Does METHOTREXATE Cause Product prescribing error? 434 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 434 reports of Product prescribing error have been filed in association with METHOTREXATE (Methotrexate). This represents 0.2% of all adverse event reports for METHOTREXATE.
434
Reports of Product prescribing error with METHOTREXATE
0.2%
of all METHOTREXATE reports
58
Deaths
203
Hospitalizations
How Dangerous Is Product prescribing error From METHOTREXATE?
Of the 434 reports, 58 (13.4%) resulted in death, 203 (46.8%) required hospitalization, and 38 (8.8%) 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 METHOTREXATE. However, 434 reports have been filed with the FAERS database.
What Other Side Effects Does METHOTREXATE Cause?
Drug ineffective (70,142)
Rheumatoid arthritis (29,254)
Off label use (24,020)
Pain (23,773)
Drug intolerance (22,555)
Arthralgia (21,831)
Fatigue (19,885)
Nausea (18,715)
Joint swelling (17,657)
Drug hypersensitivity (16,677)
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)
TORSEMIDE (352)
METOPROLOL (325)
RAMIPRIL (322)
Which METHOTREXATE Alternatives Have Lower Product prescribing error Risk?
METHOTREXATE vs METHOXSALEN
METHOTREXATE vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA
METHOTREXATE vs METHYL ALCOHOL
METHOTREXATE vs METHYLCOBALAMIN
METHOTREXATE vs METHYLDOPA