LATANOPROST
Generic: LATANOPROST
Sandoz IncManufacturer
OPHTHALMICRoute
LATANOPROSTActive Substance
2011-03-22Original Approval
LATANOPROST is FDA application ANDA091449, sponsored by SANDOZ. 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
TREATMENT FAILURE
5,800 reports
2
DRUG INEFFECTIVE
2,212 reports
3
FATIGUE
1,702 reports
4
EYE IRRITATION
1,293 reports
5
OFF LABEL USE
1,197 reports
6
HEADACHE
1,175 reports
7
DIARRHOEA
1,172 reports
8
DIZZINESS
1,047 reports
9
NAUSEA
1,019 reports
10
DYSPNOEA
1,015 reports