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This website is intended for healthcare professionals in KSA and UAE only.

The content provided is developed in accordance with local regulations and may not be applicable or compliant in other regions.

This website is intended for healthcare professionals in KSA and UAE only.
 The content provided is developed in accordance with local regulations and may not be applicable or compliant in other regions.

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Summary

One simple step to overall K+ control

Efficacy for all

Works from the 1st dose

Lowers serum K+ from the first dose, regardless of HK severity2

Sustained K+ Control

Proven to sustain K+ within normokalemia range over 52 weeks3

Proven efficacy in different patient profiles

Proven efficacy with concomitant RAASi use backed by 4 placebo-controlled trials across comorbidities,4–7 and in the real-world setting for haemodialysis patients8,9

Patient friendly

One sachet daily from the start

80–90% of patients need an 8.4 g sachet per day1,9

Odourless, taste-free

Proven in a palatability study to be a positive experience in terms of odour and taste9

Juice or soft food mixing options

Extra versatility to suit individual tastes1

Designed for tolerability

Na+ free exchange

Suitable for Na+ sensitive patients with no Na+ associated risk1

Minimal GI effects

Optimised physical characteristics to minimise undesirable GI effect1,10

References & footnotes

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Abbreviations

GI, gastrointestinal; HK, hyperkalemia; K+, potassium; Na+, sodium; RAASi, renin-angiotensin-aldosterone-system inhibitor; SAEs, serious adverse events.

References

  1. Veltassa Gulf SmPC. Veltassa KSA SmPC.
  2. Di Palo KE, et al. Assessment of Patiromer Monotherapy for Hyperkalemia in an Acute Care Setting. JAMA Netw Open 2022;5(1):e2145236.
  3. Bakris GL, et al. Effect of Patiromer on Serum Potassium Level in Patients With Hyperkalemia and Diabetic Kidney Disease. JAMA 2015;314(2):151–61.
  4. Butler J, et al. Patiromer for the management of hyperkalemia in heart failure with reduced ejection fraction: the DIAMOND trial. Eur J Hear Fail 2022;43(41):4362–73.
  5. Weir MR, et al. Patiromer in Patients with Kidney Disease and Hyperkalemia Receiving RAAS Inhibitors. N Engl J Med 2015;372(3):211–21.
  6. Agarwal R, et al. Patiromer versus placebo to enable spironolactone use in patients with resistant hypertension and chronic kidney disease (AMBER): a phase 2, randomised, double-blind, placebo-controlled trial. Lancet 2019;394(10208):1540–50.
  7. Pitt B, et al. Evaluation of the efficacy and safety of RLY5016, a polymeric potassium binder, in a double-blind, placebo-controlled study in patients with chronic heart failure (the PEARL-HF) trial. Eur Heart J 2011;32:820–28.
  8. Kovesdy CP, et al. Real-World Evaluation of Patiromer for the Treatment of Hyperkalemia in Hemodialysis Patients. Kidney Int Rep 2019;4(2):301–9.
  9. Brenner M, et al. Palatability Profile of Patiromer, a Once-Daily Oral Potassium Binder for the Treatment of Hyperkalemia. American Society of Health System Pharmacists Annual Meeting. December 4–8, 2016. Las Vegas, NV. Poster, P4-075.
  10. Li L, et al. Mechanism of Action and Pharmacology of Patiromer, a Nonabsorbed Cross-Linked Polymer That Lowers Serum Potassium Concentration in Patients With Hyperkalemia. J Card Pharmacol Ther 2016;21(5):456–65.

GCC-PAT-2500019 | Date of preparation: October 2025