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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 ALFA Cause Product dose omission issue? 20 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product dose omission issue have been filed in association with AGALSIDASE ALFA. This represents 18.5% of all adverse event reports for AGALSIDASE ALFA.

20
Reports of Product dose omission issue with AGALSIDASE ALFA
18.5%
of all AGALSIDASE ALFA reports
2
Deaths
16
Hospitalizations

How Dangerous Is Product dose omission issue From AGALSIDASE ALFA?

Of the 20 reports, 2 (10.0%) resulted in death, 16 (80.0%) required hospitalization.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AGALSIDASE ALFA. However, 20 reports have been filed with the FAERS database.

What Other Side Effects Does AGALSIDASE ALFA Cause?

Fatigue (40) Inappropriate schedule of product administration (40) Malaise (28) Headache (27) Cough (26) Nausea (26) Blood pressure decreased (25) Covid-19 (25) Dizziness (25) Pain (25)

What Other Drugs Cause Product dose omission issue?

DUPILUMAB (18,189) USTEKINUMAB (9,405) GUSELKUMAB (9,267) LENALIDOMIDE (8,145) MEPOLIZUMAB (5,873) TOFACITINIB (5,646) VOXELOTOR (5,122) BELIMUMAB (4,671) SECUKINUMAB (4,572) APREMILAST (4,460)

Which AGALSIDASE ALFA Alternatives Have Lower Product dose omission issue Risk?

AGALSIDASE ALFA vs AGALSIDASE BETA AGALSIDASE ALFA vs AGOMELATINE AGALSIDASE ALFA vs ALAWAY AGALSIDASE ALFA vs ALBENDAZOLE AGALSIDASE ALFA vs ALBIGLUTIDE

Related Pages

AGALSIDASE ALFA Full Profile All Product dose omission issue Reports All Drugs Causing Product dose omission issue AGALSIDASE ALFA Demographics