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, the active ingredient in Metagelan, is a pyrazolone non‑opioid analgesic presented as a sterile injectable solution for intramuscular or intravenous use. It provides analgesic and antipyretic effects for moderate to severe pain, postoperative pain, colic and fever in adult patients.

GNH India supplies Metagelan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

G.L. Pharma Gmbh

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Indications & Clinical Uses

Metagelan is a non‑opioid analgesic used in conditions that require strong pain relief or fever reduction.

  • Moderate to severe pain: reduces intensity of acute or chronic pain.
  • Post‑operative pain: helps control pain after surgical procedures.
  • Colic: alleviates visceral pain associated with gastrointestinal spasm.
  • Fever: lowers elevated body temperature in adults.

How It Works

  • Metamizole Sodium acts by non‑selectively inhibiting cyclooxygenase enzymes, which decreases prostaglandin synthesis in peripheral tissues and the central nervous system. This inhibition provides both analgesic and antipyretic effects, while its spasmolytic activity reduces smooth‑muscle contractions contributing to visceral pain.

Side Effects

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

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the site of administration.
  • Nausea: transient feeling of queasiness.
  • Dizziness: temporary light‑headedness.
  • Hypotension: mild drop in blood pressure.
  • Rash: mild skin erythema.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in white blood cells, requiring immediate medical attention.
  • Anaphylaxis: rapid onset of allergic reaction with airway compromise.
  • Hepatotoxicity: liver enzyme elevations indicating possible liver injury.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hemolysis: breakdown of red blood cells in susceptible individuals.

Precautions & Warnings

Before using Metagelan, consider the following safety measures.

  • Renal impairment: adjust use in patients with reduced kidney function.
  • Hepatic disease: monitor liver function during therapy.
  • Hematologic disorders: avoid in patients with existing blood dyscrasias.
  • Allergy history: do not administer if the patient has known hypersensitivity to pyrazolones.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Metagelan can interact with several medicines; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Other myelosuppressive agents: heightened risk of agranulocytosis.
  • ACE inhibitors: may potentiate hypotensive effects.

Moderate Interactions (Monitor Closely)

  • NSAIDs: additive gastrointestinal irritation.
  • Diuretics: may enhance hypotensive response.
  • Lithium: possible increase in lithium serum levels.

Frequently Asked Questions

Metagelan contains Metamizole Sodium, a non‑opioid analgesic used to treat moderate to severe pain, postoperative pain, colic and fever in adult patients. It is administered by intramuscular or intravenous injection under medical supervision.

Metamizole Sodium works by non‑selectively inhibiting cyclooxygenase enzymes, which reduces prostaglandin synthesis. This action provides analgesic, antipyretic and spasmolytic effects, helping to lower pain intensity and body temperature.

The dosage of Metagelan is determined by the prescribing clinician based on the patient’s condition, severity of pain or fever, and individual health factors. Only a qualified healthcare professional should set the dose.

Safety data for Metagelan in pregnancy and lactation are limited. It should only be used if the potential benefit outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

To order Metagelan, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details and import documentation.

Metagelan (Metamizole Sodium) is a non‑opioid pyrazolone, offering strong analgesic and antipyretic effects without the opioid‑related risks of dependence. Compared with NSAIDs, it has a lower incidence of gastrointestinal irritation but carries a rare risk of agranulocytosis, requiring blood monitoring in long‑term use.

Metagelan should be stored at 2‑8 °C, kept refrigerated, protected from light, and not frozen. Maintain the product in its original packaging to preserve stability.

Metagelan is administered by a healthcare professional via intramuscular or intravenous injection. The route, injection site and rate are selected according to the clinical situation and prescribing information.

The most serious risks include agranulocytosis, a potentially life‑threatening drop in white blood cells, and severe allergic reactions such as anaphylaxis. Prompt medical attention is required if signs of infection, rash, breathing difficulty, or sudden fever occur.

Metagelan should be avoided in patients with known hypersensitivity to Metamizole or other pyrazolones, those with existing severe blood dyscrasias, and individuals with uncontrolled renal or hepatic impairment unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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