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EMA Product

Dzuveo

Product approved by European Medicines Agency (EU)

Basic Information

Dzuveo

Regulatory Information

EMEA/H/C/004335

Authorised

June 25, 2018

April 26, 2018

8

September 12, 2024

Company Information

France

Laboratoire Aguettant 1, rue Alexander Fleming 69007 Lyon

Laboratoire Aguettant

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Dzuveo is indicated for the management of acute moderate to severe pain in adult patients.

Overview Summary

Dzuveo is an opioid pain medicine used to treat moderate to severe pain in adults. It is a ‘hybrid medicine’. This means that it is similar to a ‘reference medicine’ (called Sufenta Forte) containing the same active substance. The difference between the products is that Dzuveo is available as sublingual tablets (tablets to be dissolved under the tongue) while the reference medicine is a solution for injection. Dzuveo contains the active substance sufentanil.

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