Does DUPILUMAB Cause Device use issue? 528 Reports in FDA Database
Visibly Younger Skin in Weeks
Synevra Lift & Lock — Swiss peptide serum + nutrients. 60-day money-back guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 528 reports of Device use issue have been filed in association with DUPILUMAB (Dupixent). This represents 0.1% of all adverse event reports for DUPILUMAB.
528
Reports of Device use issue with DUPILUMAB
0.1%
of all DUPILUMAB reports
1
Deaths
12
Hospitalizations
How Dangerous Is Device use issue From DUPILUMAB?
Of the 528 reports, 1 (0.2%) resulted in death, 12 (2.3%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 528 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 use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
LEVODOPA (443)
Which DUPILUMAB Alternatives Have Lower Device use issue Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE