Product image of Nephromag (Buffered Phosphate Solution | Mertiatide) supplied by GNH India

Nephromag

Active Ingredient:
Buffered Phosphate Solution | Mertiatide
Origin:
EU

Nephromag (Buffered Phosphate Solution | Mertiatide)

Buffered Phosphate Solution, the active ingredient in Nephromag, is a phosphate replacement solution presented as a sterile intravenous solution for infusion use. It is employed to correct phosphate deficiency in patients with renal impairment, those undergoing dialysis, or individuals at risk of hypophosphatemia.
GNH India supplies Nephromag as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and transplant centres worldwide.

Manufacturer / TM Owner

Rotop Pharmaka Gmbh

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Indications & Clinical Uses

Nephromag provides intravenous phosphate repletion for conditions affecting phosphate balance.

  • Hypophosphatemia: restores serum phosphate levels in patients with low phosphate.
  • Renal dialysis: supplies phosphate in dialysis fluid to maintain electrolyte homeostasis.
  • Peri‑operative care: delivers phosphate during major surgery to prevent metabolic disturbances.

How It Works

  • Buffered Phosphate Solution delivers inorganic phosphate ions directly into the bloodstream, where they participate in cellular energy metabolism, bone mineralization, and acid‑base buffering. The formulation maintains a physiologic pH, allowing rapid correction of serum phosphate without causing significant shifts in calcium or acid‑base status.

Side Effects

Nephromag may be associated with a range of infusion‑related reactions.

Common Side Effects

  • Hyperphosphatemia: elevated serum phosphate levels.
  • Infusion site pain or erythema.
  • Nausea or vomiting.
  • Mild hypotension during rapid administration.
  • Transient calcium reduction.
  • Electrolyte imbalance (e.g., potassium shift).

Serious or Rare Side Effects

  • Severe hyperphosphatemia leading to calcium‑phosphate precipitation.
  • Anaphylactic or severe allergic reaction.
  • Cardiac arrhythmias secondary to electrolyte disturbances.
  • Metabolic acidosis in susceptible patients.

Precautions & Warnings

Nephromag requires careful monitoring and patient assessment before and during therapy.

  • Serum phosphate monitoring: check levels before infusion and periodically thereafter.
  • Calcium balance: assess calcium levels to avoid precipitation risk.
  • Renal function: evaluate kidney function, especially in patients with chronic kidney disease.
  • Contraindications: avoid in patients with known hyperphosphatemia or severe hypercalcemia.
  • Infusion rate: administer at the rate recommended by the prescriber to reduce infusion reactions.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Nephromag can interact with other agents that affect calcium or phosphate metabolism.

Major Interactions (Avoid)

  • Calcium‑containing IV solutions: risk of calcium‑phosphate precipitation.
  • Vitamin D analogues: may exacerbate hypercalcemia.
  • Aluminum‑containing antacids: reduce phosphate absorption.

Moderate Interactions (Monitor Closely)

  • Loop diuretics: may increase calcium excretion.
  • ACE inhibitors or ARBs: monitor renal function and electrolytes.
  • Parathyroid hormone analogues: adjust phosphate dosing as needed.

Frequently Asked Questions

Nephromag is an intravenous buffered phosphate solution used to correct low phosphate levels in patients with hypophosphatemia, to provide phosphate during renal dialysis, and to support electrolyte balance in peri‑operative or critically ill settings.

The solution delivers inorganic phosphate directly into the bloodstream, where it participates in energy production, bone mineralization, and acid‑base buffering, helping to restore normal serum phosphate concentrations.

The prescribed dose of Nephromag is determined by the treating physician based on the patient’s serum phosphate level, renal function, and clinical condition. Dosing is individualized and should follow the prescriber’s instructions.

Safety of Nephromag in pregnancy or while breastfeeding has not been fully established. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To order Nephromag, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed), and import documentation.

Nephromag provides a buffered formulation that helps maintain physiological pH during infusion, potentially reducing the risk of local irritation compared with non‑buffered phosphate salts. Choice of product depends on clinical setting, compatibility with other IV fluids, and institutional protocols.

Nephromag should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the solution in its original packaging until use to maintain sterility and stability.

Nephromag is administered intravenously, typically as an infusion under the supervision of a healthcare professional. The infusion rate and volume are set by the prescriber and should be monitored for any adverse reactions.

Serious risks include severe hyperphosphatemia leading to calcium‑phosphate precipitation, anaphylactic reactions, and cardiac arrhythmias caused by electrolyte disturbances. Patients should be closely monitored for these events during and after infusion.

Nephromag should be avoided in patients with known hyperphosphatemia, severe hypercalcemia, or a history of hypersensitivity to phosphate solutions. Caution is also advised for individuals with compromised renal function where phosphate accumulation could occur.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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