Does IDURSULFASE Cause Device dislocation? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Device dislocation have been filed in association with IDURSULFASE (ELAPRASE). This represents 0.6% of all adverse event reports for IDURSULFASE.
20
Reports of Device dislocation with IDURSULFASE
0.6%
of all IDURSULFASE reports
2
Deaths
15
Hospitalizations
How Dangerous Is Device dislocation From IDURSULFASE?
Of the 20 reports, 2 (10.0%) resulted in death, 15 (75.0%) required hospitalization, and 3 (15.0%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IDURSULFASE. However, 20 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 dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which IDURSULFASE Alternatives Have Lower Device dislocation Risk?
IDURSULFASE vs IFOSFAMIDE
IDURSULFASE vs IGURATIMOD
IDURSULFASE vs ILOPERIDONE
IDURSULFASE vs ILOPROST
IDURSULFASE vs IMATINIB