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FDA Recalls Duloxetine Antidepressant for Cancer Risk
Duloxetine Recall: FDA Sets Second-Highest Risk Level for Antidepressants Containing Potential Carcinogen
Certain bottles and doses of duloxetine, a common antidepressant, have been recalled due to the presence of potentially cancer-causing chemicals. The recall was initiated on Nov. 19 by manufacturer Rising Pharma,
Antidepressant Recall Update As FDA Sets Risk Level
233,003 bottles of duloxetine have been recalled due to potentially containing high levels of cancer-causing impurities.
FDA Recalls Duloxetine Antidepressant for Cancer Risk: What to Know
Over 8 million U.S. adults take antidepressants to treat mild to moderate depression, anxiety and, in some cases, chronic pain. A recent Food and Drug Administration (FDA) recall of a commonly prescribed antidepressant,
Medscape
1mon
Duloxetine in the Treatment of Major Depressive Disorder: An Open-Label Study
Study drug consisted of 2 capsules (
30 mg
of
duloxetine
in each
capsule
) taken once-daily. If necessary due to tolerability, the dose could be reduced to 1
capsule
(
duloxetine
30 mg
/d) at ...
1mon
on MSN
FDA recalls over 7,000 bottles of antidepressant duloxetine
Earlier this week, the U.S. Food and Drug Administration announced a significant recall of over 7,100 bottles of
duloxetine
...
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