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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does GABAPENTIN Cause Recalled product administered? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Recalled product administered have been filed in association with GABAPENTIN (Gabapentin). This represents 0.0% of all adverse event reports for GABAPENTIN.

6
Reports of Recalled product administered with GABAPENTIN
0.0%
of all GABAPENTIN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Recalled product administered From GABAPENTIN?

Of the 6 reports.

Is Recalled product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GABAPENTIN. However, 6 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 Recalled product administered?

RAMIPRIL (1,028) LISINOPRIL (744) PENICILLIN G BENZATHINE (500) LEVOTHYROXINE (406) HUMAN IMMUNOGLOBULIN G (382) VARENICLINE (381) VALSARTAN (267) QUINAPRIL (243) TRIAMCINOLONE ACETONIDE (222) RANITIDINE (204)

Which GABAPENTIN Alternatives Have Lower Recalled product administered Risk?

GABAPENTIN vs GABAPENTIN ENACARBIL GABAPENTIN vs GADAVIST GABAPENTIN vs GADOBENATE DIMEGLUMINE GABAPENTIN vs GADOBUTROL GABAPENTIN vs GADODIAMIDE

Related Pages

GABAPENTIN Full Profile All Recalled product administered Reports All Drugs Causing Recalled product administered GABAPENTIN Demographics