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Gluconat De Calciu Hameln

Active Ingredient:
Calcium Gluconate For Injection
Origin:
EU

Gluconat De Calciu Hameln (Calcium Gluconate For Injection)

Gluconat De Calciu Hameln is a calcium gluconate injection solution supplied in a sterile aqueous form for intravenous administration. The product contains calcium gluconate as the active ingredient; the specific concentration is not disclosed in the summary. It is marketed in the European Union and is available only by prescription. The formulation is intended to provide a readily bioavailable source of calcium ions for clinical use.

Manufacturer / TM Owner

Hameln Pharma Gmbh

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Indications & Clinical Uses

Gluconat De Calciu Hameln is indicated for several clinical situations where calcium supplementation is required.

  • Treatment of hypocalcemia resulting from surgical, traumatic, or metabolic causes.
  • Support of calcium levels during parenteral nutrition.
  • Cardiac membrane stabilization in patients with hyperkalemia undergoing emergency therapy.
  • Management of calcium deficiency associated with vitamin D deficiency or renal disease.
  • Adjunct therapy for magnesium toxicity to counteract neuromuscular excitability.

Side Effects

Adverse reactions to calcium gluconate injection are generally infrequent, but they can be categorized by frequency and severity.

Common

  • Local irritation or pain at the injection site.
  • Mild nausea or vomiting.
  • Transient flushing or warmth sensation.
  • Mild hypotension when administered rapidly.

Serious

  • Severe hypercalcemia with cardiac arrhythmias.
  • Tissue necrosis if extravasation occurs.
  • Allergic reactions such as urticaria, bronchospasm, or anaphylaxis.

Precautions & Warnings

Before administering Gluconat De Calciu Hameln, clinicians should consider several precautionary measures to minimize risk.

  • Verify serum calcium levels; avoid use in patients with documented hypercalcemia.
  • Use a controlled infusion rate to prevent rapid shifts in calcium concentration.
  • Monitor cardiac rhythm and blood pressure during and after infusion.
  • Assess for signs of extravasation; discontinue infusion if tissue damage is suspected.
  • Use with caution in patients with renal impairment or active kidney stones.
  • Pregnancy and lactation status should be evaluated, as safety data are limited.

Avoid Interactions

Calcium gluconate may interact with other medications, influencing their efficacy or safety.

Avoid

  • Loop diuretics (e.g., furosemide) that increase calcium excretion.
  • Bisphosphonates administered concurrently, which can reduce calcium absorption.
  • Calcium‑containing antacids or oral supplements that may cause hypercalcemia.

Use with caution

  • Digoxin, as calcium levels can affect its therapeutic window.
  • Cardiac glycosides and other drugs that prolong the QT interval.
  • Magnesium sulfate, because calcium may counteract its effects.

Frequently Asked Questions

The primary indication is the treatment of hypocalcemia, especially when rapid correction of serum calcium is required.

It is administered intravenously, typically as a controlled infusion under medical supervision.

Use with caution; renal impairment can affect calcium balance, so serum calcium should be closely monitored.

Continuous cardiac monitoring, blood pressure checks, and periodic serum calcium measurements are recommended.

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

The infusion should be stopped immediately, the area should be elevated, and appropriate measures to prevent tissue injury should be taken.

Yes, calcium levels can influence digoxin’s therapeutic window, so serum levels of both agents should be monitored.

Calcium stabilizes cardiac membranes, reducing the risk of arrhythmias associated with high potassium levels.

Common side effects include local irritation, mild nausea, flushing, and transient hypotension.

Calcium antagonizes the neuromuscular effects of excess magnesium, helping to restore normal muscle function.

Dose adjustments may be necessary based on renal function and baseline calcium levels, which can be altered in older adults.

Serum calcium, magnesium, potassium, renal function, and ECG are typically evaluated prior to initiation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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