Does GOLIMUMAB Cause Product storage error? 381 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 381 reports of Product storage error have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.6% of all adverse event reports for GOLIMUMAB.
381
Reports of Product storage error with GOLIMUMAB
0.6%
of all GOLIMUMAB reports
0
Deaths
26
Hospitalizations
How Dangerous Is Product storage error From GOLIMUMAB?
Of the 381 reports, 26 (6.8%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 381 reports have been filed with the FAERS database.
What Other Side Effects Does GOLIMUMAB Cause?
Drug ineffective (17,959)
Rheumatoid arthritis (12,272)
Pain (11,443)
Fatigue (9,626)
Off label use (8,764)
Alopecia (8,394)
Rash (8,331)
Joint swelling (8,264)
Arthralgia (7,968)
Abdominal discomfort (7,902)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which GOLIMUMAB Alternatives Have Lower Product storage error Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN