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GP Notebook

This promotional website has been developed, organised and funded by Boehringer Ingelheim.​

Did you know?

In a study of 11,000 Muslims with type 2 diabetes, 79% fasted during Ramadan despite being exempted due to their medical condition6

Our most popular learning modules

Proven efficacy vs placebo1,7

Proven efficacy vs placebo1,7: The efficacy and safety of 5 mg linagliptin was evaluated in eight phase III randomised controlled trials. Linagliptin once daily demonstrated clinically significant improvements in glycaemic control vs placebo or comparator.1

Demonstrated CV and kidney safety profile

Long-term cardiovascular and kidney safety profile of TRAJENTA® has been demonstrated in two cardiovascular outcome trials.8-14 As TRAJENTA® is primarily excreted via the bile, it is suitable for a broad range of adults with type 2 diabetes independent of renal function.1

Unique convenience of one dose, once daily1

The recommended dose of TRAJENTA® for adult patients with type 2 diabetes is 5 mg once daily, independent of renal and hepatic function, body mass index, age, ethnicity, background type 2 diabetes therapy, and disease duration.1,14

Webinar

Sarah Jarvis

Kevin Fernando

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Join our faculty as they discuss the role of clinical inertia in the suboptimal achievement of treatment targets and share practical tips for addressing this topic with your adult type 2 diabetes patients

References:
  1. TRAJENTA® (linagliptin) Summary of Product Characteristics (SmPC).*
  2. Sitagliptin SmPC.*
  3. Vildagliptin SmPC.*
  4. Saxagliptin SmPC.*
  5. Alogliptin SmPC.**
  6. Salti I, et al. Diabetes Care. 2004;27:2306-11
  7. McGill JB, et al. Diabetes Care. 2013;36:237–44.
  8. Rosenstock J, et al. Cardiovasc Diabetol. 2018;17:39.
  9. Rosenstock J, et al. JAMA. 2019;321:69–79.
  10. Cooper M, et al. Diabetes Obes Metab. 2020;22:1062–73.
  11. Marx N, et al. Diab Vasc Res. 2015;12:164–74.
  1. Rosenstock J, et al. JAMA. 2019;322:1155–66.
  2. Espeland MA, et al. Diabetes Obes Metab. 2021;23:569–80.
  3. Lajara R, et al. Clin Ther. 2014;36:1595–605.

*Summary of Product Characteristics for Trajenta, sitagliptin, vildagliptin and saxagliptin are available at: https://www.medicines.org.uk (GB), https://www.emcmedicines.com/en-GB/northernireland/ (NI) and https://www.medicines.ie/ (ROI).

**Summary of Product Characteristics for alogliptin are available at: https://www.medicines.org.uk (GB) and https://www.emcmedicines.com/en-GB/northernireland/ (NI).

Prescribing information for Great Britain and Northern Ireland and the Republic of Ireland.

Trajenta is indicated in adults with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control as:
• monotherapy when metformin is inappropriate due to intolerance, or contraindicated due to renal impairment
• in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control

The content has been reviewed and approved by the sponsoring company prior to its publication. Editorial support for this website has been provided by
OmniaMed Communications.

Adverse events should be reported. Reporting forms and information can be found at https://www.mhra.gov.uk/yellowcard (UK) or https://www.hpra.ie/homepage/about-us/report-an-issue (IRE). Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 0800 328 1627 (freephone) (UK) or 01 2913960 (IRE), Fax: +44 1344 742661, or by e-mail: [email protected].

PC-GB-106627 V6 | December 2023

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