Product image of Metagelan (Metamizole Sodium Monohydrate) supplied by GNH India

Metagelan

Active Ingredient:
Metamizole Sodium Monohydrate
Origin:
EU

Metagelan (Metamizole Sodium Monohydrate)

Metamizole Sodium Monohydrate, the active ingredient in Metagelan, is a pyrazolone analgesic presented as an oral dosage form for oral use. It provides analgesic and antipyretic effects for the treatment of pain and fever in adults.

GNH India supplies Metagelan as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

G.L. Pharma Gmbh

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Indications & Clinical Uses

Metamizole Sodium Monohydrate is employed for pain and fever management by inhibiting prostaglandin synthesis pathways.

  • Pain: reduces moderate to severe acute pain.
  • Fever: lowers elevated body temperature in febrile states.
  • Postoperative pain: alleviates discomfort following surgical procedures.
  • Colic: eases visceral pain associated with gastrointestinal colic.

How It Works

  • Metamizole Sodium Monohydrate acts as a non‑selective cyclo‑oxygenase (COX) inhibitor, decreasing prostaglandin production throughout the body. In addition, it exerts central analgesic activity by modulating spinal and supraspinal pain pathways, contributing to its antipyretic and analgesic properties.

Side Effects

Metagelan may cause a range of adverse reactions, most of which are dose‑related and reversible.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Dizziness: transient light‑headedness.
  • Skin rash: erythematous or maculopapular eruptions.
  • Elevated liver enzymes: transient hepatic enzyme rise.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in white blood cells, requiring immediate medical attention.
  • Anaphylactic reaction: rapid onset of airway swelling, hypotension, and urticaria.

Precautions & Warnings

Metagelan should be used with caution in specific patient populations and clinical situations.

  • Renal impairment: assess kidney function before initiating therapy.
  • Hepatic disease: monitor liver enzymes during treatment.
  • Hematologic disorders: avoid in patients with a history of agranulocytosis.
  • Concomitant NSAIDs: increase risk of gastrointestinal bleeding.
  • Pregnancy and breastfeeding: use only if the potential benefit justifies the potential risk.
  • Store at ambient temperature: keep below 25°C, in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Metagelan can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): heightened bleeding risk.
  • Immunosuppressants (e.g., azathioprine): may exacerbate bone‑marrow suppression.

Moderate Interactions (Monitor Closely)

  • Other NSAIDs or COX inhibitors: additive gastrointestinal toxicity.
  • Diuretics: possible reduction in renal clearance.
  • Lithium: increased lithium levels may occur.
  • Methotrexate: enhanced toxicity risk.

Frequently Asked Questions

Metagelan contains Metamizole Sodium Monohydrate and is indicated for the relief of moderate to severe pain, reduction of fever, postoperative discomfort, and visceral pain such as colic. It is prescribed when other analgesics are insufficient or not tolerated.

The active ingredient inhibits cyclo‑oxygenase enzymes throughout the body, lowering prostaglandin synthesis. This reduces inflammation, pain signaling, and fever generation. Additionally, it influences central nervous system pathways that modulate pain perception, providing both peripheral and central analgesic effects.

The dosage of Metagelan is determined by the prescribing clinician based on the severity of pain or fever, patient age, weight, renal and hepatic function, and other individual factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Metagelan in pregnancy and lactation are limited. It should only be used if the potential therapeutic benefit outweighs any possible risk to the fetus or infant, and only under direct medical supervision.

To place an order, submit an enquiry on the Metagelan 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.

Metagelan belongs to the pyrazolone class, offering both analgesic and antipyretic effects similar to NSAIDs but with a distinct mechanism of non‑selective COX inhibition. Compared with opioids, it provides pain relief without the risk of dependence, though it carries a rare risk of agranulocytosis not seen with many NSAIDs.

Metagelan should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original container, protect it from moisture, direct sunlight, and extreme temperatures to maintain stability.

Metagelan is taken orally as directed by a healthcare professional. It may be administered with or without food, but patients should follow the prescriber’s guidance regarding timing and any accompanying fluids.

The most serious adverse reactions include agranulocytosis, a severe drop in white blood cells that can lead to infection, and anaphylactic shock. Immediate medical attention is required if symptoms such as fever, sore throat, or signs of allergic reaction appear.

Metagelan is contraindicated in individuals with a known hypersensitivity to Metamizole or other pyrazolones, patients with a history of agranulocytosis, and those with severe hepatic or renal impairment unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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