ATOMOXETINE HYDROCHLORIDE
Generic: ATOMOXETINE HYDROCHLORIDE
Advagen Pharma Ltd.Manufacturer
ORALRoute
ATOMOXETINE HYDROCHLORIDEActive Substance
2026-03-20Original Approval
ATOMOXETINE HYDROCHLORIDE is FDA application NDA220320, sponsored by MAP77. 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
OFF LABEL USE
743 reports
2
DRUG INEFFECTIVE
640 reports
3
PAIN
589 reports
4
EPILEPSY
580 reports
5
CONFUSIONAL STATE
575 reports
6
PSORIATIC ARTHROPATHY
564 reports
7
HYPOAESTHESIA
560 reports
8
MATERNAL EXPOSURE DURING PREGNANCY
558 reports
9
RHEUMATOID ARTHRITIS
556 reports
10
ABDOMINAL PAIN UPPER
554 reports