Does GALANTAMINE Cause Product use in unapproved indication? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Product use in unapproved indication have been filed in association with GALANTAMINE. This represents 3.3% of all adverse event reports for GALANTAMINE.
52
Reports of Product use in unapproved indication with GALANTAMINE
3.3%
of all GALANTAMINE reports
3
Deaths
35
Hospitalizations
How Dangerous Is Product use in unapproved indication From GALANTAMINE?
Of the 52 reports, 3 (5.8%) resulted in death, 35 (67.3%) required hospitalization, and 32 (61.5%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GALANTAMINE. However, 52 reports have been filed with the FAERS database.
What Other Side Effects Does GALANTAMINE Cause?
Fall (353)
Cognitive disorder (272)
Balance disorder (259)
Orthostatic hypotension (256)
Constipation (255)
Hypotension (255)
Sedation (249)
Depressed level of consciousness (240)
Pain (230)
Toxicity to various agents (226)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which GALANTAMINE Alternatives Have Lower Product use in unapproved indication Risk?
GALANTAMINE vs GALANTAMINE HYDROBROMIDE
GALANTAMINE vs GALCANEZUMAB
GALANTAMINE vs GALCANEZUMAB-GNLM
GALANTAMINE vs GALLIUM GA-OZETOTIDE
GALANTAMINE vs GALSULFASE