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Hartmann Viaflo

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

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

Hartmann Viaflo is an intravenous electrolyte solution containing potassium chloride, sodium chloride, calcium chloride dihydrate, and sodium lactate. The formulation is supplied as a sterile solution for infusion, with the specific concentration of each ion not publicly disclosed. It is marketed in the European Union and requires a prescription. Viaflo is used to replenish fluid volume and correct electrolyte imbalances in clinical settings for patients.

Manufacturer / TM Owner

Baxter Sa

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Indications & Clinical Uses

Hartmann Viaflo is indicated for intravenous fluid and electrolyte replacement in a variety of clinical situations.

  • Treatment of hypokalemia (low potassium).
  • Management of hyponatremia (low sodium).
  • Correction of calcium deficiency or hypocalcemia.
  • Support of patients requiring fluid resuscitation after surgery or trauma.
  • Use in patients with metabolic acidosis where lactate serves as a buffer.

Side Effects

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

Common

  • Mild infusion site irritation or pain.
  • Transient nausea or vomiting.
  • Slight increase in serum chloride levels.
  • Temporary mild hypernatremia.

Serious

  • Severe hyperkalemia leading to cardiac arrhythmia.
  • Rapid fluid overload causing pulmonary edema.
  • Allergic reaction with rash, urticaria, or anaphylaxis.
  • Metabolic alkalosis from excess lactate conversion.

Precautions & Warnings

When prescribing Hartmann Viaflo, clinicians should evaluate patient-specific factors and monitor relevant laboratory values.

  • Assess baseline electrolyte concentrations, especially potassium, sodium, and calcium.
  • Monitor cardiac rhythm in patients at risk for arrhythmias.
  • Use caution in renal impairment due to reduced electrolyte excretion.
  • Avoid rapid infusion in patients with heart failure or pulmonary edema.
  • Adjust dose in patients receiving diuretics or other electrolyte-modifying drugs.
  • Consider pregnancy status; safety data are limited.

Avoid Interactions

Hartmann Viaflo may interact with other medications that affect electrolyte balance or fluid status.

Avoid

  • Concurrent use of potassium-sparing diuretics or potassium supplements, which can precipitate hyperkalemia.
  • High-dose sodium bicarbonate, which may exacerbate hypernatremia.
  • Calcium channel blockers combined with large calcium loads, increasing risk of hypercalcemia.

Use with caution

  • Loop diuretics, which can cause rapid shifts in potassium and sodium.
  • ACE inhibitors or ARBs, which may alter potassium handling.
  • Insulin therapy, which drives potassium into cells and may require electrolyte monitoring.

Frequently Asked Questions

Hartmann Viaflo is used to replace lost fluids and electrolytes intravenously, helping to correct imbalances such as low potassium, sodium, or calcium.

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

It is given intravenously in hospitals or clinical settings when patients need rapid fluid and electrolyte replenishment, such as after surgery, trauma, or severe dehydration.

Use requires caution; renal impairment can affect electrolyte clearance, so close monitoring of serum levels is recommended.

Clinicians usually monitor vital signs, cardiac rhythm, and serum electrolytes (potassium, sodium, calcium) before and after infusion.

The solution may be used in children under medical supervision, with dosing adjusted for age and weight.

Common side effects include mild infusion site irritation, transient nausea, and temporary changes in serum chloride or sodium levels.

Serious reactions may include hyperkalemia leading to cardiac arrhythmias, fluid overload with pulmonary edema, severe allergic responses, or metabolic alkalosis from excess lactate.

Yes, concurrent potassium supplements can increase the risk of hyperkalemia and should generally be avoided.

Sodium lactate acts as a buffer that can be metabolized to bicarbonate, helping to correct metabolic acidosis.

Safety data are limited; the solution should be used only if the potential benefit justifies any potential risk to the fetus.

Infusion should be stopped immediately, and appropriate medical treatment for an allergic reaction, such as antihistamines or epinephrine, should be administered.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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