Does IDURSULFASE Cause Incorrect product administration duration? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Incorrect product administration duration have been filed in association with IDURSULFASE (ELAPRASE). This represents 0.5% of all adverse event reports for IDURSULFASE.
15
Reports of Incorrect product administration duration with IDURSULFASE
0.5%
of all IDURSULFASE reports
1
Deaths
7
Hospitalizations
How Dangerous Is Incorrect product administration duration From IDURSULFASE?
Of the 15 reports, 1 (6.7%) resulted in death, 7 (46.7%) required hospitalization, and 1 (6.7%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IDURSULFASE. However, 15 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which IDURSULFASE Alternatives Have Lower Incorrect product administration duration Risk?
IDURSULFASE vs IFOSFAMIDE
IDURSULFASE vs IGURATIMOD
IDURSULFASE vs ILOPERIDONE
IDURSULFASE vs ILOPROST
IDURSULFASE vs IMATINIB