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This website contains promotional content and is intended for Healthcare Professionals based in the United Kingdom only. Some content may only be relevant to HCPs practising in Great Britain (England, Scotland and Wales) according to product availability. This website is optimised for desktop use, and some features may perform differently on mobile devices.

Adverse event reporting can be found at the bottom of the page.

Praluent logo

Praluent® can be injected subcutaneously into the thigh, abdomen or upper arm. Patients should rotate the injection site with each injection.1

Praluent Image

Download the below leaflet to read how to administer Praluent

Download

Watch this video to see how to administer Praluent

Praluent®

Find more information on Indication, Administration and Mechanism of Action and watch videos about Praluent®.

Patient Website

Find resources and support for your patients on Praluent®. Find useful links about how patients can manage their cholesterol.

Get in touch with the Dyslipidaemia Team
References
  1. Praluent (alirocumab). Summary of Product Characteristics, Sanofi. 2025.
  2. Frias JP, Koren MJ, Loizeau V, et al. The SYDNEY Device Study: A Multicenter, Randomized, Open-label Usability Study of a 2-mL Alirocumab Autoinjector Device. Clinical Therapeutics. 2020; 42(1):94-107.
  3. Praluent (alirocumab) Patient Information Leaflet, 150mg. Sanofi, 2026.
  4. Praluent (alirocumab) Patient Information Leaflet, 300mg. Sanofi, 2026.
  5. Tatlock S, et al. Value Health 2017;20:430–440.
  6. Roth E, et al. Clin Ther 2015;37(9):1945–1954.

MAT-XU-2503036 (v2.0) Date of Preparation: March 2026  


Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to the Sanofi drug safety department on Tel: +44 (0) 800 0902 314. Alternatively, send via email to UK-drugsafety@sanofi.com