Does IDURSULFASE Cause Condition aggravated? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Condition aggravated have been filed in association with IDURSULFASE (ELAPRASE). This represents 1.6% of all adverse event reports for IDURSULFASE.
52
Reports of Condition aggravated with IDURSULFASE
1.6%
of all IDURSULFASE reports
15
Deaths
32
Hospitalizations
How Dangerous Is Condition aggravated From IDURSULFASE?
Of the 52 reports, 15 (28.8%) resulted in death, 32 (61.5%) required hospitalization, and 4 (7.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IDURSULFASE. However, 52 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which IDURSULFASE Alternatives Have Lower Condition aggravated Risk?
IDURSULFASE vs IFOSFAMIDE
IDURSULFASE vs IGURATIMOD
IDURSULFASE vs ILOPERIDONE
IDURSULFASE vs ILOPROST
IDURSULFASE vs IMATINIB