Does ICATIBANT Cause Product prescribing error? 75 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 75 reports of Product prescribing error have been filed in association with ICATIBANT (Icatibant). This represents 1.4% of all adverse event reports for ICATIBANT.
75
Reports of Product prescribing error with ICATIBANT
1.4%
of all ICATIBANT reports
4
Deaths
27
Hospitalizations
How Dangerous Is Product prescribing error From ICATIBANT?
Of the 75 reports, 4 (5.3%) resulted in death, 27 (36.0%) required hospitalization, and 14 (18.7%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ICATIBANT. However, 75 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which ICATIBANT Alternatives Have Lower Product prescribing error Risk?
ICATIBANT vs ICHTHAMMOL\ZINC
ICATIBANT vs ICLUSIG
ICATIBANT vs ICODEXTRIN
ICATIBANT vs ICOSAPENT
ICATIBANT vs ICOSAPENT ETHYL