Can Strattera (atomoxetine) cause hyponatremia (low sodium levels)?

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Last updated: January 15, 2026View editorial policy

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Strattera and Hyponatremia Risk

Strattera (atomoxetine) is not established as a cause of hyponatremia, and routine sodium monitoring is not indicated for patients taking this medication. 1

Evidence Assessment

The available evidence does not support a direct association between atomoxetine and hyponatremia:

  • No established link exists between atomoxetine and hyponatremia based on current guideline recommendations from the American Academy of Pediatrics and other guideline societies 1

  • Routine sodium monitoring is not recommended for patients taking atomoxetine, unlike medications with known hyponatremia risk 1

  • The adverse effect profile of atomoxetine includes nausea, vomiting, fatigue, decreased appetite, abdominal pain, and somnolence—but not hyponatremia 1

Clinical Monitoring Recommendations

Standard monitoring for atomoxetine focuses on:

  • Cardiovascular parameters (heart rate and blood pressure) 1
  • Growth parameters (height and weight) 1
  • Psychiatric symptoms, including suicidal ideation 1
  • Sodium monitoring is not part of routine surveillance 1

If Hyponatremia Develops

When hyponatremia occurs in a patient taking atomoxetine, investigate alternative causes first:

  • Concurrent medications that are known to cause hyponatremia, such as SSRIs, diuretics, or other antidepressants 1
  • Underlying medical conditions including heart failure, cirrhosis, or SIADH from other causes 1
  • Volume status abnormalities (hypovolemic, euvolemic, or hypervolemic states) 1

Diagnostic workup should include:

  • Serum and urine osmolality 1
  • Urine sodium concentration 1
  • Assessment of extracellular fluid volume status 1

Important Distinction from SSRIs

This contrasts sharply with SSRIs like paroxetine, which have well-documented associations with hyponatremia:

  • Paroxetine causes hyponatremia in approximately 12% of older adults 2
  • Mean time to development is 9.3 days after initiation 2
  • The mechanism involves SIADH (syndrome of inappropriate antidiuretic hormone secretion) 3, 4
  • Antidepressants as a class place patients at high risk for hyponatremia 1

Atomoxetine, as a selective norepinephrine reuptake inhibitor rather than an SSRI, does not share this risk profile 5, 6

References

Guideline

Atomoxetine and Hyponatremia Risk

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Hyponatremia associated with paroxetine.

Pharmacopsychiatry, 1998

Research

Clinical pharmacokinetics of atomoxetine.

Clinical pharmacokinetics, 2005

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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