Does AGALSIDASE BETA Cause Product dose omission? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Product dose omission have been filed in association with AGALSIDASE BETA (Fabrazyme). This represents 0.9% of all adverse event reports for AGALSIDASE BETA.
57
Reports of Product dose omission with AGALSIDASE BETA
0.9%
of all AGALSIDASE BETA reports
0
Deaths
8
Hospitalizations
How Dangerous Is Product dose omission From AGALSIDASE BETA?
Of the 57 reports, 8 (14.0%) required hospitalization, and 1 (1.8%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AGALSIDASE BETA. However, 57 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which AGALSIDASE BETA Alternatives Have Lower Product dose omission Risk?
AGALSIDASE BETA vs AGOMELATINE
AGALSIDASE BETA vs ALAWAY
AGALSIDASE BETA vs ALBENDAZOLE
AGALSIDASE BETA vs ALBIGLUTIDE
AGALSIDASE BETA vs ALBUMIN