BRINZOLAMIDE
Generic: BRINZOLAMIDE
Oceanside Pharmaceuticals.Manufacturer
OPHTHALMICRoute
BRINZOLAMIDEActive Substance
2021-08-18Original Approval
BRINZOLAMIDE is FDA application ANDA204884, sponsored by BAUSCH AND LOMB. 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
DIZZINESS
324 reports
2
DYSPNOEA
311 reports
3
FALL
283 reports
4
EYE PAIN
278 reports
5
DIARRHOEA
262 reports
6
ARTHRALGIA
255 reports
7
PRURITUS
250 reports
8
HEADACHE
249 reports
9
HAEMORRHAGIC STROKE
247 reports
10
MALAISE
246 reports