/18/2014
Trouble for Bliss GVS Pharma Drug in Ghana     10/8/2013
Tobinco to Compensate Customers on the Recall of Gsunate Plus Suppository by FDA     9/17/2013
Fresenius Kabi USA Issues Voluntary Nationwide Recall of Benztropine Mesylate Injection, USP 2 mg/2 mL (1 mg/mL), in 2 mL Single Dose Vials     7/1/2013
Sagent Pharmaceuticals, Inc. Expands a Nationwide Voluntary Recall to All Lots of Vecuronium Bromide for Injection, 10mg Single Use Vials Manufactured by Mustafa Nevzat (MN Pharmaceuticals)     6/13/2013
Novo Nordisk A/S (NVO): Previously Announced FDA Warning Letter Published     2/5/2013
FDA Recalls Hospira, Inc. (HSP)'s Lactated Ringer's and 5% Dextrose Injection, 1000 Ml, Flexible Containers     10/9/2012
Bioniche Life Sciences Inc. (BNC) Discovers a Counterfeit Equine Product     9/24/2012
Bedford Laboratories Broadens Voluntary Recall of Leucovorin Calcium Injection USP     9/18/2012
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
Sun Pharmaceutical Industries Ltd Issues Nationwide Voluntary Recall of One Lot of Nimodipine Capsules Due to Crystallization of the Fill Material     9/4/2012
Bedford Laboratories Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram Per Vial     2/16/2012

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