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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 Drug dose omission? 2,652 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 2,652 reports of Drug dose omission have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 3.8% of all adverse event reports for GOLIMUMAB.

2,652
Reports of Drug dose omission with GOLIMUMAB
3.8%
of all GOLIMUMAB reports
1
Deaths
91
Hospitalizations

How Dangerous Is Drug dose omission From GOLIMUMAB?

Of the 2,652 reports, 1 (0.0%) resulted in death, 91 (3.4%) required hospitalization, and 3 (0.1%) were considered life-threatening.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 2,652 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 Drug dose omission?

ETANERCEPT (10,871) CINACALCET (8,683) EVOLOCUMAB (4,914) ADALIMUMAB (3,993) INSULIN LISPRO (3,063) TERIPARATIDE (2,616) APREMILAST (2,466) ALBUTEROL (2,309) FLUTICASONE\SALMETEROL (2,153) PEGFILGRASTIM (2,089)

Which GOLIMUMAB Alternatives Have Lower Drug 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 Drug dose omission Reports All Drugs Causing Drug dose omission GOLIMUMAB Demographics