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Millions of Americans with moderate to severe acute pain and their health-care providers will soon have a new treatment option. Today, Johnson & Johnson Pharmaceutical Research & Development, L.L.C., (J&JPRD), announced that the U.S. Food and Drug Administration (FDA) approved tapentadol immediate-release tablets for the relief of moderate to severe acute pain in adults 18 years of age or older.
Millions of Americans with moderate to severe acute pain and their health-care providers will soon have a new treatment option.
The first melatonergic antidepressant - Valdoxan®/Thymanax® - has received a positive opinion from the European Medicines Agency's Committee for Medicinal Products for Human Use for its use in the treatment of adult patients with major depressive disorder .
(ARA) - The struggling economy can be worrisome and may make you feel blue, but how do you know if it's something more serious?
To gain approval for treating children, all a drug company has to do is submit two positive studies to the FDA to prove a medication is safe and effective for kids.
NEW YORK----Reportlinker.com announces that a new market research report related to the Pharmaceutical industry industry is available in its catalogue.
Growing your own food is better for your health.
CNS Response, Inc. (OTCBB: CNSO) reported today the results of a study presented at the U.S. Psychiatric and Mental Health Congress by Daniel Hoffman, M.D., Chief Medical Officer for CNS Response.
Decision Resources, one of the world's leading research and advisory firms focusing on pharmaceutical and healthcare issues, forecasts that the Chinese major depression drug market will triple by 2012, growing from $75 million in 2007 to $226 million in 2012.
One of Philadelphia's bellwether cases in litigation over whether the maker of the drug Paxil failed to warn about an increased risk of suicide from its drug has been dismissed following a Common Pleas Court judge's decision to grant summary judgment on statute of limitations grounds.
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