Product image of Novalgine I.M./I.V. (Metamizole Sodium Monohydrate) supplied by GNH India

Novalgine I.M./I.V.

Active Ingredient:
Metamizole Sodium Monohydrate
Origin:
EU

Novalgine I.M./I.V. (Metamizole Sodium Monohydrate)

Metamizole, the active ingredient in Novalgine I.M./I.V., is a pyrazolone derivative presented as an injectable solution for intramuscular and intravenous use. It treats pain and fever in adult patients, providing rapid relief in acute settings.

GNH India supplies Novalgine I.M./I.V. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Opella Healthcare Belgium (Handelsnaam Sanofi Belgium)

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Indications & Clinical Uses

Metamizole is employed for analgesic and antipyretic management in conditions where inflammation‑mediated pain or fever is present.

  • Pain: provides rapid relief of moderate to severe acute pain.
  • Fever: reduces elevated body temperature in febrile states.
  • Post‑operative analgesia: supports pain control after surgical procedures.
  • Acute musculoskeletal pain: offers effective analgesia for injuries and strain.

How It Works

  • Metamizole inhibits cyclooxygenase activity, leading to reduced synthesis of prostaglandins that mediate pain and fever. It may also interact with endogenous opioid pathways, enhancing analgesic effects without engaging opioid receptors. The combined actions result in lowered inflammatory signaling and temperature regulation.

Side Effects

Adverse reactions may occur with Metamizole use.

Common Side Effects

  • Injection site pain: mild discomfort at the site of administration.
  • Nausea: transient upset stomach.
  • Dizziness: occasional light‑headedness.
  • Flushing: brief skin reddening.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction of white blood cells.
  • Anaphylaxis: life‑threatening allergic reaction.
  • Stevens‑Johnson syndrome: severe skin and mucous membrane disorder.
  • Hepatic failure: marked liver dysfunction.

Precautions & Warnings

Careful assessment and monitoring are required when using Metamizole.

  • Assess renal function: adjust use in severe renal impairment.
  • Monitor blood counts: risk of agranulocytosis warrants periodic CBC.
  • Avoid in known hypersensitivity to pyrazolones.
  • Use cautiously in patients with cardiovascular disease due to hypotension risk.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Metamizole can interact with several drug classes; awareness of interaction severity helps guide safe use.

Major Interactions (Avoid)

  • Concurrent myelosuppressive agents: increased risk of agranulocytosis.
  • Other NSAIDs: additive gastrointestinal and renal toxicity.
  • ACE inhibitors: may enhance hypotensive effect.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): may increase bleeding tendency.
  • Diuretics: potential for reduced renal perfusion.
  • Lithium: may raise lithium serum concentrations.

Frequently Asked Questions

Novalgine I.M./I.V. contains metamizole sodium monohydrate and is indicated for the treatment of moderate to severe acute pain, reduction of fever, and as part of post‑operative analgesic regimens in adult patients. It is administered by intramuscular or intravenous injection under medical supervision.

Metamizole works by inhibiting cyclooxygenase enzymes, which decreases the production of prostaglandins that sensitize nerve endings and raise body temperature. It may also modulate endogenous opioid pathways, enhancing analgesic effects without directly activating opioid receptors.

The specific dose of Novalgine I.M./I.V. is determined by the prescribing clinician based on the patient’s condition, weight, renal function, and response to therapy. Healthcare professionals follow local guidelines and adjust the regimen as needed.

Safety data for metamizole in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Clinicians should weigh potential benefits against risks and consider alternative therapies when treating pregnant or nursing patients.

To place an order, 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 (including cold‑chain if needed) and import documentation.

Compared with traditional NSAIDs, metamizole offers potent analgesic and antipyretic effects with a lower incidence of gastrointestinal irritation but carries a unique risk of agranulocytosis. Selection depends on the clinical scenario, patient risk factors, and the therapeutic profile required by the prescriber.

Novalgine I.M./I.V. should be stored at ambient temperature, preferably below 25 °C, in its original packaging to protect from moisture and light. The solution must be inspected for particulate matter before administration and used within the expiry date.

The product is supplied as a sterile injectable solution for intramuscular or intravenous injection. Administration is performed by qualified healthcare personnel using aseptic technique, with dosage and rate of infusion determined by the treating physician.

The most serious risks include agranulocytosis, which can lead to severe infections, and rare hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome. Prompt monitoring of blood counts and immediate medical attention for any signs of severe allergic reaction are essential.

Novalgine I.M./I.V. is contraindicated in patients with known hypersensitivity to metamizole or other pyrazolones, in individuals with a history of agranulocytosis, and in those with severe hepatic or renal impairment where the risk outweighs benefit. Clinical judgment is required for all other cases.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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