Does ICATIBANT Cause Expired product administered? 84 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 84 reports of Expired product administered have been filed in association with ICATIBANT (Icatibant). This represents 1.6% of all adverse event reports for ICATIBANT.
84
Reports of Expired product administered with ICATIBANT
1.6%
of all ICATIBANT reports
2
Deaths
28
Hospitalizations
How Dangerous Is Expired product administered From ICATIBANT?
Of the 84 reports, 2 (2.4%) resulted in death, 28 (33.3%) required hospitalization, and 4 (4.8%) were considered life-threatening.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ICATIBANT. However, 84 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which ICATIBANT Alternatives Have Lower Expired product administered Risk?
ICATIBANT vs ICHTHAMMOL\ZINC
ICATIBANT vs ICLUSIG
ICATIBANT vs ICODEXTRIN
ICATIBANT vs ICOSAPENT
ICATIBANT vs ICOSAPENT ETHYL