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This promotional hub has been developed by Bayer plc and Bayer products are discussed. Bayer has fully funded the hub and is responsible for the content, logistics and selection of speakers. OmniaMed Communications has provided editorial, marketing and logistical support. © 2023 Bayer plc

Click here for Great Britain Prescribing Information for Kerendia (finerenone). Adverse Event Reporting details can be found at the bottom of the page

Video resources

Kerendia (finerenone) is indicated for the treatment of chronic kidney disease (CKD) (stage 3 and 4 with albuminuria) associated with type 2 diabetes (T2D) in adults.

Short Videos from our Keeping Up With the Kidneys series

14 minutes

Primary care as the gatekeeper in CKD: The need for collaboration with nephrologists

12 minutes

Finerenone : An update on guidelines and practical implementation

Play Video

8 minutes

Management of CKD in Primary & Secondary Care

Click here for Great Britain Prescribing Information for Kerendia (finerenone). Adverse Event Reporting details can be found at the bottom of the page

CKD bitesize

Play Video

4 minutes

Burden of diabetic kidney disease (DKD)

Play Video

3 minutes

CKD: The importance of early diagnosis

Play Video

2 minutes

CKD: The importance of urine albumin creatinine ratio (UACR) testing

Click here for Great Britain Prescribing Information for Kerendia (finerenone). Adverse Event Reporting details can be found at the bottom of the page

Play Video

6 minutes

Identifying CKD in primary care

Play Video

4 minutes

The Kidney Failure Risk Equation (KFRE)

Play Video

5 minutes

Effective management of hyperkalaemia

Click here for Great Britain Prescribing Information for Kerendia (finerenone). Adverse Event Reporting details can be found at the bottom of the page

Play Video

2 minutes

Kerendia (finerenone): Clinical data FIDELIO-DKD

Play Video

6 minutes

CKD as a risk factor for cardiovascular disease

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Play Video

9 minutes

The FIDELIO-DKD trial

Click here for Great Britain Prescribing Information for Kerendia (finerenone). Adverse Event Reporting details can be found at the bottom of the page

On Demand Webinars

Play Video

48 minutes

Time to act in diabetic kidney disease

Professor Philip Kalra and Dr Arif Khwaja discuss models of care for people with T2D and CKD, including NHS prevention strategies such as CVDPREVENT, and the implications of the Renal Services Transformation Programme for this population. Practical case studies will be introduced during the video to illustrate treatment and referral decisions for these patients.

Click here for Great Britain Prescribing Information for Kerendia (finerenone). Adverse Event Reporting details can be found at the bottom of the page

Filling in the gaps in the management of diabetic kidney disease

Professor Philip Kalra and Professor Smeeta Sinha discuss the potential role of Kerendia▼ (finerenone) in optimising the diabetic kidney disease (DKD) patient pathway, from early patient identification and initiation of treatment, to knowing how to manage hyperkalaemia and when to refer to a nephrologist.

Play Video

45 minutes

Click here for Great Britain Prescribing Information for Kerendia (finerenone). Adverse Event Reporting details can be found at the bottom of the page
Play Video

32 minutes

A treatment option for delaying the progression of chronic kidney disease in adults with type 2 diabetes

Professor Philip Kalra and Dr Kieran McCafferty examine the burden of chronic kidney disease (CKD) in adults with type 2 diabetes (T2D), assess the clinical trial data for Kerendia▼ (finerenone) and its impact on the progression of CKD associated with T2D, and outline prescribing considerations for Kerendia in people with CKD associated with T2D.

Click here for Great Britain Prescribing Information for Kerendia (finerenone). Adverse Event Reporting details can be found at the bottom of the page

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Click here for Great Britain Prescribing Information for Kerendia (finerenone).
Reporting adverse events and quality complaints ▼ This medicine is subject to additional monitoring. This will allow quick identification of new safety information. Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Bayer plc. If you want to report an adverse event or quality complaint, reports can be directed to: Tel: 01182063500 or email: [email protected] Further information is available on the “contact” tab at www.bayer.co.uk.

PP-KER-GB-0531 | October 2023

This promotional hub has been developed by Bayer plc and Bayer products are discussed. Bayer has fully funded the hub and is responsible for the content, logistics and selection of speakers.
OmniaMed Communications has provided editorial, marketing and logistical support.
© 2023 Bayer plc

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Prescribing information for Great Britain and Northern Ireland
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].


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