Does SEBELIPASE ALFA Cause Condition aggravated? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Condition aggravated have been filed in association with SEBELIPASE ALFA (KANUMA). This represents 2.0% of all adverse event reports for SEBELIPASE ALFA.
12
Reports of Condition aggravated with SEBELIPASE ALFA
2.0%
of all SEBELIPASE ALFA reports
2
Deaths
5
Hospitalizations
How Dangerous Is Condition aggravated From SEBELIPASE ALFA?
Of the 12 reports, 2 (16.7%) resulted in death, 5 (41.7%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEBELIPASE ALFA. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does SEBELIPASE ALFA Cause?
Pyrexia (59)
Diarrhoea (45)
Vomiting (42)
Off label use (38)
Drug ineffective (27)
Headache (26)
Low density lipoprotein increased (22)
Malaise (22)
Fatigue (19)
Infusion related reaction (19)
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 SEBELIPASE ALFA Alternatives Have Lower Condition aggravated Risk?
SEBELIPASE ALFA vs SECNIDAZOLE
SEBELIPASE ALFA vs SECUKINUMAB
SEBELIPASE ALFA vs SELADELPAR LYSINE
SEBELIPASE ALFA vs SELEGILINE
SEBELIPASE ALFA vs SELENIUM