Anpheros Search · Treatment

Alogliptin

Also known as: alogliptin benzoate · Vipidia

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In short

In the European Union, alogliptin is indicated in adults aged 18 years and older with type 2 diabetes mellitus to improve glycaemic control. It is used in combination with other glucose lowering medicinal products including insulin, when these, together with diet and exercise, do not provide adequate glycaemic control. Alogliptin has an approved use for type 2 diabetes mellitus.

Source: European Medicines Agency (EMA), Vipidia — EPAR, 21/07/2023. © European Medicines Agency. · Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

EMA
EMEA/H/C/002182

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

EMA (EU) Vipidia

Vipidia is indicated in adults aged 18 years and older with type 2 diabetes mellitus to improve glycaemic control in combination with other glucose lowering medicinal products including insulin, when these, together with diet and exercise, do not provide adequate glycaemic control (see sections 4.4, 4.5 and 5.1 for available data on different combinations).

Source: European Medicines Agency (EMA), Vipidia — EPAR, 21/07/2023. © European Medicines Agency.

Document date: 21/07/2023 · Official document →

Related terms in the cited sources

Has an official indication for

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What people report

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External resources

Questions

What is Alogliptin approved for in the European Union?

Vipidia is indicated in adults aged 18 years and older with type 2 diabetes mellitus to improve glycaemic control in combination with other glucose lowering medicinal products including insulin, when these, together with diet and exercise, do not provide adequate glycaemic control (see sections 4.4, 4.5 and 5.1 for available data on different combinations). (Source: European Medicines Agency (EMA), Vipidia — EPAR, 21/07/2023. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), Vipidia — EPAR, 21/07/2023. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →