DESONIDE
Generic: DESONIDE
Sun Pharmaceutical IndustriesManufacturer
TOPICALRoute
DESONIDEActive Substance
2014-10-31Original Approval
DESONIDE is FDA application ANDA202161, sponsored by TARO. 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
1,194 reports
2
MACULAR DEGENERATION
787 reports
3
OFF LABEL USE
420 reports
4
PAIN
391 reports
5
NAUSEA
375 reports
6
PRURITUS
343 reports
7
RASH
327 reports
8
HEADACHE
320 reports
9
ERYTHEMA
314 reports
10
PYREXIA
306 reports