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1 May 2026Oral drugsSource update: February 2024

Potassium Chloride Immediate-Release Oral: Dosing

Immediate-release potassium chloride guidance for moderate hypokalaemia when a rapid oral effect is required.

Also searched as

Potassium chloride immediate-releasePotassium chloride syrup
Prescription under medical supervision

Source reviewed

February 2024

Guide category

Oral drugs

Safety boundary

Prescription medicine information for clinician-guided use.

Kenza Health Hub presents this medicine page as structured health education. Check dose, route, interactions, pregnancy or breast-feeding considerations, and local protocol with a qualified clinician or pharmacist. Read our medical editorial policy.

This guide page is for structured reference only and does not replace a clinician, pharmacist, or emergency review. Dose choice, route choice, interactions, and safety decisions still need professional judgment.

Therapeutic action

Potassium supplement, when immediate effect is required.

Indications

Treatment of moderate hypokalaemia.

Forms and strengths

  • 7.5% potassium chloride syrup providing 1 mmol of potassium per ml, to be administered using a measuring device.

Dose

  • Child under 45 kg: 2 mmol/kg, corresponding to 2 ml/kg, daily.
  • Child 45 kg and over and adult: 30 mmol, corresponding to 30 ml, 3 times daily.
Potassium chloride syrup dose by age and weight
AgeWeight7.5% syrup
< 2 months< 5 kg4 ml x 2
2 months to < 1 year5 to < 10 kg6 ml x 2
1 to < 3 years10 to < 15 kg12 ml x 2
3 to < 5 years15 to < 20 kg20 ml x 2
5 to < 7 years20 to < 25 kg25 ml x 2
7 to < 9 years25 to < 30 kg20 ml x 3
9 to < 13 years30 to < 45 kg25 ml x 3
≥ 13 years and adult≥ 45 kg30 ml x 3

Duration

According to clinical response. Treatment of 1 to 2 days is typically sufficient when the patient is fully able to drink oral rehydration solution and can eat.

Contra-indications, adverse effects, precautions

  • Reduce dosage in older patients and patients with renal impairment because of the risk of hyperkalaemia.
  • Do not combine with spironolactone and angiotensin-converting-enzyme inhibitors such as enalapril.
  • May cause gastrointestinal ulcerations, diarrhoea, nausea, vomiting, and rarely hyperkalaemia.
  • Administer with caution to patients with gastrointestinal ulcer because of the risk of gastrointestinal ulcerations.
  • Pregnancy: no contra-indication.
  • Breast-feeding: no contra-indication.
  • Take with or at the end of meals to reduce the risk of gastrointestinal ulcerations.

Source

MSF Essential drugs practical guidelines (January 2026)

This page combines source-derived medicine reference sections with Kenza editorial context, while leaving out the Storage and Remarks sections from the source batch.

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