FDA Duloxetine recall flags 7,100+ bottles of generic Cymbalta antidepressants
A Duloxetine recall by the FDA has flagged more than 7,100 bottles of the Cymbalta generic drug due to a cancerous chemical.
FDA recalls over 7,000 bottles of antidepressant due to possible cancerous chemical
The FDA has recalled thousands of bottles of the antidepressant duloxetine, sold under brand name Cymbalta, due to the ...
Monthly Prescribing Reference10h
Antidepressant Recalled Due to Presence of Nitrosamine Impurity
N-nitroso-duloxetine belongs to the nitrosamine class of compounds, some of which are classified as probable or possible human carcinogens.
Thousands of bottles of popular antidepressant recalled: 3 things to know
Thousands of bottles of a popular antidepressant medication are being recalled due to the presence of what the National ...
ConsumerAffairs13h
FDA recalls thousands of bottles of antidepressants over toxic chemicals
The Food and Drug Administration (FDA) has recalled over 7,000 bottles of the popular antidepressant duloxetine – sold under ...
FDA recalls more than 7,000 bottles of antidepressant duloxetine over toxic chemical
The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant duloxetine over the presence of ...
7,000 Bottles Of Antidepressants Recalled By FDA Over Possible Presence Of Cancerous Chemical
The FDA recalled more than 7,000 bottles of an antidepressant due to the presence of a carcinogenic chemical. The ...
FDA recalls over 7,000 bottles of antidepressant duloxetine
The recall was initiated due to the discovery of N-nitroso-duloxetine, a chemical impurity classified as a nitrosamine.
Becker's Hospital Review16h
FDA recalls 7,000 antidepressant bottles
The FDA's recall involves 7,107 bottles containing 500 delayed-release 20 milligram duloxetine capsules, which are prescribed to treat conditions such as anxiety, depression, nerve pain related to ...
FDA Has Recalled Thousands of Bottles of Antidepressant Duloxetine, Sold Under Brand Name Cymbalta: Here’s Why
The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the ...
People 50 and older should get pneumococcal vaccine, CDC recommends
Each year, the U.S. sees roughly 30,000 cases of invasive pneumococcal disease, which includes blood infections, brain and ...