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

Metamizol Medreg

Active Ingredient:
Metamizole Sodium Monohydrate
Origin:
EU

Metamizol Medreg (Metamizole Sodium Monohydrate)

Metamizole, the active ingredient in Metamizol Medreg, is a pyrazolone presented as an oral formulation for oral use. It provides analgesic and antipyretic effects for the treatment of pain and fever in adult patients, commonly prescribed after surgery or for acute febrile episodes.

GNH India supplies Metamizol Medreg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product meets European Union quality standards and is distributed under strict regulatory compliance.

Manufacturer / TM Owner

Medreg S.R.O.

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Indications & Clinical Uses

Metamizole is used to manage pain and fever through its action on prostaglandin synthesis and opioid pathways.

  • Pain: Reduces moderate to severe acute pain, including postoperative discomfort.
  • Fever: Lowers elevated body temperature in febrile conditions.
  • Postoperative pain: Provides analgesia after surgical procedures.

How It Works

  • Metamizole inhibits cyclooxygenase enzymes, reducing prostaglandin synthesis, and simultaneously modulates endogenous opioid pathways. This dual action diminishes nociceptive signaling and lowers the hypothalamic set‑point for temperature regulation, resulting in analgesic and antipyretic effects without significant anti‑inflammatory activity.

Side Effects

Metamizole may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Vomiting: occasional episodes after dosing.
  • Dizziness: transient light‑headedness.
  • Rash: mild skin erythema or pruritus.
  • Elevated liver enzymes: mild, reversible changes.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in white blood cells, potentially life‑threatening.
  • Anaphylactic reaction: rapid onset of airway swelling and hypotension.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Before prescribing Metamizole, clinicians should consider patient‑specific factors and monitor for adverse events.

  • Renal function: assess and monitor in patients with kidney impairment.
  • Hepatic function: evaluate liver enzymes prior to initiation.
  • Hematologic status: perform baseline complete blood count and monitor for neutropenia.
  • Concomitant medications: review for drugs that may increase bleeding risk.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit assessment.
  • Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Metamizole can interact with several drug classes; interactions vary in clinical significance.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Methotrexate: enhanced toxicity due to reduced renal clearance.
  • Cyclosporine: potential for nephrotoxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs: additive gastrointestinal irritation.
  • Lithium: possible increase in lithium serum levels.
  • ACE inhibitors or ARBs: monitor renal function and potassium levels.

Frequently Asked Questions

Metamizol Medreg contains metamizole sodium, an analgesic and antipyretic indicated for the relief of moderate to severe pain, reduction of fever, and management of postoperative discomfort in adult patients.

Metamizole exerts its effect by inhibiting cyclooxygenase enzymes, which reduces prostaglandin production, and by modulating endogenous opioid pathways, leading to decreased pain perception and lowered body temperature.

The specific dose and dosing schedule of Metamizol Medreg are determined by the prescribing clinician based on the patient’s condition, severity of symptoms, and individual response.

Safety in pregnancy and lactation has not been definitively established. It should only be used when the potential benefit justifies any possible risk to the fetus or infant, after careful medical evaluation.

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 and any necessary import documentation.

Compared with traditional NSAIDs, metamizole offers potent analgesia and antipyresis with a lower risk of gastrointestinal ulceration, but it carries a rare risk of agranulocytosis. Choice of therapy should consider efficacy, safety profile, and patient‑specific factors.

Metamizol Medreg should be stored at ambient temperature, below 25 °C, in its original packaging, protected from moisture and direct sunlight. Keep out of reach of children.

Metamizol Medreg is administered orally. The tablet should be swallowed whole with water and taken exactly as prescribed by the healthcare professional.

The most serious adverse reactions include agranulocytosis, which can lead to severe infection, and anaphylactic shock. Immediate medical attention is required if signs of severe allergic reaction or unexplained fever occur.

Metamizol Medreg is contraindicated in patients with known hypersensitivity to metamizole or other pyrazolones, in individuals with a history of agranulocytosis, and in patients with severe liver or kidney impairment unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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