Does CONESTAT ALFA Cause Condition aggravated? 166 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 166 reports of Condition aggravated have been filed in association with CONESTAT ALFA (Ruconest). This represents 11.0% of all adverse event reports for CONESTAT ALFA.
166
Reports of Condition aggravated with CONESTAT ALFA
11.0%
of all CONESTAT ALFA reports
2
Deaths
23
Hospitalizations
How Dangerous Is Condition aggravated From CONESTAT ALFA?
Of the 166 reports, 2 (1.2%) resulted in death, 23 (13.9%) required hospitalization, and 2 (1.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CONESTAT ALFA. However, 166 reports have been filed with the FAERS database.
What Other Side Effects Does CONESTAT ALFA Cause?
Intentional product use issue (227)
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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CONESTAT ALFA Alternatives Have Lower Condition aggravated Risk?
CONESTAT ALFA vs COPANLISIB
CONESTAT ALFA vs COPAXONE
CONESTAT ALFA vs COPEGUS
CONESTAT ALFA vs COPPER
CONESTAT ALFA vs CORDARONE