NARATRIPTAN
Generic: NARATRIPTAN
Hikma Pharmaceuticals USA Inc.Manufacturer
ORALRoute
NARATRIPTAN HYDROCHLORIDEActive Substance
2010-07-07Original Approval
NARATRIPTAN is FDA application ANDA090381, sponsored by HIKMA. 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
DRUG INEFFECTIVE
182 reports
2
MIGRAINE
117 reports
3
NAUSEA
107 reports
4
HEADACHE
98 reports
5
FATIGUE
68 reports
6
DIZZINESS
62 reports
7
OFF LABEL USE
60 reports
8
VOMITING
59 reports
9
DIARRHOEA
58 reports
10
PAIN
51 reports