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 pharmaceutical solution presented as an intravenous preparation for infusion use. It is employed to manage phosphate balance in clinical settings.
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 phosphate supplementation for conditions where phosphate balance is disrupted.

  • Hypophosphatemia: restores serum phosphate levels in patients with low phosphate.
  • Renal replacement therapy: supplies phosphate during dialysis to maintain electrolyte homeostasis.
  • Metabolic acidosis correction: contributes buffering capacity to assist in pH regulation during critical care.

How It Works

  • The buffered phosphate solution delivers inorganic phosphate ions that participate in cellular energy metabolism, nucleic acid synthesis, and acid‑base buffering. Intravenous administration rapidly increases extracellular phosphate, supporting ATP production and helping to correct acid‑base disturbances by acting as a physiological buffer.

Side Effects

Nephromag may be associated with a range of adverse reactions.

Common Side Effects

  • Hyperphosphatemia: elevated serum phosphate levels.
  • Hypocalcemia: reduced calcium concentrations secondary to phosphate binding.
  • Infusion site irritation: redness or discomfort at the injection site.
  • Nausea: mild gastrointestinal upset.
  • Headache: transient cranial discomfort.
  • Flushing: temporary warmth or redness of the skin.

Serious or Rare Side Effects

  • Metastatic calcification: calcium‑phosphate deposition in soft tissues.
  • Cardiac arrhythmia: rhythm disturbances linked to electrolyte shifts.
  • Severe allergic reaction: anaphylaxis or hypersensitivity.
  • Renal failure exacerbation: worsening kidney function in susceptible patients.
  • Hemodynamic instability: sudden blood pressure changes during infusion.
  • Seizures: neurologic events related to electrolyte imbalance.

Precautions & Warnings

Nephromag should be used with careful clinical monitoring.

  • Serum phosphate monitoring: check levels before and during therapy.
  • Calcium balance: assess calcium status to avoid hypocalcemia.
  • Renal function assessment: evaluate kidney performance prior to infusion.
  • Hyperphosphatemia avoidance: do not administer to patients with already high phosphate.
  • Infusion rate control: administer slowly to reduce risk of cardiovascular effects.
  • 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 electrolyte balance.

Major Interactions (Avoid)

  • Calcium supplements: may precipitate calcium‑phosphate complexes.
  • Antacids containing aluminum or magnesium: can interfere with phosphate absorption.
  • Vitamin D analogues: potentiate hyperphosphatemia risk.

Moderate Interactions (Monitor Closely)

  • Loop diuretics: increase renal phosphate loss, requiring dose adjustment.
  • ACE inhibitors: may affect renal handling of phosphate.
  • Bisphosphonates: combined effect on bone mineral metabolism.
  • Parathyroid hormone analogues: alter calcium‑phosphate dynamics.

Frequently Asked Questions

Nephromag is an intravenous buffered phosphate solution used to correct low phosphate levels, support electrolyte balance during renal replacement therapy, and assist in managing metabolic acidosis in acute care settings.

The solution provides inorganic phosphate ions that quickly raise serum phosphate, participate in ATP synthesis, and act as a physiological buffer to help stabilize blood pH during critical illness.

The dosage of Nephromag is determined by the prescribing clinician based on the patient’s serum phosphate, renal function, and overall clinical condition. No fixed regimen is provided here.

Safety data for Nephromag in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible 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, 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 (including cold‑chain if needed), and import documentation.

Nephromag offers a buffered formulation that may provide more stable pH control compared with non‑buffered phosphate salts. Its intravenous route allows rapid correction of phosphate deficits, which can be advantageous over oral preparations in critically ill patients.

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

Nephromag is administered intravenously, typically via a controlled infusion. The exact rate and duration are set by the treating physician according to the patient’s clinical needs and laboratory values.

Serious risks include hyperphosphatemia leading to metastatic calcification, severe hypocalcemia, cardiac arrhythmias, and rare anaphylactic reactions. Continuous monitoring of electrolytes and cardiac status is essential during therapy.

Nephromag should be avoided in patients with existing hyperphosphatemia, uncontrolled calcium disorders, severe renal failure not managed by dialysis, or known hypersensitivity to any component of the formulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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