Does IDURSULFASE Cause Device issue? 65 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 65 reports of Device issue have been filed in association with IDURSULFASE (ELAPRASE). This represents 2.0% of all adverse event reports for IDURSULFASE.
65
Reports of Device issue with IDURSULFASE
2.0%
of all IDURSULFASE reports
8
Deaths
36
Hospitalizations
How Dangerous Is Device issue From IDURSULFASE?
Of the 65 reports, 8 (12.3%) resulted in death, 36 (55.4%) required hospitalization, and 1 (1.5%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IDURSULFASE. However, 65 reports have been filed with the FAERS database.
What Other Side Effects Does IDURSULFASE Cause?
Pyrexia (524)
Product dose omission issue (450)
Inappropriate schedule of product administration (371)
Cough (263)
Infusion related reaction (241)
Pneumonia (232)
Death (222)
Dyspnoea (202)
Influenza (200)
Covid-19 (197)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which IDURSULFASE Alternatives Have Lower Device issue Risk?
IDURSULFASE vs IFOSFAMIDE
IDURSULFASE vs IGURATIMOD
IDURSULFASE vs ILOPERIDONE
IDURSULFASE vs ILOPROST
IDURSULFASE vs IMATINIB