Does METHOTREXATE Cause Product preparation error? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Product preparation error have been filed in association with METHOTREXATE (Methotrexate). This represents 0.0% of all adverse event reports for METHOTREXATE.
21
Reports of Product preparation error with METHOTREXATE
0.0%
of all METHOTREXATE reports
0
Deaths
8
Hospitalizations
How Dangerous Is Product preparation error From METHOTREXATE?
Of the 21 reports, 8 (38.1%) required hospitalization, and 2 (9.5%) were considered life-threatening.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHOTREXATE. However, 21 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which METHOTREXATE Alternatives Have Lower Product preparation error Risk?
METHOTREXATE vs METHOXSALEN
METHOTREXATE vs METHOXY POLYETHYLENE GLYCOL-EPOETIN BETA
METHOTREXATE vs METHYL ALCOHOL
METHOTREXATE vs METHYLCOBALAMIN
METHOTREXATE vs METHYLDOPA