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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SEBELIPASE ALFA Cause Hypersensitivity? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Hypersensitivity have been filed in association with SEBELIPASE ALFA (KANUMA). This represents 2.3% of all adverse event reports for SEBELIPASE ALFA.

14
Reports of Hypersensitivity with SEBELIPASE ALFA
2.3%
of all SEBELIPASE ALFA reports
0
Deaths
2
Hospitalizations

How Dangerous Is Hypersensitivity From SEBELIPASE ALFA?

Of the 14 reports, 2 (14.3%) required hospitalization, and 1 (7.1%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for SEBELIPASE ALFA.

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 Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which SEBELIPASE ALFA Alternatives Have Lower Hypersensitivity Risk?

SEBELIPASE ALFA vs SECNIDAZOLE SEBELIPASE ALFA vs SECUKINUMAB SEBELIPASE ALFA vs SELADELPAR LYSINE SEBELIPASE ALFA vs SELEGILINE SEBELIPASE ALFA vs SELENIUM

Related Pages

SEBELIPASE ALFA Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity SEBELIPASE ALFA Demographics