How many milliequivalents (mEq) of potassium are in 1 ampule of potassium phosphate?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: September 2, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Potassium Content in 1 Ampule of Potassium Phosphate

One ampule of potassium phosphate contains 22 mEq of potassium in a 5 mL vial (4.4 mEq/mL) as indicated by the FDA drug label. 1

Potassium Phosphate Composition

Potassium phosphate injection is a concentrated solution containing a mixture of monobasic potassium phosphate and dibasic potassium phosphate in water for injection. The specific composition per the FDA label is:

  • Each 5 mL ampule (single-dose vial) contains:

    • Phosphorus: 15 mmol (3 mmol/mL)
    • Potassium: 22 mEq (4.4 mEq/mL) 1
  • Each 15 mL vial contains:

    • Phosphorus: 45 mmol (3 mmol/mL)
    • Potassium: 66 mEq (4.4 mEq/mL) 1

Clinical Considerations for Administration

Important Warnings

  • Potassium phosphate MUST BE DILUTED before administration
  • Never administer as an undiluted bolus or rapid IV push due to risk of serious cardiac adverse reactions 1
  • Monitor for hyperkalemia, especially in patients with renal impairment
  • Monitor for hyperphosphatemia and resulting hypocalcemia

Dosing Considerations

  • When needed for phosphate replacement in DKA, 20–30 mEq/L potassium phosphate can be added to replacement fluids 2
  • For hypophosphatemia treatment in critically ill patients:
    • Mild-moderate hypophosphatemia: 15 mmol phosphate (22 mEq potassium) has been shown to be effective and safe 3
    • Severe hypophosphatemia: 30 mmol phosphate (44 mEq potassium) may be required 3

Contraindications

  • Severe renal impairment (eGFR less than 30 mL/min/1.73 m²) or end-stage renal disease 1
  • Hyperkalemia
  • Severe hyperphosphatemia

Monitoring Parameters

  • Serum potassium, phosphorus, calcium, and magnesium concentrations should be monitored during therapy
  • ECG monitoring is recommended during administration of high doses or in patients with cardiac conditions
  • More frequent monitoring is required for patients with:
    • Moderate renal impairment
    • Cardiac comorbidities
    • Concomitant medications affecting potassium levels 4

Potential Adverse Effects

  • Hyperkalemia: cardiac conduction disturbances, arrhythmias, hypotension
  • Hyperphosphatemia: hypocalcemia, tissue calcification
  • Vein damage and thrombosis with peripheral administration
  • Aluminum toxicity with prolonged use, especially in patients with renal impairment 1

Clinical Pearls

  • Potassium phosphate is often used when both potassium and phosphate replacement are needed
  • For patients requiring phosphate without additional potassium, sodium phosphate formulations may be preferred
  • Redevelopment of hypophosphatemia is common (45-60% of cases) within 2 days of initial correction, requiring ongoing monitoring and potential additional supplementation 3
  • Phosphate replacement may sometimes be indicated in patients with cardiac dysfunction, anemia, or respiratory depression and in those with serum phosphate concentration <1.0 mg/dl 2

Remember that potassium phosphate is a concentrated electrolyte solution that requires careful administration, appropriate dilution, and monitoring to prevent potentially serious adverse effects.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Hypokalemia Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.