Does METHOCARBAMOL Cause Product administration interrupted? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product administration interrupted have been filed in association with METHOCARBAMOL (Methocarbamol Tablets, USP, 500 mg). This represents 0.3% of all adverse event reports for METHOCARBAMOL.
6
Reports of Product administration interrupted with METHOCARBAMOL
0.3%
of all METHOCARBAMOL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration interrupted From METHOCARBAMOL?
Of the 6 reports, 2 (33.3%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHOCARBAMOL. However, 6 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 administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which METHOCARBAMOL Alternatives Have Lower Product administration interrupted Risk?
METHOCARBAMOL vs METHOHEXITAL
METHOCARBAMOL vs METHOTREXATE
METHOCARBAMOL vs METHOXSALEN
METHOCARBAMOL vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA
METHOCARBAMOL vs METHYL ALCOHOL