Does AGALSIDASE BETA Cause Incorrect product administration duration? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Incorrect product administration duration have been filed in association with AGALSIDASE BETA (Fabrazyme). This represents 0.1% of all adverse event reports for AGALSIDASE BETA.
6
Reports of Incorrect product administration duration with AGALSIDASE BETA
0.1%
of all AGALSIDASE BETA reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From AGALSIDASE BETA?
Of the 6 reports, 1 (16.7%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AGALSIDASE BETA. However, 6 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which AGALSIDASE BETA Alternatives Have Lower Incorrect product administration duration Risk?
AGALSIDASE BETA vs AGOMELATINE
AGALSIDASE BETA vs ALAWAY
AGALSIDASE BETA vs ALBENDAZOLE
AGALSIDASE BETA vs ALBIGLUTIDE
AGALSIDASE BETA vs ALBUMIN