Product image of Metamizol Stada (Metamizole) supplied by GNH India

Metamizol Stada

Active Ingredient:
Metamizole
Origin:
EU

Metamizol Stada (Metamizole)

Metamizole, the active ingredient in Metamizol Stada, is a pyrazolone presented as an oral formulation for oral use. It is employed to relieve pain, reduce fever, and provide post‑operative analgesia in adult patients and is approved for use in the European Union market.

GNH India supplies Metamizol Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and procurement teams worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support import and distribution across multiple regions.

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

Metamizole acts on the cyclooxygenase pathway and is indicated for several acute pain and fever conditions.

  • Pain relief: Provides analgesic effect for moderate to severe acute pain, such as musculoskeletal injuries or dental pain.
  • Fever reduction: Lowers elevated body temperature in febrile states, including infection‑related fever.
  • Post‑operative analgesia: Controls pain following surgical procedures, facilitating recovery and patient comfort.
  • Severe cancer‑related pain: Offers additional analgesia when other agents are insufficient.

How It Works

  • Metamizole inhibits cyclooxygenase (COX) enzymes, reducing prostaglandin synthesis, and simultaneously modulates endogenous opioid pathways. The combined effect decreases peripheral and central sensitization to pain stimuli and lowers the hypothalamic set‑point for temperature regulation, resulting in analgesic and antipyretic actions. Additionally, Metamizole may influence calcium channels and nitric oxide production, contributing further to its analgesic profile. These mechanisms together provide rapid onset of pain relief and fever control in acute settings.

Side Effects

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

Common Side Effects

  • Nausea: mild gastrointestinal upset that may resolve without intervention.
  • Vomiting: occasional emesis that can be managed with anti‑emetics.
  • Dizziness: transient light‑headedness, often occurring shortly after dosing.
  • Skin rash: mild erythematous reactions, usually limited to localized areas.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction of neutrophils leading to increased infection risk; requires immediate medical attention.
  • Anaphylaxis: acute allergic reaction with respiratory distress, hypotension, and possible shock; emergency treatment is essential.
  • Stevens‑Johnson syndrome: rare severe skin eruption with blistering and mucosal involvement, necessitating prompt discontinuation of the drug.

Precautions & Warnings

When prescribing Metamizole, several precautions should be observed to minimize risk.

  • Blood monitoring: regular complete blood counts are recommended to detect agranulocytosis early.
  • Renal function: assess kidney function, especially in patients with pre‑existing impairment.
  • Hepatic function: evaluate liver enzymes as Metamizole is metabolized hepatically.
  • Concomitant drugs: avoid use with other myelosuppressive agents without supervision.
  • Pregnancy and lactation: use only if benefits outweigh potential risks, as safety data are limited.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Metamizole can interact with other medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Anticoagulants: may enhance bleeding risk; concurrent use requires close monitoring.
  • Immunosuppressants: combined myelosuppression can increase risk of severe neutropenia.

Moderate Interactions (Monitor Closely)

  • NSAIDs: additive gastrointestinal irritation and potential renal effects.
  • Antihypertensives: may reduce antihypertensive efficacy due to fluid shifts.
  • Diuretics: increased risk of electrolyte imbalance when combined.

Frequently Asked Questions

Metamizol Stada contains the active ingredient Metamizole, which is used to relieve moderate to severe acute pain, reduce fever, and provide postoperative analgesia. It is commonly prescribed in hospital and clinic settings for conditions such as musculoskeletal pain, dental pain, febrile illnesses, and after surgical procedures.

Metamizole works by inhibiting cyclooxygenase enzymes, which reduces the production of prostaglandins that mediate pain and fever. It also modulates endogenous opioid pathways and may affect calcium channels and nitric‑oxide production, together decreasing peripheral and central pain sensitisation and lowering the hypothalamic set‑point for body temperature.

The appropriate dose of Metamizol Stada is determined by the prescribing healthcare professional based on the patient’s age, weight, severity of pain or fever, and overall clinical condition. Dosage regimens are individualized and should follow the prescriber’s instructions and local regulatory guidelines.

Safety data for Metamizole during pregnancy and lactation are limited. It should only be used when the potential therapeutic benefit justifies the possible risk to the fetus or infant. Healthcare providers should evaluate the risk‑benefit profile carefully before prescribing to pregnant or nursing women.

To order Metamizol Stada, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials. After confirmation, the team provides pricing, availability, shipping details (including any cold‑chain requirements) and assists with import documentation.

Metamizole belongs to the pyrazolone class, offering both analgesic and antipyretic effects. Compared with non‑steroidal anti‑inflammatory drugs (NSAIDs), it has a lower risk of gastrointestinal ulceration but carries a rare risk of agranulocytosis. Unlike opioids, it does not produce significant respiratory depression, making it a useful alternative for certain acute pain scenarios.

Metamizol Stada should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, direct sunlight, and extreme temperatures. Ensure the container is tightly closed to maintain stability and prevent contamination.

Metamizol Stada is administered orally. The tablet or oral formulation is taken with water, usually after a meal to minimise gastrointestinal discomfort. The exact timing and frequency are determined by the prescribing clinician based on the individual’s therapeutic needs.

The most serious adverse reactions associated with Metamizole are agranulocytosis, a potentially life‑threatening drop in white‑blood‑cell count, and severe allergic responses such as anaphylaxis or Stevens‑Johnson syndrome. Patients should be instructed to seek immediate medical attention if they develop signs of infection, unexplained fever, rash, or breathing difficulties.

Metamizole is contraindicated in individuals with known hypersensitivity to the drug or other pyrazolones, patients with a history of agranulocytosis, and those receiving concurrent myelosuppressive therapy without close monitoring. Caution is also advised for patients with severe liver or kidney impairment, and it should be avoided in pregnancy unless clearly justified.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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