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Adverse events should be reported. United Kingdom Reporting forms and information can be found at Yellow Card | Making medicines and medical devices safer 3 or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to Galderma (UK) Ltd: E-mail: medinfo.uk@galderma.com Tel: +44 (0)300 3035674

 

▼This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. See ‘Undesirable Effects’ for how to report adverse reactions.

 

Link to PI & AE:
Relfydess Botulinum toxin type A solution for injection PI UK March 2025.pdf

 

This website is intended for Healthcare Practitioners only.

This website is created and funded by Galderma

 

 DOP June 2025 - UKI-REL-2500121

 

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