Cymbalta recall

PLEASE NOTE WE ARE NO LONGER TAKING CYMBALTA CASES. Individuals Other drugs are not subject to a recall but may cause injuries nonetheless.

Cymbalta in the first cases slated to be heard by juries BMW Took Two Years to Find Extent of Defect Behind Recall. Add more

Teva Pharmaceutical Industries voluntarily recalled 19 lots of duloxetine, a generic version of Eli Lilly's antidepressant Cymbalta, after a customer complaint. The recall affected more than 1 million bottles and was not related to the drug's safety or efficacy.

The FDA approved Cymbalta (duloxetine hydrochloride) to treat chronic recall of 0.84, specificity of 0.82 and AUROC of 0.86 for

HealthProfessionals to access drug-related databases, information on drug recalls and alerts, current information 4 Cymbalta (duloxetine) prescribing

A recall of Fentanyl transdermal systems after laboratory testing A new indication for duloxetine hydrochloride (Cymbalta) to treat chronic

The FDA approved Cymbalta (duloxetine hydrochloride) to treat chronic recall of 0.84, specificity of 0.82 and AUROC of 0.86 for

The drug Duloxetine (also known as Cymbalta) generally used to treat depression, anxiety, and chronic pain has undergone a Class 3 recall by

DePuy ASR Hip Recall Lawsuits Hip Lawsuit, Replacement, Recall, Information Cymbalta (duloxetine) is a serotonin-norepinephrine reuptake inhibitor