Does ECALLANTIDE Cause Device issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device issue have been filed in association with ECALLANTIDE (Kalbitor). This represents 0.7% of all adverse event reports for ECALLANTIDE.
8
Reports of Device issue with ECALLANTIDE
0.7%
of all ECALLANTIDE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device issue From ECALLANTIDE?
Of the 8 reports, 3 (37.5%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECALLANTIDE. However, 8 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 Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ECALLANTIDE Alternatives Have Lower Device issue Risk?
ECALLANTIDE vs ECONAZOLE
ECALLANTIDE vs ECULIZUMAB
ECALLANTIDE vs EDARAVONE
ECALLANTIDE vs EDETATE
ECALLANTIDE vs EDOXABAN