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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 Product administration error? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with AGALSIDASE BETA (Fabrazyme). This represents 0.1% of all adverse event reports for AGALSIDASE BETA.

5
Reports of Product administration error with AGALSIDASE BETA
0.1%
of all AGALSIDASE BETA reports
0
Deaths
3
Hospitalizations

How Dangerous Is Product administration error From AGALSIDASE BETA?

Of the 5 reports, 3 (60.0%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AGALSIDASE BETA. However, 5 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 Product administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which AGALSIDASE BETA Alternatives Have Lower Product administration error 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 Product administration error Reports All Drugs Causing Product administration error AGALSIDASE BETA Demographics