Does ECALLANTIDE Cause Wrong technique in product usage process? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Wrong technique in product usage process have been filed in association with ECALLANTIDE (Kalbitor). This represents 0.4% of all adverse event reports for ECALLANTIDE.
5
Reports of Wrong technique in product usage process with ECALLANTIDE
0.4%
of all ECALLANTIDE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ECALLANTIDE?
Of the 5 reports, 3 (60.0%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECALLANTIDE. However, 5 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ECALLANTIDE Alternatives Have Lower Wrong technique in product usage process Risk?
ECALLANTIDE vs ECONAZOLE
ECALLANTIDE vs ECULIZUMAB
ECALLANTIDE vs EDARAVONE
ECALLANTIDE vs EDETATE
ECALLANTIDE vs EDOXABAN