Does GABAPENTIN Cause Product dose omission? 139 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 139 reports of Product dose omission have been filed in association with GABAPENTIN (Gabapentin). This represents 0.2% of all adverse event reports for GABAPENTIN.
139
Reports of Product dose omission with GABAPENTIN
0.2%
of all GABAPENTIN reports
1
Deaths
36
Hospitalizations
How Dangerous Is Product dose omission From GABAPENTIN?
Of the 139 reports, 1 (0.7%) resulted in death, 36 (25.9%) required hospitalization, and 3 (2.2%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GABAPENTIN. However, 139 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which GABAPENTIN Alternatives Have Lower Product dose omission Risk?
GABAPENTIN vs GABAPENTIN ENACARBIL
GABAPENTIN vs GADAVIST
GABAPENTIN vs GADOBENATE DIMEGLUMINE
GABAPENTIN vs GADOBUTROL
GABAPENTIN vs GADODIAMIDE