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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 storage error? 36 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Product storage error have been filed in association with ICATIBANT (Icatibant). This represents 0.7% of all adverse event reports for ICATIBANT.

36
Reports of Product storage error with ICATIBANT
0.7%
of all ICATIBANT reports
0
Deaths
15
Hospitalizations

How Dangerous Is Product storage error From ICATIBANT?

Of the 36 reports, 15 (41.7%) required hospitalization, and 7 (19.4%) were considered life-threatening.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ICATIBANT. However, 36 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 storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Which ICATIBANT Alternatives Have Lower Product storage error 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 storage error Reports All Drugs Causing Product storage error ICATIBANT Demographics