GALANTAMINE
Generic: GALANTAMINE
Aurobindo Pharma LimitedManufacturer
ORALRoute
GALANTAMINE HYDROBROMIDEActive Substance
2011-03-29Original Approval
GALANTAMINE is FDA application ANDA090957, 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
FALL
812 reports
2
COGNITIVE DISORDER
664 reports
3
CONSTIPATION
651 reports
4
BALANCE DISORDER
632 reports
5
HYPOTENSION
631 reports
6
ORTHOSTATIC HYPOTENSION
625 reports
7
SEDATION
588 reports
8
DEPRESSED LEVEL OF CONSCIOUSNESS
564 reports
9
PAIN
551 reports
10
CREATININE RENAL CLEARANCE DECREASED
531 reports