This website is intended for UK Healthcare Professionals only. Other UK residents please visit astrazeneca.co.uk
Prescribing information can be found in the middle of the page and adverse event reporting information at the bottom of the page.
Welcome to this UK AstraZeneca produced and funded website
This website is intended for UK Healthcare Professionals only.
The website contains both promotional and non-promotional content.
If you are a patient or a carer of a patient prescribed an AstraZeneca product, please visit myazmed.co.uk
For any other UK residents please visit astrazeneca.co.uk
This website is intended for UK Healthcare Professionals only. Other UK residents please visit astrazeneca.co.uk
Prescribing information can be found in the middle of the page and adverse event reporting information at the bottom of the page.
Renal diseases are increasingly affecting the UK population, with profound implications for public health and quality of life. These conditions are often underdiagnosed, leading to delayed interventions and poorer outcomes. It is crucial to implement early diagnostic and proactive risk management strategies to slow disease progression and reduce the risk of developing comorbidities.1,2
We are committed to improving treatment and research in two critical aspects of renal health and its related complications: chronic kidney disease and hyperkalaemia.
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Chronic kidney disease (CKD) affects around 7.2 million people in the UK and there are approximately a million people living with undiagnosed CKD in England alone. It is well established that people from lower socio-economic groups and people from ethnic minority groups are more likely to develop CKD.
With better screening, early management, and innovative pharmacological therapies, CKD progression could be delayed and patients may enjoy healthier and more productive lives.2
Explore AstraZeneca’s option for managing CKD:
FORXIGA® (dapagliflozin)
FORXIGA® (dapagliflozin) is indicated for the treatment of CKD in adult patients *
FORXIGA® (dapagliflozin) Prescribing Information
* Dapagliflozin is not recommended in patients with an estimated glomerular filtration rate (eGFR) < 15 mL/min/1.73m2.
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Hyperkalaemia, defined as serum or plasma potassium ≥ 5.5 mmol/L, can be life-threatening. Patients with severe hyperkalaemia are most at risk of death, with an in-hospital mortality rate of around 31%.6
Certain CKD and heart failure medications, such as renin-angiotensin-aldosterone system inhibitors (RAASi), can cause high potassium levels, leading to a higher chance of developing hyperkalaemia.7
There is an urgent need for better hyperkalaemia treatment across patient populations to reduce mortality rates and cardiovascular complications.7 Current approaches often involve down-titration of RAASi therapy, which can increase the risk of death and prevent the achievement of guideline-directed medical therapy (GDMT). Improved management is crucial for effective cardiorenal protection.8
Explore AstraZeneca’s option for managing hyperkalaemia:
LOKELMA® (sodium zirconium cyclosilicate)
LOKLEMA® (sodium zirconium cyclosilicate) is indicated for the treatment of hyperkalaemia in adult patients
With the increased prevalence of risk factors such as diabetes and cardiovascular disease in an ageing population, the prevalence of CKD is also increasing.² This rise contributes to greater utilisation of healthcare resources for CKD, driving up costs.²
In 2023, the economic burden of CKD in the UK was estimated at £7.0 billion, including £6.4 billion in direct costs to the NHS, representing approximately 3.2% of its budget.³
Left untreated, CKD may cause the kidneys to stop working, which can lead to the need for dialysis or kidney transplant. This can cause a decline in a patient's quality of life.
At AstraZeneca, we are committed to transforming the management of CKD and hyperkalaemia by working in partnership with the NHS to help:
We are supporting boundary-pushing research across the full continuum of disease progression. We want to reframe practice to place an increased emphasis on early detection and diagnosis and we are committed to reducing disease progression to end-stage renal disease and the onset of other closely linked cardiovascular complications.
GB-63020 | DOP: January 2025
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to AstraZeneca by visiting https://contactazmedical.astrazeneca.com/ or by calling 0800 783 0033.