Product image of Hartmann Viaflo Baxter (Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate) supplied by GNH India

Hartmann Viaflo Baxter

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

Hartmann Viaflo Baxter (Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate)

Hartmann Viaflo Baxter is an intravenous solution containing potassium chloride, sodium chloride, calcium chloride dihydrate, and sodium lactate. It is supplied as a sterile fluid for infusion, marketed in the European Union, and classified as a prescription‑only IV electrolyte solution used to replace fluid and electrolytes. It provides essential ions to help maintain extracellular fluid volume and acid‑base balance during surgery, trauma, or medical conditions that cause dehydration.

Manufacturer / TM Owner

Baxter Sa

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Indications & Clinical Uses

Hartmann Viaflo Baxter is indicated for clinical situations where fluid and electrolyte replacement is required.

  • Restoration of extracellular fluid volume after blood loss or dehydration.
  • Replenishment of potassium, sodium, calcium, and lactate ions in patients with electrolyte deficits.
  • Maintenance of plasma volume during major surgery or intensive care.
  • Treatment of metabolic acidosis by providing lactate that is metabolized to bicarbonate.
  • Support for patients receiving parenteral nutrition who need additional electrolytes.

Side Effects

Adverse reactions to Hartmann Viaflo Baxter are generally infrequent, but they can be categorized by frequency and severity.

Common

  • Mild pain or irritation at the infusion site.
  • Transient increase in serum potassium or calcium levels.
  • Slight nausea or vomiting.
  • Low-grade fever.

Serious

  • Hyperkalemia leading to cardiac arrhythmia.
  • Hypercalcemia causing muscle weakness or confusion.
  • Fluid overload with pulmonary edema.
  • Severe allergic reaction such as anaphylaxis.

Precautions & Warnings

When using Hartmann Viaflo Baxter, clinicians should consider several precautions to minimize risk and ensure appropriate therapy.

  • Assess baseline electrolyte concentrations and renal function before initiation.
  • Adjust infusion rate in patients with heart failure or compromised pulmonary status.
  • Monitor serum potassium and calcium levels during and after administration.
  • Use caution in patients with metabolic alkalosis, as lactate conversion may affect acid‑base balance.
  • Avoid rapid infusion in neonates or patients with fragile veins.
  • Consider compatibility with other IV medications; incompatibility may cause precipitation.

Avoid Interactions

Hartmann Viaflo Baxter may interact with other drugs administered intravenously or orally; awareness of these interactions helps prevent complications.

Avoid

  • Concurrent administration of potassium‑sparing diuretics or ACE inhibitors that may increase serum potassium.
  • Calcium‑containing solutions given through the same line, which can precipitate calcium phosphate.
  • High‑dose sodium bicarbonate, which may exacerbate fluid overload.

Use with caution

  • Loop diuretics, as they can cause rapid shifts in electrolytes.
  • Blood products, requiring monitoring of electrolyte balance.
  • Medications that affect cardiac conduction (e.g., digoxin) when hyperkalemia is possible.

Frequently Asked Questions

It is used to replace lost fluids and electrolytes, maintain plasma volume, and correct electrolyte imbalances in various clinical settings.

Unlike normal saline, Hartmann Viaflo Baxter contains potassium, calcium, and lactate in addition to sodium and chloride, providing a more balanced electrolyte composition.

The solution includes potassium chloride, sodium chloride, calcium chloride dihydrate, and sodium lactate.

It is commonly given during surgery, trauma resuscitation, intensive care, and when patients require parenteral nutrition or have electrolyte deficiencies.

Clinicians should monitor vital signs, fluid balance, and serum levels of potassium, calcium, and sodium throughout the infusion.

Use in children should be based on careful assessment of electrolyte needs and dosing calculations performed by a qualified healthcare professional.

Symptoms may include rash, itching, swelling, difficulty breathing, or anaphylaxis, and require immediate medical attention.

Lactate is metabolized to bicarbonate in the liver, helping to correct metabolic acidosis.

Compatibility varies; it should be checked for each medication, as some drugs may precipitate when mixed with calcium or potassium.

Contraindications include known hypersensitivity to any component and conditions where fluid overload or hyperkalemia would be hazardous.

Store at controlled room temperature, protected from light, and keep the container sealed until use.

The ATC classification for this product is B05AA03.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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