Does IDURSULFASE Cause Product administration error? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product administration error have been filed in association with IDURSULFASE (ELAPRASE). This represents 0.3% of all adverse event reports for IDURSULFASE.
10
Reports of Product administration error with IDURSULFASE
0.3%
of all IDURSULFASE reports
1
Deaths
3
Hospitalizations
How Dangerous Is Product administration error From IDURSULFASE?
Of the 10 reports, 1 (10.0%) resulted in death, 3 (30.0%) required hospitalization, and 1 (10.0%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IDURSULFASE. However, 10 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which IDURSULFASE Alternatives Have Lower Product administration error Risk?
IDURSULFASE vs IFOSFAMIDE
IDURSULFASE vs IGURATIMOD
IDURSULFASE vs ILOPERIDONE
IDURSULFASE vs ILOPROST
IDURSULFASE vs IMATINIB