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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 container issue? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product container issue have been filed in association with ICATIBANT (Icatibant). This represents 0.2% of all adverse event reports for ICATIBANT.

10
Reports of Product container issue with ICATIBANT
0.2%
of all ICATIBANT reports
0
Deaths
3
Hospitalizations

How Dangerous Is Product container issue From ICATIBANT?

Of the 10 reports, 3 (30.0%) required hospitalization.

Is Product container issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ICATIBANT. However, 10 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 container issue?

CYCLOSPORINE (910) MINOXIDIL (556) MOMETASONE FUROATE (450) FORMOTEROL\MOMETASONE FUROATE (375) LIFITEGRAST (244) ALBUTEROL (192) LATANOPROST (158) CARBOXYMETHYLCELLULOSE\GLYCERIN (123) BRIMONIDINE (121) ACETAMINOPHEN (118)

Which ICATIBANT Alternatives Have Lower Product container 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 container issue Reports All Drugs Causing Product container issue ICATIBANT Demographics