St. Jude gets FDA OK for pain treatment device
AP - 6 minutes agoMedical device maker St. Jude Medical Inc. said Friday the Food and Drug Administration approved a new neurostimulation device aimed at treating pain.
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Medical device maker St. Jude Medical Inc. said Friday the Food and Drug Administration approved a new neurostimulation device aimed at treating pain.
AstraZeneca Gets FDA OK For Seroquel XR Add-on
An experimental treatment targeting hepatitis C was able to inhibit replication of the virus in the bloodstream of chimpanzees and could treat chronic infections in humans, a new study said Thursday.
A consumer group is petitioning the government to ban the weight loss pill Meridia because a recent study suggests it increases risk of heart attack, stroke and death.
Shares of Cubist Pharmaceuticals Inc. rose Thursday after an analyst upgraded the stock, saying he believes Cubist will successfully defend the patents on its antibiotic Cubicin, and expects sales will remain strong.
LONDON (SHARECAST) - The US Food and Drug Administration (FDA) has approved the use of drug giant AstraZeneca ’s bipolar disorder treatment Seroquel in conjunction with antidepressants to treat major depressive disorder (MDD).
AstraZeneca receives partial approval for depression drug from US regulators
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Abbott Laboratories Inc's weight-loss drug Meridia should be banned immediately because of heart-related risks, a consumer group said on Thursday in a petition to U.S. regulators.
The U.S. Food and Drug Administration warned Longview-based Cloud's Food Service for public health violations its inspectors found this past summer.
Targacept Inc. on Thursday struck a deal potentially worth more than $1 billion to develop a depression drugs with AstraZeneca PLC, one of the world's largest drugmakers.
A 19-year-old man wanted in connection with the death of a 22-month-old girl he was baby-sitting last weekend was arrested Wednesday night, Charlotte-Mecklenburg police said.
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ST. PAUL, Minn.----St. Jude Medical, Inc. today announced the U.S. Food and Drug Administration approval and U.S. market introduction of its new Penta™ surgical lead for neurostimulation therapy.