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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does METHOTREXATE Cause Device defective? 68 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Device defective have been filed in association with METHOTREXATE (Methotrexate). This represents 0.0% of all adverse event reports for METHOTREXATE.

68
Reports of Device defective with METHOTREXATE
0.0%
of all METHOTREXATE reports
0
Deaths
14
Hospitalizations

How Dangerous Is Device defective From METHOTREXATE?

Of the 68 reports, 14 (20.6%) required hospitalization, and 12 (17.6%) were considered life-threatening.

Is Device defective Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for METHOTREXATE. However, 68 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 Device defective?

SOMATROPIN (1,719) USTEKINUMAB (1,071) SECUKINUMAB (666) GUSELKUMAB (574) GOLIMUMAB (539) ABATACEPT (458) ALBUTEROL (445) TOCILIZUMAB (400) INSULIN GLARGINE (397) EXENATIDE (387)

Which METHOTREXATE Alternatives Have Lower Device defective Risk?

METHOTREXATE vs METHOXSALEN METHOTREXATE vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA METHOTREXATE vs METHYL ALCOHOL METHOTREXATE vs METHYLCOBALAMIN METHOTREXATE vs METHYLDOPA

Related Pages

METHOTREXATE Full Profile All Device defective Reports All Drugs Causing Device defective METHOTREXATE Demographics