Does METHOTREXATE Cause Product use in unapproved indication? 8,930 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8,930 reports of Product use in unapproved indication have been filed in association with METHOTREXATE (Methotrexate). This represents 3.5% of all adverse event reports for METHOTREXATE.
8,930
Reports of Product use in unapproved indication with METHOTREXATE
3.5%
of all METHOTREXATE reports
2,002
Deaths
2,876
Hospitalizations
How Dangerous Is Product use in unapproved indication From METHOTREXATE?
Of the 8,930 reports, 2,002 (22.4%) resulted in death, 2,876 (32.2%) required hospitalization, and 1,727 (19.3%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHOTREXATE. However, 8,930 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 use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
CYCLOSPORINE (5,019)
Which METHOTREXATE Alternatives Have Lower Product use in unapproved indication Risk?
METHOTREXATE vs METHOXSALEN
METHOTREXATE vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA
METHOTREXATE vs METHYL ALCOHOL
METHOTREXATE vs METHYLCOBALAMIN
METHOTREXATE vs METHYLDOPA