Does ECALLANTIDE Cause Product use issue? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Product use issue have been filed in association with ECALLANTIDE (Kalbitor). This represents 2.9% of all adverse event reports for ECALLANTIDE.
35
Reports of Product use issue with ECALLANTIDE
2.9%
of all ECALLANTIDE reports
0
Deaths
23
Hospitalizations
How Dangerous Is Product use issue From ECALLANTIDE?
Of the 35 reports, 23 (65.7%) required hospitalization, and 2 (5.7%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECALLANTIDE. However, 35 reports have been filed with the FAERS database.
What Other Side Effects Does ECALLANTIDE Cause?
Hereditary angioedema (519)
Off label use (139)
Drug ineffective (89)
Malaise (60)
Product dose omission issue (57)
Headache (54)
Weight decreased (52)
Pain (50)
Weight increased (47)
Hypersensitivity (38)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ECALLANTIDE Alternatives Have Lower Product use issue Risk?
ECALLANTIDE vs ECONAZOLE
ECALLANTIDE vs ECULIZUMAB
ECALLANTIDE vs EDARAVONE
ECALLANTIDE vs EDETATE
ECALLANTIDE vs EDOXABAN