Azzalure treatment

Azzalure® is a European botulinum neurotoxin type A. The Azzalure brand is derived from Dysport®, which was first registered in 1990. Azzalure is intended for use in aesthetic medicine, whereas the Dysport brand is primarily used for medical treatments with therapeutic indications. Azzalure is mainly used to treat frown lines, forehead wrinkles, and crow’s feet.

Dysport botulinum toxin

Dysport was first registered by the manufacturer Ipsen in 1990 in the United Kingdom and has been available on the market for medical applications since 1991. Ipsen conducted extensive research on neurotoxins with the goal of providing functional treatment for patients with medical needs.

Dysport has received approvals worldwide for treating musculoskeletal or neurological muscle disorders. For example, it is indicated for adults following a stroke, traumatic brain injury, or multiple sclerosis (MS), and for children with spasticity.

For aesthetic use, Ipsen markets Dysport under the brand name Azzalure. Azzalure is exclusively distributed to Galderma, a pharmaceutical company specialising in dermatological treatments. Galderma manages the sales, information, and promotion of Azzalure in different countries.

Azzalure frown lines

Both Dysport and Azzalure are approved by the FDA (U.S. Food and Drug Administration) for various medical and cosmetic indications, including the treatment of frown lines. Globally, Dysport and Azzalure are referred to as BoNT-A® and measured in Speywood Units. Like all neurotoxins used in aesthetics, Azzalure® is a botulinum neurotoxin type A, the longest-studied serotype with hundreds of clinical studies confirming its efficacy and safety.

Scientific research consistently shows that Azzalure is safe and effective when administered by a qualified practitioner who follows established contraindications and proper guidelines for storage, preparation, sterility, injection materials, and technique.

Azzalure treatment appointment

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