MICONAZOLE 3
Generic: MICONAZOLE NITRATE
Rite Aid CorporationManufacturer
2004-03-30Original Approval
MICONAZOLE 3 is FDA application ANDA076357, sponsored by PERRIGO. 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
VULVOVAGINAL BURNING SENSATION
1,077 reports
2
DRUG INEFFECTIVE
785 reports
3
VULVOVAGINAL PAIN
371 reports
4
CONDITION AGGRAVATED
362 reports
5
VULVOVAGINAL PRURITUS
307 reports
6
VULVOVAGINAL DISCOMFORT
242 reports
7
VAGINAL HAEMORRHAGE
135 reports
8
VULVOVAGINAL SWELLING
125 reports
9
OFF LABEL USE
102 reports
10
HYPERSENSITIVITY
94 reports