Does CONESTAT ALFA Cause Intentional product use issue? 227 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 227 reports of Intentional product use issue have been filed in association with CONESTAT ALFA (Ruconest). This represents 15.1% of all adverse event reports for CONESTAT ALFA.
227
Reports of Intentional product use issue with CONESTAT ALFA
15.1%
of all CONESTAT ALFA reports
2
Deaths
35
Hospitalizations
How Dangerous Is Intentional product use issue From CONESTAT ALFA?
Of the 227 reports, 2 (0.9%) resulted in death, 35 (15.4%) required hospitalization, and 2 (0.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CONESTAT ALFA. However, 227 reports have been filed with the FAERS database.
What Other Side Effects Does CONESTAT ALFA Cause?
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)
Product dose omission issue (46)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which CONESTAT ALFA Alternatives Have Lower Intentional product use issue Risk?
CONESTAT ALFA vs COPANLISIB
CONESTAT ALFA vs COPAXONE
CONESTAT ALFA vs COPEGUS
CONESTAT ALFA vs COPPER
CONESTAT ALFA vs CORDARONE