Does CONESTAT ALFA Cause Complication associated with device? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Complication associated with device have been filed in association with CONESTAT ALFA (Ruconest). This represents 1.3% of all adverse event reports for CONESTAT ALFA.
19
Reports of Complication associated with device with CONESTAT ALFA
1.3%
of all CONESTAT ALFA reports
0
Deaths
5
Hospitalizations
How Dangerous Is Complication associated with device From CONESTAT ALFA?
Of the 19 reports, 5 (26.3%) required hospitalization, and 1 (5.3%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CONESTAT ALFA. However, 19 reports have been filed with the FAERS database.
What Other Side Effects Does CONESTAT ALFA Cause?
Intentional product use issue (227)
Condition aggravated (166)
Weight fluctuation (125)
Product use in unapproved indication (97)
Drug ineffective (94)
Vascular access site complication (90)
Underdose (74)
Weight decreased (74)
Weight increased (74)
Insurance issue (48)
What Other Drugs Cause Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which CONESTAT ALFA Alternatives Have Lower Complication associated with device Risk?
CONESTAT ALFA vs COPANLISIB
CONESTAT ALFA vs COPAXONE
CONESTAT ALFA vs COPEGUS
CONESTAT ALFA vs COPPER
CONESTAT ALFA vs CORDARONE