Does DUPILUMAB Cause Device defective? 281 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 281 reports of Device defective have been filed in association with DUPILUMAB (Dupixent). This represents 0.1% of all adverse event reports for DUPILUMAB.
281
Reports of Device defective with DUPILUMAB
0.1%
of all DUPILUMAB reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device defective From DUPILUMAB?
Of the 281 reports, 3 (1.1%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 281 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which DUPILUMAB Alternatives Have Lower Device defective Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE