Does DUPILUMAB Cause Product preparation error? 2,707 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), 2,707 reports of Product preparation error have been filed in association with DUPILUMAB (Dupixent). This represents 0.7% of all adverse event reports for DUPILUMAB.
2,707
Reports of Product preparation error with DUPILUMAB
0.7%
of all DUPILUMAB reports
1
Deaths
52
Hospitalizations
How Dangerous Is Product preparation error From DUPILUMAB?
Of the 2,707 reports, 1 (0.0%) resulted in death, 52 (1.9%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 2,707 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
SODIUM OXYBATE (222)
Which DUPILUMAB Alternatives Have Lower Product preparation error Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE