Does METHOTREXATE Cause Device material issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device material issue have been filed in association with METHOTREXATE (Methotrexate). This represents 0.0% of all adverse event reports for METHOTREXATE.
9
Reports of Device material issue with METHOTREXATE
0.0%
of all METHOTREXATE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Device material issue From METHOTREXATE?
Of the 9 reports, 5 (55.6%) required hospitalization.
Is Device material issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHOTREXATE. However, 9 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 material issue?
COPPER (603)
SOMATROPIN (472)
CARBIDOPA\LEVODOPA (68)
ADALIMUMAB (62)
ESTRADIOL (51)
PEGFILGRASTIM (33)
ESTRADIOL\LEVONORGESTREL (24)
ABATACEPT (14)
LEVONORGESTREL (13)
BACLOFEN (11)
Which METHOTREXATE Alternatives Have Lower Device material issue Risk?
METHOTREXATE vs METHOXSALEN
METHOTREXATE vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA
METHOTREXATE vs METHYL ALCOHOL
METHOTREXATE vs METHYLCOBALAMIN
METHOTREXATE vs METHYLDOPA