Does GABAPENTIN Cause Intentional product use issue? 580 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 580 reports of Intentional product use issue have been filed in association with GABAPENTIN (Gabapentin). This represents 0.8% of all adverse event reports for GABAPENTIN.
580
Reports of Intentional product use issue with GABAPENTIN
0.8%
of all GABAPENTIN reports
48
Deaths
138
Hospitalizations
How Dangerous Is Intentional product use issue From GABAPENTIN?
Of the 580 reports, 48 (8.3%) resulted in death, 138 (23.8%) required hospitalization, and 32 (5.5%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GABAPENTIN. However, 580 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)
Product use in unapproved indication (4,919)
Toxicity to various agents (4,839)
Completed suicide (4,111)
Dizziness (4,107)
Somnolence (3,798)
Fatigue (3,791)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which GABAPENTIN Alternatives Have Lower Intentional product use issue Risk?
GABAPENTIN vs GABAPENTIN ENACARBIL
GABAPENTIN vs GADAVIST
GABAPENTIN vs GADOBENATE DIMEGLUMINE
GABAPENTIN vs GADOBUTROL
GABAPENTIN vs GADODIAMIDE