Does METHOCARBAMOL Cause Product prescribing error? 87 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 87 reports of Product prescribing error have been filed in association with METHOCARBAMOL (Methocarbamol Tablets, USP, 500 mg). This represents 4.0% of all adverse event reports for METHOCARBAMOL.
87
Reports of Product prescribing error with METHOCARBAMOL
4.0%
of all METHOCARBAMOL reports
5
Deaths
76
Hospitalizations
How Dangerous Is Product prescribing error From METHOCARBAMOL?
Of the 87 reports, 5 (5.7%) resulted in death, 76 (87.4%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHOCARBAMOL. However, 87 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which METHOCARBAMOL Alternatives Have Lower Product prescribing error Risk?
METHOCARBAMOL vs METHOHEXITAL
METHOCARBAMOL vs METHOTREXATE
METHOCARBAMOL vs METHOXSALEN
METHOCARBAMOL vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA
METHOCARBAMOL vs METHYL ALCOHOL