Does DUPILUMAB Cause Impaired quality of life? 3,945 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,945 reports of Impaired quality of life have been filed in association with DUPILUMAB (Dupixent). This represents 1.0% of all adverse event reports for DUPILUMAB.
3,945
Reports of Impaired quality of life with DUPILUMAB
1.0%
of all DUPILUMAB reports
5
Deaths
306
Hospitalizations
How Dangerous Is Impaired quality of life From DUPILUMAB?
Of the 3,945 reports, 5 (0.1%) resulted in death, 306 (7.8%) required hospitalization, and 2 (0.1%) were considered life-threatening.
Is Impaired quality of life Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUPILUMAB. However, 3,945 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 Impaired quality of life?
DOCETAXEL (3,714)
ADALIMUMAB (725)
OXYCODONE (468)
INFLIXIMAB (447)
PREDNISONE (430)
VEDOLIZUMAB (372)
METHOTREXATE (279)
MESALAMINE (264)
BUDESONIDE (229)
ACETAMINOPHEN\OXYCODONE (203)
Which DUPILUMAB Alternatives Have Lower Impaired quality of life Risk?
DUPILUMAB vs DURAGESIC
DUPILUMAB vs DUROGESIC
DUPILUMAB vs DUROTEP MT
DUPILUMAB vs DURVALUMAB
DUPILUMAB vs DUTASTERIDE