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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 ICATIBANT Cause Product use issue? 332 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 332 reports of Product use issue have been filed in association with ICATIBANT (Icatibant). This represents 6.2% of all adverse event reports for ICATIBANT.

332
Reports of Product use issue with ICATIBANT
6.2%
of all ICATIBANT reports
3
Deaths
174
Hospitalizations

How Dangerous Is Product use issue From ICATIBANT?

Of the 332 reports, 3 (0.9%) resulted in death, 174 (52.4%) required hospitalization, and 23 (6.9%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ICATIBANT. However, 332 reports have been filed with the FAERS database.

What Other Side Effects Does ICATIBANT Cause?

Hereditary angioedema (2,221) Drug ineffective (506) Product dose omission issue (421) Weight decreased (386) Weight increased (367) Injection site pain (331) Inappropriate schedule of product administration (305) Headache (294) Malaise (262) Covid-19 (260)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which ICATIBANT Alternatives Have Lower Product use issue Risk?

ICATIBANT vs ICHTHAMMOL\ZINC ICATIBANT vs ICLUSIG ICATIBANT vs ICODEXTRIN ICATIBANT vs ICOSAPENT ICATIBANT vs ICOSAPENT ETHYL

Related Pages

ICATIBANT Full Profile All Product use issue Reports All Drugs Causing Product use issue ICATIBANT Demographics