Does AGALSIDASE BETA Cause Product dose omission in error? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product dose omission in error have been filed in association with AGALSIDASE BETA (Fabrazyme). This represents 0.2% of all adverse event reports for AGALSIDASE BETA.
14
Reports of Product dose omission in error with AGALSIDASE BETA
0.2%
of all AGALSIDASE BETA reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission in error From AGALSIDASE BETA?
Of the 14 reports, 2 (14.3%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AGALSIDASE BETA. However, 14 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 dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which AGALSIDASE BETA Alternatives Have Lower Product dose omission in error Risk?
AGALSIDASE BETA vs AGOMELATINE
AGALSIDASE BETA vs ALAWAY
AGALSIDASE BETA vs ALBENDAZOLE
AGALSIDASE BETA vs ALBIGLUTIDE
AGALSIDASE BETA vs ALBUMIN