Does DUPILUMAB Cause Accidental exposure to product? 10,747 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10,747 reports of Accidental exposure to product have been filed in association with DUPILUMAB (Dupixent). This represents 2.8% of all adverse event reports for DUPILUMAB.
10,747
Reports of Accidental exposure to product with DUPILUMAB
2.8%
of all DUPILUMAB reports
10
Deaths
169
Hospitalizations
How Dangerous Is Accidental exposure to product From DUPILUMAB?
Of the 10,747 reports, 10 (0.1%) resulted in death, 169 (1.6%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Accidental exposure to product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 10,747 reports have been filed with the FAERS database.
What Other Side Effects Does DUPILUMAB Cause?
Pruritus (44,279)
Dermatitis atopic (33,670)
Product use in unapproved indication (33,452)
Rash (30,895)
Injection site pain (27,799)
Drug ineffective (23,712)
Dry skin (20,239)
Eczema (20,020)
Product dose omission issue (18,189)
Condition aggravated (16,459)
What Other Drugs Cause Accidental exposure to product?
EVOLOCUMAB (16,160)
ERENUMAB-AOOE (9,923)
ETANERCEPT (6,065)
PEGFILGRASTIM (4,967)
GUSELKUMAB (2,941)
SECUKINUMAB (2,397)
GOLIMUMAB (1,578)
USTEKINUMAB (1,352)
FREMANEZUMAB-VFRM (1,346)
DENOSUMAB (1,330)
Which DUPILUMAB Alternatives Have Lower Accidental exposure to product Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE