Does DUPILUMAB Cause Product use issue? 10,575 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10,575 reports of Product use issue have been filed in association with DUPILUMAB (Dupixent). This represents 2.8% of all adverse event reports for DUPILUMAB.
10,575
Reports of Product use issue with DUPILUMAB
2.8%
of all DUPILUMAB reports
42
Deaths
691
Hospitalizations
How Dangerous Is Product use issue From DUPILUMAB?
Of the 10,575 reports, 42 (0.4%) resulted in death, 691 (6.5%) required hospitalization, and 11 (0.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 10,575 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 Product use issue?
INFLIXIMAB (12,752)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
CETIRIZINE (5,771)
Which DUPILUMAB Alternatives Have Lower Product use issue Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE