Does ICATIBANT Cause Intentional product use issue? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Intentional product use issue have been filed in association with ICATIBANT (Icatibant). This represents 0.5% of all adverse event reports for ICATIBANT.
27
Reports of Intentional product use issue with ICATIBANT
0.5%
of all ICATIBANT reports
2
Deaths
15
Hospitalizations
How Dangerous Is Intentional product use issue From ICATIBANT?
Of the 27 reports, 2 (7.4%) resulted in death, 15 (55.6%) required hospitalization, and 2 (7.4%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ICATIBANT. However, 27 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ICATIBANT Alternatives Have Lower Intentional product use issue Risk?
ICATIBANT vs ICHTHAMMOL\ZINC
ICATIBANT vs ICLUSIG
ICATIBANT vs ICODEXTRIN
ICATIBANT vs ICOSAPENT
ICATIBANT vs ICOSAPENT ETHYL