ARMODAFINIL
Generic: ARMODAFINIL
Aurobindo Pharma LimitedManufacturer
ORALRoute
ARMODAFINILActive Substance
2018-03-06Original Approval
ARMODAFINIL is FDA application ANDA206069, sponsored by AUROBINDO PHARMA LTD. 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
FATIGUE
350 reports
2
DRUG INEFFECTIVE
306 reports
3
NAUSEA
297 reports
4
HEADACHE
253 reports
5
ANXIETY
247 reports
6
SOMNOLENCE
231 reports
7
DIZZINESS
200 reports
8
PRODUCT ADMINISTRATION INTERRUPTED
193 reports
9
DEPRESSION
190 reports
10
FALL
182 reports