Does DUPILUMAB Cause Incorrect dose administered by device? 302 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 302 reports of Incorrect dose administered by device have been filed in association with DUPILUMAB (Dupixent). This represents 0.1% of all adverse event reports for DUPILUMAB.
302
Reports of Incorrect dose administered by device with DUPILUMAB
0.1%
of all DUPILUMAB reports
1
Deaths
5
Hospitalizations
How Dangerous Is Incorrect dose administered by device From DUPILUMAB?
Of the 302 reports, 1 (0.3%) resulted in death, 5 (1.7%) required hospitalization.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 302 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 Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which DUPILUMAB Alternatives Have Lower Incorrect dose administered by device Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE