Search results for "medwatch"


 
Results 1 - 10 of about 15 for "medwatch".

FDA update

https://acpinternist.org/weekly/archives/2011/12/13/7.htm. Serious bleeding events have been reported in patients taking dabigatran (Pradaxa), according to a new FDA MedWatch alert. ... Serious bleeding events have been reported in patients taking
December 2011

Warning on an antipsychotic; generic rosuvastatin approval

Clinicians can report adverse events through MedWatch or by contacting their local FDA district office consumer complaint coordinator.
June 2016

Regulatory news

Any adverse reactions related to the recall may be reported to the FDA's MedWatch Adverse Event Reporting.
March 2011

FDA update

Any adverse events should be reported to the FDA MedWatch program and refunds for the affected products are available from.
May 2010

FDA update

Any side effects or other product problems with PPIs should be reported via the FDA's MedWatch Adverse Event Reporting program or by calling 800-332-1088.
June 2010

FDA update

Suggest a colleague as a Top Hospitalist
June 2010

Meningitis

Any suspected adverse events should be reported to the FDA's MedWatch program.
October 2012

FDA update

Health care professionals and patients are also encouraged to report any adverse events or side effects to the FDA MedWatch.
March 2010

FDA update

The FDA warned last week that proton-pump inhibitors (PPIs) may be associated with an increased risk of Clostridium difficile–associated diarrhea (CDAD).
February 2012

Warning on an antipsychotic; generic rosuvastatin approval

Clinicians can report adverse events through MedWatch or by contacting their local FDA district office consumer complaint coordinator.
July 2016

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