UPI Related News
WASHINGTON, March 5 (UPI) -- Drug counterfeiters may have added an ingredient into Chinese shipments of Baxter's blood-thinner heparin, linked to 19 deaths, a U.S agency said.
WASHINGTON, Feb. 11 (UPI) -- The U.S. Food and Drug Administration announced the Baxter Healthcare Corp. has temporarily stopped manufacturing multiple-dose vials of injectable heparin.
WASHINGTON, Feb. 6 (UPI) -- The U.S. Food and Drug Administration said it will take action against companies marketing unapproved injectable colchicine, a drug used to treat gout.
WASHINGTON, Jan. 21 (UPI) -- The U.S. Food and Drug Administration has approved a warning for the Ortho Evra Contraceptive Transdermal Patch label concerning the risk of blood clots.
WASHINGTON, Jan. 3 (UPI) -- The U.S. Food and Drug Administration said it is reviewing new data that provide further evidence of the risks of anemia drugs on tumor growth.
WASHINGTON, Dec. 12 (UPI) -- The U.S. manufacturers of drugs containing carbamazepine have agreed to warn Asian patients to get a genetic blood test before using the medication.
WASHINGTON, Nov. 2 (UPI) -- The U.S. Food and Drug Administration says consumers should stop using two unapproved drug products advertised as treatments for erectile disfunction.
WASHINGTON, Oct. 30 (UPI) -- The U.S. Food and Drug Administration has approved Tasigna (nilotinib) capsules for treatment of Philadelphia chromosome positive chronic myeloid leukemia.
WASHINGTON, Oct. 18 (UPI) -- The U.S. Food and Drug Administration announced approval Thursday of doripenem (Doribax) injections for the treatment of complex urinary tract infections.
WASHINGTON, Oct. 16 (UPI) -- The U.S. Food and Drug Administration announced approval Tuesday of raltegravir tablets for treatment of the human immunodeficiency virus.
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