CEVIMELINE HYDROCHLORIDE
Generic: CEVIMELINE HYDROCHLORIDE
Hikma Pharmaceuticals USA Inc.Manufacturer
ORALRoute
CEVIMELINE HYDROCHLORIDEActive Substance
2013-07-08Original Approval
CEVIMELINE HYDROCHLORIDE is FDA application ANDA091591, 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
43 reports
2
FATIGUE
37 reports
3
HEADACHE
36 reports
4
NAUSEA
36 reports
5
PRODUCT DOSE OMISSION ISSUE
32 reports
6
EYE PAIN
30 reports
7
DIARRHOEA
28 reports
8
ARTHRALGIA
25 reports
9
MALAISE
25 reports
10
PAIN
25 reports