IVERMECTIN
Generic: IVERMECTIN
Viona Pharmaceuticals IncManufacturer
TOPICALRoute
IVERMECTINActive Substance
2022-08-02Original Approval
IVERMECTIN is FDA application ANDA215210, sponsored by ZYDUS LIFESCIENCES. 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
OFF LABEL USE
375 reports
2
DRUG INEFFECTIVE
363 reports
3
PRODUCT USE IN UNAPPROVED INDICATION
246 reports
4
HEADACHE
156 reports
5
FATIGUE
120 reports
6
ASTHENIA
117 reports
7
NAUSEA
113 reports
8
PYREXIA
112 reports
9
STRONGYLOIDIASIS
102 reports
10
VOMITING
100 reports