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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 complaint? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product use complaint have been filed in association with ICATIBANT (Icatibant). This represents 0.2% of all adverse event reports for ICATIBANT.

12
Reports of Product use complaint with ICATIBANT
0.2%
of all ICATIBANT reports
0
Deaths
6
Hospitalizations

How Dangerous Is Product use complaint From ICATIBANT?

Of the 12 reports, 6 (50.0%) required hospitalization, and 3 (25.0%) were considered life-threatening.

Is Product use complaint Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ICATIBANT. However, 12 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) Product use issue (332) Injection site pain (331) Inappropriate schedule of product administration (305) Headache (294) Malaise (262)

What Other Drugs Cause Product use complaint?

TROFINETIDE (472) ENZALUTAMIDE (336) LIFITEGRAST (326) VOXELOTOR (298) CLASCOTERONE (285) NIRMATRELVIR\RITONAVIR (248) ABALOPARATIDE (224) ESTRADIOL (208) MOLNUPIRAVIR (206) ACETAMINOPHEN (202)

Which ICATIBANT Alternatives Have Lower Product use complaint 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 complaint Reports All Drugs Causing Product use complaint ICATIBANT Demographics