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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 Condition aggravated? 179 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 179 reports of Condition aggravated have been filed in association with AGALSIDASE BETA (Fabrazyme). This represents 2.8% of all adverse event reports for AGALSIDASE BETA.

179
Reports of Condition aggravated with AGALSIDASE BETA
2.8%
of all AGALSIDASE BETA reports
22
Deaths
69
Hospitalizations

How Dangerous Is Condition aggravated From AGALSIDASE BETA?

Of the 179 reports, 22 (12.3%) resulted in death, 69 (38.5%) required hospitalization, and 1 (0.6%) 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 AGALSIDASE BETA. However, 179 reports have been filed with the FAERS database.

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 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 AGALSIDASE BETA Alternatives Have Lower Condition aggravated 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 Condition aggravated Reports All Drugs Causing Condition aggravated AGALSIDASE BETA Demographics