Product image of Metamizol Sodic Sopharma (Metamizole Sodium) supplied by GNH India

Metamizol Sodic Sopharma

Active Ingredient:
Metamizole Sodium
Origin:
EU

Metamizol Sodic Sopharma (Metamizole Sodium)

Metamizole sodium, the active ingredient in Metamizol Sodic Sopharma, is a pyrazolone presented as an injectable solution for intramuscular and intravenous use. It is employed to relieve moderate to severe pain, reduce fever, and provide postoperative analgesia, including treatment of colic.

GNH India supplies Metamizol Sodic Sopharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product conforms to EU quality standards and is distributed under strict regulatory oversight.

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Indications & Clinical Uses

  • Metamizole sodium is used in clinical settings to manage pain and fever through its analgesic and antipyretic actions.
  • Pain: provides rapid relief of moderate to severe acute pain
  • Fever: reduces elevated body temperature in febrile states
  • Postoperative analgesia: controls pain after surgical procedures
  • Colic: alleviates visceral pain associated with intestinal colic

How It Works

  • Metamizole sodium exerts its effect by non‑selectively inhibiting cyclooxygenase enzymes, which decreases the synthesis of prostaglandins involved in pain signaling and thermoregulation. The reduced prostaglandin levels diminish peripheral sensitization and central fever pathways, resulting in analgesic and antipyretic outcomes. Its exact binding profile remains partially characterized, but the COX inhibition is central to its therapeutic action.

Side Effects

Metamizole sodium may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Injection site pain: mild discomfort at the site of administration.
  • Nausea: transient feeling of queasiness.
  • Vomiting: occasional episodes.
  • Dizziness: light‑headed sensation.
  • Hypotension: temporary drop in blood pressure.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in white blood cells, potentially life‑threatening.
  • Anaphylaxis: acute allergic reaction with respiratory compromise.
  • Stevens‑Johnson syndrome: severe skin and mucous membrane disorder.
  • Hemolytic anemia: destruction of red blood cells.
  • Severe liver dysfunction: marked elevation of hepatic enzymes.

Precautions & Warnings

  • When using Metamizole sodium, clinicians should observe specific safety measures.
  • Assess blood counts: perform baseline and periodic complete blood count to monitor for agranulocytosis.
  • Avoid in known hypersensitivity: discontinue if allergic reactions occur.
  • Use caution in renal impairment: adjust monitoring as drug is renally excreted.
  • Limit duration: avoid prolonged use without medical supervision.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Metamizole sodium can interact with several drug classes; awareness of interaction severity guides clinical decisions.

Major Interactions (Avoid)

  • Concurrent use with other myelosuppressive agents: increased risk of agranulocytosis.
  • Combination with sulfonamides: heightened potential for severe blood dyscrasias.
  • Co‑administration with anticoagulants: may potentiate bleeding risk.
  • Use with other NSAIDs: additive gastrointestinal toxicity.
  • Interaction with CYP450 inhibitors: possible altered metabolism.

Moderate Interactions (Monitor Closely)

  • Concomitant antihypertensives: may enhance hypotensive effect.
  • Use with diuretics: monitor electrolyte balance.
  • Combination with other antipyretics: assess cumulative fever reduction.
  • Co‑administration with drugs affecting platelet function: monitor bleeding.
  • Interaction with immunosuppressants: observe for infection risk.

Frequently Asked Questions

Metamizol Sodic Sopharma, containing metamizole sodium, is indicated for the relief of moderate to severe pain, reduction of fever, postoperative analgesia, and management of visceral pain such as colic. It is administered by intramuscular or intravenous injection in hospital or clinical settings.

Metamizole sodium works by inhibiting cyclooxygenase enzymes, which leads to decreased production of prostaglandins. Lower prostaglandin levels reduce peripheral pain signaling and central thermoregulatory pathways, providing both analgesic and antipyretic effects.

The appropriate dose of Metamizol Sodic Sopharma is determined by the prescribing clinician based on the patient’s condition, age, weight, and clinical response. Healthcare professionals adjust the dosage to achieve effective pain or fever control while monitoring safety.

Safety data for metamizole sodium in pregnancy and lactation are limited, and the product is generally not recommended unless clearly needed. Clinicians should evaluate the risk‑benefit profile for each patient and consider alternative therapies when possible.

To request Metamizol Sodic Sopharma, 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 and any necessary import documentation.

Metamizole sodium belongs to the pyrazolone class and offers rapid analgesic and antipyretic effects, often with a lower incidence of gastrointestinal irritation compared with traditional NSAIDs. However, it carries a risk of severe blood disorders, which may be less common with some alternative agents.

Metamizole Sodic Sopharma should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Maintaining the cold chain preserves the stability and sterility of the injectable solution.

The product is supplied as a sterile injectable solution and is given either intramuscularly or intravenously by a qualified healthcare professional. Administration technique follows standard aseptic procedures and dosing recommendations provided by the prescriber.

The most serious adverse reactions include agranulocytosis, a potentially life‑threatening drop in white blood cells, and severe allergic responses such as anaphylaxis or Stevens‑Johnson syndrome. Prompt recognition and discontinuation are essential if these events occur.

Patients with known hypersensitivity to metamizole sodium or any pyrazolone, those with a history of severe blood dyscrasias, and individuals receiving concurrent myelosuppressive therapy should avoid this medication. Clinical judgment is required for patients with significant renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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