Does DUPILUMAB Cause Wrong technique in product usage process? 781 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 781 reports of Wrong technique in product usage process have been filed in association with DUPILUMAB (Dupixent). This represents 0.2% of all adverse event reports for DUPILUMAB.
781
Reports of Wrong technique in product usage process with DUPILUMAB
0.2%
of all DUPILUMAB reports
0
Deaths
15
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DUPILUMAB?
Of the 781 reports, 15 (1.9%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 781 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DUPILUMAB Alternatives Have Lower Wrong technique in product usage process Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE