Does DUPILUMAB Cause Intentional product misuse? 1,436 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,436 reports of Intentional product misuse have been filed in association with DUPILUMAB (Dupixent). This represents 0.4% of all adverse event reports for DUPILUMAB.
1,436
Reports of Intentional product misuse with DUPILUMAB
0.4%
of all DUPILUMAB reports
1
Deaths
27
Hospitalizations
How Dangerous Is Intentional product misuse From DUPILUMAB?
Of the 1,436 reports, 1 (0.1%) resulted in death, 27 (1.9%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 1,436 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DUPILUMAB Alternatives Have Lower Intentional product misuse Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE