Is there an association between omeprazole and hyponatremia?

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Last updated: March 19, 2025View editorial policy

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From the Guidelines

There is no clear association between omeprazole and hyponatremia based on the provided evidence. The study referenced 1 does not mention hyponatremia as a potential side effect of omeprazole, instead focusing on its use in the treatment of chronic rhinosinusitis (CRS) and its potential association with an increased risk of cardiovascular disease.

Key Points to Consider

  • The provided study 1 does not directly address the question of an association between omeprazole and hyponatremia.
  • The study's primary focus is on the treatment of CRS and the potential risks associated with long-term use of proton pump inhibitors, such as cardiovascular disease.
  • Given the lack of direct evidence from the provided study 1, it is essential to consider other potential sources of information that may address the association between omeprazole and hyponatremia.

Clinical Implications

  • In clinical practice, when prescribing omeprazole or any other proton pump inhibitor, it is crucial to be aware of potential side effects, even if they are not directly mentioned in the provided evidence 1.
  • Monitoring patients for signs of hyponatremia, such as headache, confusion, or muscle weakness, especially in high-risk populations like the elderly or those on diuretics, is a prudent approach.
  • If hyponatremia is suspected, considering alternative treatments, like H2 blockers, and closely monitoring serum sodium levels may be necessary.

From the Research

Association between Omeprazole and Hyponatremia

  • There is evidence to suggest an association between omeprazole and hyponatremia, as reported in a case study where a 67-year-old male developed hyponatremia due to the syndrome of inappropriate antidiuretic hormone secretion secondary to omeprazole use 2.
  • A population-based case-control study found that newly initiated omeprazole use was associated with an increased risk of hospitalization due to hyponatremia, with an adjusted OR of 2.67 (95% CI: 2.37-3.01) 3.
  • Another study reviewed clinical information about the incidence of hyponatremia associated with specific drug treatment, including proton pump inhibitors like omeprazole, and discussed the underlying pathophysiologic mechanisms 4.

Clinical Implications

  • The association between omeprazole and hyponatremia highlights the importance of monitoring serum sodium levels in patients taking this medication, especially in those with a history of hyponatremia or at risk of developing it 2, 3.
  • Expert panel recommendations for the diagnosis, evaluation, and treatment of hyponatremia emphasize the need for awareness of medication-induced hyponatremia, including that caused by proton pump inhibitors like omeprazole 5.

Comparison with Other Proton Pump Inhibitors

  • The case study mentioned earlier also found that pantoprazole, another proton pump inhibitor, induced hyponatremia in the same patient, suggesting a class effect 2.
  • The population-based case-control study found that other proton pump inhibitors, such as esomeprazole and pantoprazole, were also associated with an increased risk of hospitalization due to hyponatremia, although the risk was lower compared to omeprazole 3.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

A review of drug-induced hyponatremia.

American journal of kidney diseases : the official journal of the National Kidney Foundation, 2008

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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