defatted powder of Arachis hypogaea L., semen (peanuts)

This medicine is authorised for use in the European Union.


Palforzia is a medicine for treating peanut allergy in children from 4 to 17 years of age and patients who become adults whilst on treatment. While taking this medicine, patients continue avoiding peanuts.

Palforzia contains peanut powder.

This EPAR was last updated on 19/09/2022

Authorisation details

Product details
Agency product number
Active substance
defatted powder of Arachis hypogaea L., semen (peanuts)
International non-proprietary name (INN) or common name
defatted powder of Arachis hypogaea L., semen (peanuts)
Therapeutic area (MeSH)
Peanut Hypersensitivity
Anatomical therapeutic chemical (ATC) code
Additional monitoringAdditional monitoring

This medicine is under additional monitoring, meaning that it is monitored even more intensively than other medicines. For more information, see Medicines under additional monitoring.

Publication details
Marketing-authorisation holder
Aimmune Therapeutics Ireland Limited
Date of issue of marketing authorisation valid throughout the European Union
Contact address

Block B The Crescent Building
Northwood Crescent Northwood
Dublin 9 Co.
Dublin D09 C6X8

Product information

19/09/2022 Palforzia - EMEA/H/C/004917 - N/0011

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Product information documents contain:

You can find product information documents for centrally authorised human medicines on this website. For centrally authorised veterinary medicines authorised or updated from February 2022, see the Veterinary Medicines Information website.

Pharmacotherapeutic group


Therapeutic indication

Palforzia is indicated for the treatment of patients aged 4 to 17 years with a confirmed diagnosis of peanut allergy. Palforzia may be continued in patients 18 years of age and older.

Palforzia should be used in conjunction with a peanut-avoidant diet.

Assessment history

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