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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 Device delivery system issue? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Device delivery system issue have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.0% of all adverse event reports for GOLIMUMAB.

12
Reports of Device delivery system issue with GOLIMUMAB
0.0%
of all GOLIMUMAB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device delivery system issue From GOLIMUMAB?

Of the 12 reports, 1 (8.3%) required hospitalization.

Is Device delivery system issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 12 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 Device delivery system issue?

ALBUTEROL (9,509) SOMATROPIN (1,848) EXENATIDE (1,533) BUDESONIDE\FORMOTEROL (1,260) BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181) BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523) LEVALBUTEROL (459) MOMETASONE FUROATE\OLOPATADINE (347) ABATACEPT (342) PEGFILGRASTIM (323)

Which GOLIMUMAB Alternatives Have Lower Device delivery system issue Risk?

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

Related Pages

GOLIMUMAB Full Profile All Device delivery system issue Reports All Drugs Causing Device delivery system issue GOLIMUMAB Demographics