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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 AGALSIDASE BETA Cause Hypersensitivity? 68 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Hypersensitivity have been filed in association with AGALSIDASE BETA (Fabrazyme). This represents 1.1% of all adverse event reports for AGALSIDASE BETA.

68
Reports of Hypersensitivity with AGALSIDASE BETA
1.1%
of all AGALSIDASE BETA reports
2
Deaths
15
Hospitalizations

How Dangerous Is Hypersensitivity From AGALSIDASE BETA?

Of the 68 reports, 2 (2.9%) resulted in death, 15 (22.1%) required hospitalization, and 1 (1.5%) 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 AGALSIDASE BETA.

What Other Side Effects Does AGALSIDASE BETA Cause?

Malaise (409) Pain (395) Pyrexia (362) Fatigue (338) Nausea (303) Weight decreased (272) Headache (269) Dyspnoea (266) Chills (259) Vomiting (244)

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 AGALSIDASE BETA Alternatives Have Lower Hypersensitivity Risk?

AGALSIDASE BETA vs AGOMELATINE AGALSIDASE BETA vs ALAWAY AGALSIDASE BETA vs ALBENDAZOLE AGALSIDASE BETA vs ALBIGLUTIDE AGALSIDASE BETA vs ALBUMIN

Related Pages

AGALSIDASE BETA Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity AGALSIDASE BETA Demographics