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Demonstrated safety profile

Adverse reactions occurring in ≥2% of DUPIXENT patients through Week 24 and greater than placebo (pooled safety across PRIME and PRIME2)1

aNasopharyngitis includes pharyngitis.

bConjunctivitis includes conjunctivitis and allergic conjunctivitis.

cHerpes infection includes oral herpes, genital herpes simplex, herpes zoster, and ophthalmic herpes zoster.

dDizziness includes dizziness postural, vertigo, and vertigo positional.

eMyalgia includes musculoskeletal pain and musculoskeletal chest pain.

Attributes and considerations

NOT AN
IMMUNOSUPPRESSANT
OR A STEROID1

NO KNOWN DRUG-TO-DRUG
INTERACTIONS1

Not metabolized through the liver or excreted through the kidneys

NO INITIAL LAB TESTING OR
ONGOING LAB MONITORING

according to the Prescribing Information1

NO BOXED WARNING1

Please see additional Warnings and Precautions in the
Prescribing Information and Important Safety Information below.

SELECT IMPORTANT SAFETY INFORMATION

WARNINGS AND PRECAUTIONS

  • Hypersensitivity: Hypersensitivity reactions, including anaphylaxis, acute generalized exanthematous pustulosis (AGEP), serum sickness or serum sickness-like reactions, angioedema, generalized urticaria, rash, erythema nodosum, and erythema multiforme have been reported. A case of AGEP was reported in an adult subject who participated in the bullous pemphigoid development program. If a clinically significant hypersensitivity reaction occurs, institute appropriate therapy and discontinue DUPIXENT.

Q2W, once every 2 weeks.