GLYBURIDE
Generic: GLYBURIDE
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.Manufacturer
ORALRoute
GLYBURIDEActive Substance
2011-02-28Original Approval
GLYBURIDE is FDA application ANDA090937, sponsored by HERITAGE. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
BLOOD GLUCOSE INCREASED
3,059 reports
2
NAUSEA
2,049 reports
3
WEIGHT DECREASED
1,545 reports
4
DRUG INEFFECTIVE
1,439 reports
5
DIARRHOEA
1,317 reports
6
DIZZINESS
1,219 reports
7
HYPOGLYCAEMIA
1,216 reports
8
BLOOD GLUCOSE DECREASED
1,169 reports
9
FATIGUE
1,156 reports
10
DYSPNOEA
1,110 reports