Ireland's most popular source of accurate and reliable medicines information
Search 3283 medicines for SPCs, PILs and Educational Materials
Calling Doctors and Other Prescribers
Help shape the new medicines.ie website coming soon. Sign up to participate in upcoming user-testing sessions and contribute to the future of medicines information.
 DAC.webp)
 Ireland Limited.webp)
 July 2021_1625477146.webp){kind=logo}
 Ltd.webp)
_1580899259.webp)
 Limited.webp)
 Ltd.webp)
 Ltd.webp)
_1625736541.webp)
 Ltd.webp)
 Ltd.webp)
 Limited.webp)
 Limited.webp)
Latest medicine updates
- Avtozma 20 mg/mL concentrate for solution for infusion Celltrion Healthcare Ireland Ltd.
Updated - Comirnaty XFG 30 micrograms/dose dispersion for injection (frozen vials) Adults and adolescents from 12 years Pfizer Healthcare Ireland Unlimited Company
Updated - Comirnaty XFG 10 micrograms/dose dispersion for injection Infants and children 6 months to 11 years Pfizer Healthcare Ireland Unlimited Company
Updated - TOBI 300 mg/5 mL Nebuliser Solution Mylan IRE Healthcare Ltd
Updated - ZEPZELCA 2 mg powder for concentrate for solution for infusion/ZEPZELCA 4 mg powder for concentrate for solution for infusion Immedica (distributor)
New - Alkindi 0.5 mg granules in capsules for opening/Alkindi 1 mg granules in capsules for opening/Alkindi 2 mg granules in capsules for opening/Alkindi 5 mg granules in capsules for opening Immedica Pharma AB
New - ZITHROMAX CAPSULES 250MG Pfizer Healthcare Ireland Unlimited Company
Updated
About medicines.ie
Using medicines.ie
medicines.ie contains accurate, up-to-date, regulator-approved information on medicines available in Ireland. The site is designed to be a comprehensive and easily searchable source of medicines information in Ireland.
It is widely regarded as an invaluable reference source by healthcare professionals, the National Medicines Information Centre and the Department of Health.
The information for each product comes in the form of a Summary of Product Characteristics (SPC or SmPC) and Patient Information Leaflet (PIL) or Package Leaflet (PL), where relevant. These documents are approved by the medicines’ regulator ( HPRA or EMA ) as part of the process of authorising a medicine for sale or supply in Ireland.
medicines.ie is continuously updated by pharmaceutical companies when new medicines are launched or the information for an existing medicine changes. For human medicines not included in the medicines.ie database, but available on the European Medicines Agency (EMA) website, a button will redirect the user to the EMA website. A medicine included in the EMA database may not be currently available in the Irish market.