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

Metamizol Stada

Active Ingredient:
Metamizole Sodium Monohydrate
Origin:
EU

Metamizol Stada (Metamizole Sodium Monohydrate)

Metamizole, the active ingredient in Metamizol Stada, is a pyrazolone derivative presented as an oral formulation for systemic use. It is employed to relieve mild to moderate pain, reduce fever, and manage postoperative discomfort and colic in adult patients.
GNH India supplies Metamizol Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Metamizole acts as a non‑opioid analgesic and antipyretic, targeting pain and fever pathways.

  • Mild to moderate pain: provides effective relief when other analgesics are insufficient.
  • Fever: reduces elevated body temperature in acute febrile states.
  • Post‑operative pain: helps control discomfort after surgical procedures.
  • Colic: alleviates visceral pain associated with intestinal or biliary colic.

How It Works

  • Metamizole sodium monohydrate inhibits cyclooxygenase‑mediated prostaglandin synthesis, decreasing peripheral sensitisation of nociceptors. It also modulates central pain pathways, likely through interaction with spinal and supraspinal receptors, resulting in analgesic and antipyretic effects without opioid receptor involvement.

Side Effects

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

Common Side Effects

  • Nausea: transient gastrointestinal upset.
  • Vomiting: occasional emesis following dose.
  • Dizziness: mild vertiginous sensation.
  • Hypotension: transient drop in blood pressure, especially with rapid administration.
  • Skin rash: mild erythematous eruption.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in neutrophils, potentially life‑threatening.
  • Anaphylactic reaction: rapid onset of airway swelling and hypotension.
  • Stevens‑Johnson syndrome: severe mucocutaneous blistering.
  • Hemolytic anemia: destruction of red blood cells.
  • Hepatic dysfunction: elevated liver enzymes indicating liver injury.

Precautions & Warnings

Metamizole should be used with caution and under medical supervision.

  • Blood count monitoring: perform baseline and periodic leukocyte counts to detect agranulocytosis early.
  • Hypersensitivity avoidance: do not use in patients with known allergy to pyrazolones.
  • Renal/hepatic impairment: adjust use and monitor organ function.
  • Pregnancy and lactation: avoid unless benefits outweigh potential risks.
  • Concomitant myelosuppressants: increase risk of bone‑marrow suppression.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Metamizole can interact with several drug classes, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Other myelosuppressive agents: heightened risk of agranulocytosis.
  • Known hypersensitivity to other pyrazolone derivatives: may trigger severe allergic response.

Moderate Interactions (Monitor Closely)

  • NSAIDs (e.g., ibuprofen, diclofenac): may diminish analgesic efficacy.
  • ACE inhibitors or diuretics: potential additive hypotensive effect.
  • Alcohol: can exacerbate dizziness and hypotension.
  • Anticoagulants (e.g., warfarin): possible increase in bleeding tendency.

Frequently Asked Questions

Metamizol Stada is prescribed to manage mild to moderate pain, reduce fever, alleviate postoperative discomfort, and treat colic-related visceral pain. It is a non‑opioid option for patients who need effective analgesia and antipyretic action, particularly when other medications are insufficient or contraindicated.

Metamizole works by inhibiting cyclooxygenase enzymes, which reduces the synthesis of prostaglandins that mediate pain and fever. Additionally, it influences central nervous system pathways that modulate pain perception, providing analgesic and antipyretic effects without engaging opioid receptors.

The exact dose of Metamizol Stada is determined by the prescribing clinician based on the patient’s condition, age, weight, and overall health. Healthcare professionals tailor the regimen to achieve optimal pain relief or fever control while minimizing potential risks.

Safety data for Metamizol Stada in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the possible risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

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 necessary import documentation.

Metamizol offers non‑opioid analgesia with both pain‑relieving and antipyretic properties, distinguishing it from NSAIDs that primarily target inflammation. Compared with opioids, it has a lower risk of respiratory depression but carries a unique risk of agranulocytosis, requiring blood‑count monitoring.

Metamizol Stada should be stored at ambient temperature, below 25 °C. Keep the product in its original packaging, protect it from moisture, and store it away from direct sunlight to maintain stability and potency.

Metamizol Stada is administered orally. The tablet is swallowed whole with water, unless the prescribing physician provides alternative instructions such as crushing for patients with swallowing difficulties. It should be taken exactly as directed by the healthcare professional.

The most serious risks include agranulocytosis, a potentially fatal drop in white blood cells, and severe allergic reactions such as anaphylaxis or Stevens‑Johnson syndrome. Prompt medical attention is required if signs of infection, rash, or breathing difficulty develop.

Metamizol Stada is contraindicated in individuals with known hypersensitivity to metamizole or other pyrazolone derivatives, patients with existing severe bone‑marrow suppression, and those who have experienced agranulocytosis with prior use. It should also be avoided in patients for whom safer alternatives are available.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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