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

Hartmannuv Roztok Viaflo Baxter

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

Hartmannuv Roztok Viaflo Baxter (Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate)

Hartmannuv Roztok Viaflo Baxter is an intravenous electrolyte solution containing potassium chloride, sodium chloride, calcium chloride dihydrate, and sodium lactate. It is supplied as a sterile solution for infusion, formulated to provide balanced electrolytes and fluid volume. Marketed in the European Union, it is used for fluid and electrolyte replacement in patients with hypovolemia, metabolic acidosis, or postoperative fluid loss under medical supervision and appropriate monitoring.

Manufacturer / TM Owner

Baxter Czech Spol. S R.O.

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Indications & Clinical Uses

Hartmannuv Roztok Viaflo Baxter is indicated for clinical situations and that require rapid restoration of extracellular fluid volume and electrolyte balance.

  • Fluid replacement in patients with hypovolemia due to blood loss, dehydration, or burns.
  • Electrolyte replenishment for conditions associated with sodium, potassium, or calcium deficits.
  • Correction of metabolic acidosis by providing lactate which is metabolized to bicarbonate.
  • Support during major surgery or postoperative care to maintain intravascular volume.
  • Use in pediatric or adult patients when balanced electrolyte solutions are required.

Side Effects

The safety profile of Hartmannuv Roztok Viaflo Baxter reflects the typical reactions observed with intravenous electrolyte solutions.

Common

  • Mild vein irritation or pain at the infusion site, usually a brief burning sensation that resolves after the line is removed.
  • Transient nausea or vomiting during or shortly after infusion, typically self‑limiting.
  • Slight increase in serum sodium or potassium that normalizes after therapy, monitored with routine labs.

Serious

  • Hyperkalemia leading to cardiac arrhythmia, which may present as palpitations, dizziness, or serious rhythm disturbances.
  • Hypernatremia causing neurological symptoms such as confusion, lethargy, or seizures, especially in patients with impaired water balance.
  • Severe allergic reaction (anaphylaxis) with rash, swelling, bronchospasm, or hypotension.

Precautions & Warnings

When prescribing Hartmannuv Roztok Viaflo Baxter, clinicians should consider several precautions to ensure safe administration.

  • Assess baseline electrolyte levels and renal function before initiating therapy.
  • Adjust infusion rate in patients at risk of fluid overload, such as those with heart failure or pulmonary edema.
  • Monitor serum potassium and sodium frequently during treatment, especially in patients receiving other electrolyte-modifying drugs.
  • Use caution in neonates, infants, and the elderly due to altered fluid and electrolyte handling.
  • Avoid rapid infusion that may cause hyperosmolar shifts and vascular irritation.
  • Discontinue the solution if signs of allergic reaction or severe electrolyte imbalance develop.

Avoid Interactions

Hartmannuv Roztok Viaflo Baxter may interact with other medications that affect fluid balance, electrolytes, or acid‑base status.

Avoid

  • Concomitant use with high‑dose potassium supplements or potassium‑sparing diuretics, which can precipitate hyperkalemia.
  • Simultaneous administration with hypertonic saline solutions, which may cause excessive sodium load.

Use with caution

  • Co‑administration with ACE inhibitors or ARBs, requiring close monitoring of potassium and renal function.
  • Use together with loop diuretics, as they can alter sodium and calcium balance and necessitate electrolyte checks.
  • Combination with insulin or beta‑agonists, which shift potassium intracellularly and may lead to hypokalemia.

Frequently Asked Questions

The solution contains potassium chloride, sodium chloride, calcium chloride dihydrate, and sodium lactate as its active electrolyte components.

It is used for fluid replacement, electrolyte replenishment, correction of metabolic acidosis, treatment of hypovolemia, and postoperative fluid management.

The product is supplied as a sterile solution for intravenous infusion and is administered through a controlled IV infusion set.

Yes, the solution can be used in pediatric patients when a balanced electrolyte infusion is required, under appropriate medical supervision.

Routine monitoring of serum electrolytes (sodium, potassium, calcium) and renal function is recommended, especially when the patient receives other electrolyte‑affecting medications.

Compatibility should be confirmed with the pharmacy; mixing with other hypertonic solutions may increase sodium load and should be avoided.

The infusion should be stopped immediately, and appropriate medical treatment for anaphylaxis should be initiated according to clinical protocols.

The product is a sterile, preservative‑free solution intended for single‑use administration.

Unopened containers should be stored at controlled room temperature, protected from light, and kept within the temperature range specified on the label.

Sodium lactate acts as a buffer; it is metabolized to bicarbonate, helping to correct metabolic acidosis during infusion.

Yes, it is classified as a prescription‑only product and must be administered under the direction of a qualified healthcare professional.

Patients with renal impairment require careful monitoring of electrolyte levels and may need dose adjustments or alternative therapies.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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