Does METHOCARBAMOL Cause Product use issue? 90 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 90 reports of Product use issue have been filed in association with METHOCARBAMOL (Methocarbamol Tablets, USP, 500 mg). This represents 4.1% of all adverse event reports for METHOCARBAMOL.
90
Reports of Product use issue with METHOCARBAMOL
4.1%
of all METHOCARBAMOL reports
5
Deaths
80
Hospitalizations
How Dangerous Is Product use issue From METHOCARBAMOL?
Of the 90 reports, 5 (5.6%) resulted in death, 80 (88.9%) required hospitalization, and 3 (3.3%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHOCARBAMOL. However, 90 reports have been filed with the FAERS database.
What Other Side Effects Does METHOCARBAMOL Cause?
Drug ineffective (294)
Completed suicide (277)
Toxicity to various agents (166)
Drug hypersensitivity (162)
Drug dependence (130)
Drug abuse (121)
Hypertension (119)
Off label use (105)
Respiratory depression (104)
Nausea (95)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which METHOCARBAMOL Alternatives Have Lower Product use issue Risk?
METHOCARBAMOL vs METHOHEXITAL
METHOCARBAMOL vs METHOTREXATE
METHOCARBAMOL vs METHOXSALEN
METHOCARBAMOL vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA
METHOCARBAMOL vs METHYL ALCOHOL