Does GABAPENTIN Cause Product use in unapproved indication? 4,919 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,919 reports of Product use in unapproved indication have been filed in association with GABAPENTIN (Gabapentin). This represents 6.6% of all adverse event reports for GABAPENTIN.
4,919
Reports of Product use in unapproved indication with GABAPENTIN
6.6%
of all GABAPENTIN reports
206
Deaths
965
Hospitalizations
How Dangerous Is Product use in unapproved indication From GABAPENTIN?
Of the 4,919 reports, 206 (4.2%) resulted in death, 965 (19.6%) required hospitalization, and 210 (4.3%) 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 GABAPENTIN. However, 4,919 reports have been filed with the FAERS database.
What Other Side Effects Does GABAPENTIN Cause?
Drug ineffective (10,914)
Drug hypersensitivity (6,833)
Off label use (6,729)
Drug ineffective for unapproved indication (5,231)
Toxicity to various agents (4,839)
Completed suicide (4,111)
Dizziness (4,107)
Somnolence (3,798)
Fatigue (3,791)
Pain (3,656)
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 GABAPENTIN Alternatives Have Lower Product use in unapproved indication Risk?
GABAPENTIN vs GABAPENTIN ENACARBIL
GABAPENTIN vs GADAVIST
GABAPENTIN vs GADOBENATE DIMEGLUMINE
GABAPENTIN vs GADOBUTROL
GABAPENTIN vs GADODIAMIDE