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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 REMICADE Cause Adverse event? 24 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Adverse event have been filed in association with REMICADE. This represents 0.8% of all adverse event reports for REMICADE.

24
Reports of Adverse event with REMICADE
0.8%
of all REMICADE reports
1
Deaths
12
Hospitalizations

How Dangerous Is Adverse event From REMICADE?

Of the 24 reports, 1 (4.2%) resulted in death, 12 (50.0%) required hospitalization.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REMICADE. However, 24 reports have been filed with the FAERS database.

What Other Side Effects Does REMICADE Cause?

Infusion related reaction (313) Crohn's disease (193) Drug ineffective (157) Dyspnoea (141) Exposure during pregnancy (96) Arthralgia (95) Nausea (85) Pain (84) Vomiting (81) Malaise (80)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which REMICADE Alternatives Have Lower Adverse event Risk?

REMICADE vs REMIFENTANIL REMICADE vs REMIMAZOLAM REMICADE vs REMODULIN REMICADE vs REPAGLINIDE REMICADE vs REPOTRECTINIB

Related Pages

REMICADE Full Profile All Adverse event Reports All Drugs Causing Adverse event REMICADE Demographics