Does GALSULFASE Cause Product dose omission? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Product dose omission have been filed in association with GALSULFASE (NAGLAZYME). This represents 2.1% of all adverse event reports for GALSULFASE.
59
Reports of Product dose omission with GALSULFASE
2.1%
of all GALSULFASE reports
0
Deaths
25
Hospitalizations
How Dangerous Is Product dose omission From GALSULFASE?
Of the 59 reports, 25 (42.4%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GALSULFASE. However, 59 reports have been filed with the FAERS database.
What Other Side Effects Does GALSULFASE Cause?
Pyrexia (338)
Pneumonia (197)
Cough (181)
Dyspnoea (154)
Spinal cord compression (108)
Vomiting (106)
Oxygen saturation decreased (100)
Fatigue (92)
Pain (81)
Headache (75)
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 GALSULFASE Alternatives Have Lower Product dose omission Risk?
GALSULFASE vs GAMMAGARD LIQUID
GALSULFASE vs GANAXOLONE
GALSULFASE vs GANCICLOVIR
GALSULFASE vs GANIRELIX
GALSULFASE vs GATIFLOXACIN