ZOLMITRIPTAN
Generic: ZOLMITRIPTAN
Glenmark Pharmaceuticals Inc.Manufacturer
ORALRoute
ZOLMITRIPTANActive Substance
2013-05-14Original Approval
ZOLMITRIPTAN is FDA application ANDA201779, sponsored by GLENMARK PHARMS LTD. 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
HEADACHE
438 reports
2
OFF LABEL USE
353 reports
3
DRUG INEFFECTIVE
327 reports
4
DRUG INTOLERANCE
285 reports
5
NAUSEA
263 reports
6
MIGRAINE
225 reports
7
HYPERSENSITIVITY
218 reports
8
ANGIOEDEMA
204 reports
9
SWELLING FACE
200 reports
10
SWOLLEN TONGUE
198 reports