Does METHOTREXATE Cause Product dose omission issue? 1,170 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,170 reports of Product dose omission issue have been filed in association with METHOTREXATE (Methotrexate). This represents 0.5% of all adverse event reports for METHOTREXATE.
1,170
Reports of Product dose omission issue with METHOTREXATE
0.5%
of all METHOTREXATE reports
44
Deaths
337
Hospitalizations
How Dangerous Is Product dose omission issue From METHOTREXATE?
Of the 1,170 reports, 44 (3.8%) resulted in death, 337 (28.8%) required hospitalization, and 38 (3.2%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHOTREXATE. However, 1,170 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which METHOTREXATE Alternatives Have Lower Product dose omission issue Risk?
METHOTREXATE vs METHOXSALEN
METHOTREXATE vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA
METHOTREXATE vs METHYL ALCOHOL
METHOTREXATE vs METHYLCOBALAMIN
METHOTREXATE vs METHYLDOPA