Product image of Gluconate De Calcium B.Braun (Calcium Gluconate) supplied by GNH India

Gluconate De Calcium B.Braun

Active Ingredient:
Calcium Gluconate
Origin:
EU

Gluconate De Calcium B.Braun (Calcium Gluconate)

Calcium gluconate B.Braun is a calcium gluconate preparation supplied by B. Braun. It is a prescription‑only product marketed in the European Union. The formulation is intended for parenteral administration, available for intramuscular and intravenous injection. While the exact strength and dosage form are not specified in the label, the active ingredient provides calcium ions for physiological needs. It is classified as a calcium supplement and electrolyte replacement.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Calcium gluconate B.Braun is used to address conditions related to low calcium levels and to support specific electrolyte management in clinical practice.

  • Treatment of hypocalcemia resulting from surgery, trauma, or endocrine disorders.
  • Management of calcium deficiency in patients receiving parenteral nutrition.
  • Adjunct therapy for hyperkalemia to protect cardiac membranes.
  • Counteracting magnesium toxicity by providing calcium ions.
  • Prevention of tetany in patients with impaired parathyroid function.
  • Support of bone mineralization during acute care when oral calcium is not feasible.

Side Effects

Adverse reactions to calcium gluconate B.Braun are generally infrequent, but they can be categorized by frequency and clinical significance.

Common

  • Mild pain, redness, or swelling at the injection site.
  • Transient nausea or vomiting.
  • Temporary feeling of warmth or flushing.
  • Headache or dizziness shortly after administration.

Serious

  • Severe hypercalcemia with symptoms such as confusion, muscle weakness, or cardiac arrhythmia.
  • Allergic reactions including rash, itching, bronchospasm, or anaphylaxis.
  • Extravasation causing tissue necrosis if the solution leaks into surrounding tissue.
  • Rapid drop in blood pressure (hypotension) especially with rapid IV infusion.

Precautions & Warnings

When administering calcium gluconate B.Braun, clinicians should observe several precautionary measures to minimize risk and ensure therapeutic effectiveness.

  • Verify serum calcium levels before and after infusion to avoid over‑correction.
  • Use a controlled infusion rate; rapid IV administration can provoke cardiac disturbances.
  • Assess for a history of hypersensitivity to calcium salts or excipients.
  • Monitor cardiac rhythm continuously during intravenous delivery, especially in patients with underlying heart disease.
  • Avoid use in patients with severe hypercalcemia unless specifically indicated.
  • Ensure proper catheter placement to prevent extravasation and tissue injury.
  • Adjust dose in renal impairment, as calcium clearance may be reduced.

Avoid Interactions

Calcium gluconate can interact with various medications; awareness of these interactions helps prevent adverse outcomes.

Avoid

  • Concomitant use with bisphosphonates administered intravenously, which may cause acute hypocalcemia.
  • Simultaneous infusion with high‑dose loop diuretics that increase calcium excretion.

Use with caution

  • Calcium channel blockers may enhance calcium’s effect on cardiac conduction; monitor ECG.
  • Digoxin therapy can be potentiated by calcium, increasing risk of toxicity.
  • Iron or zinc supplements may reduce calcium absorption; separate administration times.
  • Antacids containing aluminum or magnesium can alter calcium balance; observe serum levels.

Frequently Asked Questions

The primary indication is the treatment of hypocalcemia, a condition characterized by low serum calcium levels.

Yes, it is commonly administered to address calcium deficiency in patients who are receiving total parenteral nutrition.

Calcium gluconate acts as a protective agent for cardiac membranes, reducing the risk of arrhythmias associated with elevated potassium levels.

It can be used as part of the management of magnesium toxicity because calcium ions antagonize the effects of excess magnesium.

The product is formulated for parenteral use and may be administered either intramuscularly or intravenously, depending on clinical need.

Continuous cardiac monitoring and frequent checks of serum calcium levels are advised to detect rapid changes or arrhythmias.

The product should be stored at controlled room temperature, protected from light, and kept in the original container until use.

Dose adjustments may be necessary in renal impairment because reduced clearance can increase the risk of hypercalcemia.

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

Intravenous infusion should be performed slowly to avoid cardiac disturbances; rapid administration is associated with higher risk of adverse events.

Compatibility should be verified with each co‑administered solution; incompatibility can lead to precipitation or reduced efficacy.

The ATC classification for calcium gluconate is A12AA04.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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