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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 GOLIMUMAB Cause Product dose omission? 732 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 732 reports of Product dose omission have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 1.1% of all adverse event reports for GOLIMUMAB.

732
Reports of Product dose omission with GOLIMUMAB
1.1%
of all GOLIMUMAB reports
4
Deaths
58
Hospitalizations

How Dangerous Is Product dose omission From GOLIMUMAB?

Of the 732 reports, 4 (0.5%) resulted in death, 58 (7.9%) required hospitalization.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 732 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 dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which GOLIMUMAB Alternatives Have Lower Product dose omission Risk?

GOLIMUMAB vs GOLODIRSEN GOLIMUMAB vs GONADORELIN GOLIMUMAB vs GONADOTROPHIN, CHORIONIC GOLIMUMAB vs GOSERELIN GOLIMUMAB vs GRAMICIDIN

Related Pages

GOLIMUMAB Full Profile All Product dose omission Reports All Drugs Causing Product dose omission GOLIMUMAB Demographics