Product image of Metamizol-Sf (Metamizole Sodium Monohydrate) supplied by GNH India

Metamizol-Sf

Active Ingredient:
Metamizole Sodium Monohydrate
Origin:
EU

Metamizol-Sf (Metamizole Sodium Monohydrate)

Metamizole sodium, the active ingredient in Metamizol‑Sf, is a pyrazolone presented as a sterile solution for intramuscular and intravenous use. It provides analgesic and antipyretic effects, indicated for the management of moderate to severe pain and for fever reduction in adult patients.

GNH India supplies Metamizol‑Sf as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent product quality, regulatory compliance, and reliable logistics for global healthcare providers.

Manufacturer / TM Owner

Sun-Farm Sp. Z.O.O.

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Indications & Clinical Uses

Metamizole sodium acts as an analgesic and antipyretic within the pyrazolone class, addressing pain and fever pathways.

  • Acute pain: delivers rapid analgesia for postoperative or trauma‑related pain.
  • High fever: lowers elevated body temperature when other antipyretics are insufficient.
  • Colicky abdominal pain: eases spasm‑related discomfort in gastrointestinal conditions.

How It Works

  • Metamizole sodium exerts its effect by non‑selectively inhibiting cyclooxygenase enzymes, which reduces prostaglandin synthesis. The decrease in prostaglandins diminishes peripheral sensitization to pain and lowers the hypothalamic set‑point for temperature regulation, while central actions contribute to analgesia and spasmolysis.

Side Effects

Metamizole sodium may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Dizziness: transient light‑headedness after injection.
  • Injection site pain: local discomfort at the administration site.
  • Rash: mild skin erythema or itching.
  • Hypotension: occasional drop in blood pressure.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in white blood cells, requiring immediate medical attention.
  • Aplastic anemia: bone‑marrow failure leading to pancytopenia.
  • Stevens‑Johnson syndrome: severe mucocutaneous reaction.
  • Anaphylaxis: acute, potentially life‑threatening allergic response.
  • Hepatic dysfunction: abnormal liver enzyme elevations.

Precautions & Warnings

When using Metamizole‑Sf, consider the following safety measures.

  • Renal impairment: use with caution and monitor renal function.
  • Hepatic disease: assess liver status before initiation.
  • History of blood disorders: avoid in patients with prior agranulocytosis or aplastic anemia.
  • Concomitant myelosuppressive therapy: increase monitoring for bone‑marrow toxicity.
  • Pregnancy and lactation: prescribe only if potential benefit justifies the risk.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Metamizole‑Sf can interact with several drug classes; awareness helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Cytotoxic chemotherapy: additive risk of bone‑marrow suppression.
  • Anticoagulants (e.g., warfarin): potential enhancement of bleeding.
  • Sulfonamides: increased likelihood of blood dyscrasias.

Moderate Interactions (Monitor Closely)

  • NSAIDs: possible additive renal toxicity.
  • ACE inhibitors: may potentiate hypotensive effects.
  • Diuretics: monitor electrolytes for disturbances.

Frequently Asked Questions

Metamizol‑Sf contains metamizole sodium, a pyrazolone that provides analgesic and antipyretic effects. It is used to treat moderate to severe pain, such as postoperative or trauma‑related pain, and to reduce high fever when other antipyretics are inadequate.

Metamizole sodium works by non‑selectively inhibiting cyclooxygenase enzymes, which lowers prostaglandin production. This reduction diminishes peripheral pain signaling and resets the hypothalamic temperature set‑point, while central mechanisms add to its analgesic and spasmolytic actions.

The appropriate dose of Metamizol‑Sf is determined by the prescribing clinician based on the patient’s condition, age, weight, and renal or hepatic function. Dosage regimens are individualized and should follow local prescribing guidelines.

Safety data for metamizole sodium in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used when the potential benefit outweighs any possible risk to the mother or infant, and under medical supervision.

To order Metamizol‑Sf, 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‑Sf belongs to the pyrazolone class, offering both analgesic and antipyretic activity. Compared with NSAIDs, it has a lower risk of gastrointestinal irritation but carries a rare risk of severe blood dyscrasias. Unlike opioids, it does not cause respiratory depression, making it a useful alternative for certain pain scenarios.

Metamizol‑Sf should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and extreme temperature fluctuations to maintain stability and potency.

Metamizol‑Sf is supplied as a sterile injectable solution and can be given either intramuscularly or intravenously by a qualified healthcare professional. The route and rate of administration are determined by the prescriber according to the clinical situation.

The most serious risks include agranulocytosis and aplastic anemia, both of which are rare but potentially life‑threatening blood disorders. Early signs such as unexplained fever, sore throat, or infections should prompt immediate medical evaluation.

Metamizol‑Sf is contraindicated in patients with a known hypersensitivity to metamizole or other pyrazolones, those with a history of agranulocytosis or severe bone‑marrow suppression, and individuals with severe hepatic or renal impairment unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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