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 injectable solution for intramuscular and intravenous use. It provides analgesic, antipyretic, and antispasmodic effects for the treatment of moderate to severe pain, high fever, and smooth‑muscle spasm in adult patients. The product conforms to EU pharmacopeial standards and is manufactured under GMP conditions.

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

Manufacturer / TM Owner

Sun-Farm Sp. Z.O.O.

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Indications & Clinical Uses

Metamizole sodium is indicated for conditions where rapid analgesic, antipyretic, or antispasmodic control is required.

  • Pain: provides rapid relief of moderate to severe acute pain, including postoperative and trauma‑related pain.
  • Fever: reduces high fever when other antipyretics are insufficient or contraindicated.
  • Spasm: alleviates smooth‑muscle spasm associated with gastrointestinal or biliary colic.

How It Works

  • Metamizole sodium acts by non‑selectively inhibiting cyclooxygenase enzymes, which decreases the synthesis of prostaglandins involved in pain, fever, and inflammation. The reduction of prostaglandin E2 and other mediators leads to diminished peripheral nociceptor sensitisation and central fever regulation, while additional effects on calcium channels contribute to its antispasmodic activity.

Side Effects

Metamizole sodium may be associated with a range of adverse reactions, varying from mild to potentially life‑threatening.

Common Side Effects

  • Nausea: mild to moderate nausea reported after injection.
  • Vomiting: occasional episodes of vomiting.
  • Dizziness: transient light‑headedness or vertigo.
  • Hypotension: transient drop in blood pressure, especially with rapid IV administration.
  • Rash: mild skin erythema or urticaria.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in neutrophil count, potentially fatal if not detected.
  • Anaphylaxis: rare severe allergic reaction with respiratory compromise.
  • Severe hypotension: profound blood pressure fall requiring intervention.
  • Hepatotoxicity: rare liver enzyme elevations.
  • Stevens‑Johnson syndrome: extremely rare severe skin reaction.

Precautions & Warnings

When prescribing Metamizole sodium, clinicians should consider several safety measures to minimise risk.

  • Monitor blood counts: regular complete blood count monitoring is advised to detect agranulocytosis early.
  • Use caution in renal impairment: adjust dosing or monitor renal function in patients with reduced kidney function.
  • Avoid rapid IV bolus: administer intravenously over several minutes to reduce hypotension risk.
  • Contraindicated in known hypersensitivity: do not use in patients with previous allergic reactions to pyrazolones.
  • Caution in patients with cardiovascular disease: monitor blood pressure due to possible hypotensive effects.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Metamizole sodium can interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Myelosuppressive agents: concurrent use may increase risk of severe neutropenia or agranulocytosis.
  • Other pyrazolones or NSAIDs: additive risk of blood dyscrasias and gastrointestinal irritation.
  • ACE inhibitors: may potentiate hypotensive effects when combined with rapid IV administration.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): may enhance anticoagulant effect, requiring INR monitoring.
  • Diuretics: potential for enhanced hypotension, monitor blood pressure.
  • Antihypertensives: may require dose adjustment due to additive blood pressure lowering.
  • Lithium: possible increase in lithium levels, monitor serum concentrations.

Frequently Asked Questions

Metamizol Sf contains metamizole sodium, which is prescribed to manage moderate to severe acute pain, high fever that does not respond to other antipyretics, and smooth‑muscle spasm such as biliary or gastrointestinal colic. It is used in hospital settings where rapid intravenous or intramuscular relief is required.

Metamizole sodium works by non‑selectively inhibiting cyclooxygenase enzymes, leading to reduced prostaglandin synthesis. Lower prostaglandin levels decrease peripheral nociceptor sensitisation, suppress central fever mechanisms, and contribute to antispasmodic activity through calcium‑channel modulation.

The dose of Metamizol Sf is determined by the prescribing clinician based on the patient’s condition, severity of symptoms, and route of administration. Healthcare professionals adjust the amount and frequency according to clinical guidelines and individual response.

Safety data for metamizole sodium during pregnancy and lactation are limited, and the pregnancy category is listed as unknown. Caution is advised, and the drug should only be used if the potential benefit justifies any possible risk to the fetus or infant.

To order Metamizol Sf, submit an enquiry on the product page at gnhindia.com with 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.

Metamizole offers rapid analgesic and antipyretic effects similar to NSAIDs but with a different safety profile. Unlike opioids, it does not cause respiratory depression, but it carries a risk of agranulocytosis, which is rare with most NSAIDs. Choice of therapy depends on efficacy needs, patient comorbidities, and risk assessment.

Metamizol Sf should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. The product should be used within the expiry date indicated on the label and handled in accordance with aseptic techniques for injectable medicines.

Metamizol Sf is supplied as a sterile injectable solution for intramuscular or intravenous administration. The route and rate of injection are determined by the prescriber; intravenous doses are typically given slowly over several minutes to minimise the risk of hypotension.

The most serious adverse reactions include agranulocytosis, which can be life‑threatening if not detected early, severe hypotension especially after rapid IV injection, and rare anaphylactic reactions. Patients should be monitored for signs of infection, sudden drop in blood pressure, or allergic symptoms.

Metamizol Sf is contraindicated in individuals with known hypersensitivity to metamizole or other pyrazolones, in patients with a history of agranulocytosis, and in those with severe cardiovascular instability where hypotension could be dangerous. Caution is also advised for patients with renal impairment or active infections.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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