Product image of Hylvastam (Sodium Hydrogen Carbonate) supplied by GNH India

Hylvastam

Active Ingredient:
Sodium Hydrogen Carbonate
Origin:
EU

Hylvastam (Sodium Hydrogen Carbonate)

Sodium Hydrogen Carbonate, the active ingredient in Hylvastam, is an excipient presented as an intravenous solution for use as a buffering agent in parenteral preparations. It helps maintain pH balance in intravenous fluids and related pharmaceutical formulations.

GNH India supplies Hylvastam as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and clinics worldwide, adhering to EU quality standards and providing reliable global distribution. The product is manufactured under GMP conditions and is available for bulk and unit‑dose requirements.

Manufacturer / TM Owner

Macure Pharma Aps

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Indications & Clinical Uses

Hylvastam is used as an excipient to manage pH and stability in various intravenous and parenteral applications.

  • Buffering in intravenous admixtures: helps maintain pH stability of IV solutions.
  • pH adjustment in parenteral nutrition: provides appropriate alkalinity for nutrient compatibility.
  • Stabilizer in vaccine formulations: supports antigen integrity during storage and administration.

How It Works

  • Sodium Hydrogen Carbonate dissociates in aqueous solution to release bicarbonate ions, which act as a physiological buffer. The bicarbonate system buffers hydrogen ions, thereby raising or stabilizing the pH of intravenous fluids. This buffering capacity helps maintain the desired acidity/alkalinity of parenteral preparations, ensuring chemical stability and compatibility with other components.

Side Effects

Adverse reactions may occur when sodium hydrogen carbonate is administered intravenously.

Common Side Effects

  • Metabolic alkalosis: elevation of blood pH.
  • Hypernatremia: increased serum sodium levels.
  • Fluid overload: excess extracellular fluid volume.
  • Hypokalemia: reduced serum potassium.
  • Local irritation at infusion site.
  • Transient hypertension.

Serious or Rare Side Effects

  • Severe alkalosis leading to seizures.
  • Cardiac arrhythmias, especially in patients with underlying heart disease.
  • Pulmonary edema due to fluid shifts.
  • Hypocalcemia causing tetany.
  • Acute renal failure in susceptible individuals.
  • Anaphylactic reaction to excipient components.

Precautions & Warnings

When using Hylvastam, consider the following safety measures.

  • Dose adjustment: monitor serum electrolytes and acid‑base status.
  • Renal function: assess kidney function before administration.
  • Cardiac status: observe for arrhythmias in patients with heart disease.
  • Acid‑base balance: avoid use in patients with existing metabolic alkalosis.
  • Allergy: discontinue if hypersensitivity or anaphylaxis occurs.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Potential drug interactions should be reviewed prior to administration.

Major Interactions (Avoid)

  • Concurrent calcium‑containing solutions: risk of precipitation.
  • Co‑administration with other alkalinizing agents: may cause excessive alkalosis.
  • Use with loop diuretics: can increase sodium load and affect electrolyte balance.

Moderate Interactions (Monitor Closely)

  • Antihypertensive medications: monitor blood pressure for additive effects.
  • Nephrotoxic drugs: observe renal function closely.
  • Insulin therapy: watch for shifts in potassium levels.
  • Anticoagulants: assess for changes in plasma pH that may affect drug activity.

Frequently Asked Questions

Hylvastam is an excipient containing sodium hydrogen carbonate that is used to buffer and stabilize the pH of intravenous and parenteral solutions, such as admixtures, nutrition formulations, and vaccine preparations.

Sodium hydrogen carbonate dissociates to release bicarbonate ions, which act as a physiological buffer. The bicarbonate system neutralizes excess hydrogen ions, thereby maintaining or raising the pH of the solution to the desired level.

The dose of Hylvastam is determined by the prescribing clinician based on the specific formulation, required pH adjustment, and patient factors. No fixed regimen is provided publicly.

Safety data for sodium hydrogen carbonate as an excipient in pregnancy or lactation are limited. Use should be considered only if clearly needed and after risk‑benefit assessment by the healthcare professional.

To order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Compared with alternatives such as acetate or phosphate buffers, sodium hydrogen carbonate offers rapid pH adjustment and is physiologically compatible with most intravenous formulations, but it may increase sodium load and requires careful electrolyte monitoring.

Store Hylvastam at ambient temperature, below 25 °C, in its original packaging. Protect it from moisture, direct sunlight, and extreme temperature fluctuations to maintain its stability.

Hylvastam is supplied as an injectable solution for intravenous use. It is added to the IV bag or infusion set under aseptic conditions according to the prescribed concentration and volume.

Serious risks include severe metabolic alkalosis, cardiac arrhythmias, pulmonary edema, and anaphylactic reactions. Monitoring of electrolytes, acid‑base status, and patient tolerance is essential during administration.

Patients with known hypersensitivity to sodium hydrogen carbonate, uncontrolled metabolic alkalosis, severe renal impairment, or those at high risk for fluid overload should avoid using Hylvastam unless specifically directed by a qualified clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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