Does ICATIBANT Cause Condition aggravated? 135 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 135 reports of Condition aggravated have been filed in association with ICATIBANT (Icatibant). This represents 2.5% of all adverse event reports for ICATIBANT.
135
Reports of Condition aggravated with ICATIBANT
2.5%
of all ICATIBANT reports
5
Deaths
64
Hospitalizations
How Dangerous Is Condition aggravated From ICATIBANT?
Of the 135 reports, 5 (3.7%) resulted in death, 64 (47.4%) required hospitalization, and 6 (4.4%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ICATIBANT. However, 135 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ICATIBANT Alternatives Have Lower Condition aggravated Risk?
ICATIBANT vs ICHTHAMMOL\ZINC
ICATIBANT vs ICLUSIG
ICATIBANT vs ICODEXTRIN
ICATIBANT vs ICOSAPENT
ICATIBANT vs ICOSAPENT ETHYL