A New Jersey pharmaceutical company is recalling more than 230,000 bottles of duloxetine antidepressants after detecting a ...
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An SNRI (serotonin and norepinephrine reuptake inhibitor) is one of two major classes of medications used to treat clinical ...
In three separate reports, the FDA said that various doses of duloxetine delayed-release capsules were recalled due to the ...
The bottles were distributed nationwide, including in Wisconsin, and received the FDA's second-most severe risk ...
233,003 bottles of duloxetine have been recalled due to potentially containing high levels of cancer-causing impurities.
More than 233,000 bottles of an antidepressant have been recalled by the FDA due to the presence of duloxetine posing the risk of cancer.
The Food and Drug Administration has recalled Duloxetine, a commonly prescribed antidepressant, due to fears it could contain ...
Certain bottles and doses of duloxetine, a common antidepressant, have been recalled due to the presence of potentially ...
Duloxetine is an antidepressant, with a specific batch having been recalled due to the presence of potentially cancer-causing ...
Rising Pharmaceuticals has voluntarily recalled over 233,000 bottles of Duloxetine in the US due to potential contamination ...
Over 8 million U.S. adults take antidepressants to treat mild to moderate depression, anxiety and, in some cases, chronic ...