Product image of Hartmann’s Solution Compound Sodium Lactate Laboratoire Aguettant (Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate) supplied by GNH India

Hartmann’s Solution Compound Sodium Lactate Laboratoire Aguettant

Active Ingredient:
Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate
Origin:
EU

Hartmann’s Solution Compound Sodium Lactate Laboratoire Aguettant (Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate)

Hartmann’s Solution Compound Sodium Lactate Laboratoire Aguettant is an intravenous electrolyte solution containing potassium chloride, sodium chloride, calcium chloride dihydrate, and sodium lactate. It is supplied as a sterile liquid for infusion, without a specified concentration, and is marketed in the European Union as a prescription‑only product. The formulation is designed to replace extracellular fluid, provide essential electrolytes, and assist in correcting metabolic acidosis in clinical practice.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Hartmann’s solution is indicated for several clinical situations that require rapid restoration of intravascular volume and electrolyte balance.

  • Fluid resuscitation in patients with hypovolemia due to trauma, surgery, or dehydration.
  • Electrolyte replacement when sodium, potassium, or calcium deficits are identified.
  • Correction of metabolic acidosis, particularly in postoperative or critically ill patients.
  • Maintenance of fluid and electrolyte homeostasis during major operative procedures.
  • Supportive therapy for patients receiving large volumes of blood products or diuretics.
  • Prevention of electrolyte shifts during rapid infusion of crystalloids in intensive‑care settings.

Side Effects

Adverse reactions to Hartmann’s solution are generally related to its electrolyte composition and the intravenous route of administration.

Common

  • Mild hypernatremia or hyponatremia depending on infusion rate.
  • Transient potassium or calcium level fluctuations.
  • Local irritation or pain at the infusion site.
  • Mild metabolic alkalosis due to lactate metabolism.
  • Mild increase in serum lactate that resolves after metabolism.
  • Transient changes in blood pH due to lactate conversion.

Serious

  • Severe hyperkalemia leading to cardiac arrhythmia.
  • Hypercalcemia with potential renal impairment.
  • Volume overload causing pulmonary edema.
  • Severe metabolic acidosis if administered inappropriately.
  • Anaphylactoid reactions such as urticaria, hypotension, or bronchospasm.
  • Severe electrolyte imbalance leading to neuromuscular dysfunction.

Precautions & Warnings

When prescribing Hartmann’s solution, clinicians should evaluate patient-specific factors and monitor parameters to minimize risks associated with electrolyte and volume shifts.

  • Assess baseline serum electrolytes, renal function, and acid‑base status before initiation.
  • Adjust infusion rate in patients with cardiac or renal insufficiency to avoid volume overload.
  • Use caution in individuals with hyperkalemia, hypercalcemia, or severe metabolic acidosis.
  • Monitor blood pressure, central venous pressure, and urine output during therapy.
  • Re‑evaluate electrolyte levels and arterial blood gases regularly, especially after large volumes.
  • Avoid rapid administration in neonates or patients with compromised vascular integrity.

Avoid Interactions

Hartmann’s solution may interact with other intravenous or oral agents that affect electrolyte balance, cardiac conduction, or fluid status.

Avoid

  • Concurrent infusion of high‑dose potassium chloride solutions, which can precipitate severe hyperkalemia.
  • Administration with calcium‑containing medications when rapid infusion rates are used, increasing risk of calcium overload.
  • Use with sodium bicarbonate in large volumes, which may exacerbate metabolic alkalosis.

Use with caution

  • Loop diuretics, as they can amplify electrolyte shifts; monitor serum levels closely.
  • ACE inhibitors or ARBs, which may affect potassium handling; adjust monitoring frequency.
  • Blood products, especially packed red cells, because combined volume may lead to overload.

Frequently Asked Questions

Hartmann’s solution is used to restore extracellular fluid volume, replace key electrolytes, and correct metabolic acidosis in patients who need rapid fluid resuscitation.

The solution contains sodium, potassium, calcium, and lactate, which is metabolized to bicarbonate.

It may be used in children under careful monitoring, but rapid infusion is generally avoided in neonates and infants due to vascular fragility.

Lactate in the solution is metabolized to bicarbonate, which buffers excess hydrogen ions and raises blood pH toward normal levels.

Regular checks of blood pressure, central venous pressure, urine output, serum electrolytes, and arterial blood gases are advised.

It can be used, but infusion rates should be reduced and electrolyte levels closely monitored to avoid volume overload and hyperkalemia.

Rapid infusion can cause electrolyte disturbances, volume overload, pulmonary edema, and local vein irritation.

Unlike normal saline, Hartmann’s solution includes potassium, calcium, and lactate, providing a more balanced electrolyte profile.

Mixing is generally discouraged; compatibility should be confirmed, especially with other electrolyte‑containing solutions.

The infusion should be slowed or stopped, and potassium levels should be re‑checked; alternative fluids without potassium may be considered.

No, it is a prescription‑only medication in the European Union.

The ATC code for Hartmann’s solution is B05AA02, classifying it as a volume expander.

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GNH India Pharmaceuticals Limited

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Last updated:

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