Does IDURSULFASE Cause Product dose omission issue? 450 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 450 reports of Product dose omission issue have been filed in association with IDURSULFASE (ELAPRASE). This represents 14.1% of all adverse event reports for IDURSULFASE.
450
Reports of Product dose omission issue with IDURSULFASE
14.1%
of all IDURSULFASE reports
66
Deaths
247
Hospitalizations
How Dangerous Is Product dose omission issue From IDURSULFASE?
Of the 450 reports, 66 (14.7%) resulted in death, 247 (54.9%) required hospitalization, and 18 (4.0%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IDURSULFASE. However, 450 reports have been filed with the FAERS database.
What Other Side Effects Does IDURSULFASE Cause?
Pyrexia (524)
Inappropriate schedule of product administration (371)
Cough (263)
Infusion related reaction (241)
Pneumonia (232)
Death (222)
Dyspnoea (202)
Influenza (200)
Covid-19 (197)
Seizure (195)
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 IDURSULFASE Alternatives Have Lower Product dose omission issue Risk?
IDURSULFASE vs IFOSFAMIDE
IDURSULFASE vs IGURATIMOD
IDURSULFASE vs ILOPERIDONE
IDURSULFASE vs ILOPROST
IDURSULFASE vs IMATINIB