Europe — EMA
Natrijev Metamizolat Krka (Metamizole Sodium Monohydrate)
GNH USA supplies Natrijev Metamizolat Krka (Metamizole Sodium), a pyrazolone analgesic for moderate to severe pain and high fever.
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What is Metamizole Sodium Monohydrate?
Metamizole sodium, the active ingredient in Natrijev Metamizolat Krka, is a pyrazolone derivative presented as a sterile injectable solution for intramuscular or intravenous use. It is employed to relieve moderate to severe pain and to reduce high fever in adult patients. GNH USA supplies Natrijev Metamizolat Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.
What is Metamizole Sodium Monohydrate used for?
Metamizole sodium is indicated for conditions where strong analgesia or antipyresis is required. - Moderate to severe pain: provides rapid pain relief when weaker analgesics are insufficient. - Post‑operative pain: helps control surgical pain during the immediate recovery period. - Colic: reduces visceral pain associated with gastrointestinal spasm. - High fever: lowers body temperature when antipyretic therapy is needed.
What are the side effects of Metamizole Sodium Monohydrate?
Metamizole sodium may cause a range of adverse reactions, from mild to severe.
Common Side Effects: - Injection site pain or erythema: local discomfort at the administration site. - Nausea or vomiting: gastrointestinal upset following dosing. - Dizziness or light‑headedness: transient vertigo or feeling faint. - Transient hypotension: temporary drop in blood pressure after rapid IV administration.
Serious or Rare Side Effects: - Agranulocytosis: severe reduction of neutrophils, increasing infection risk. - Severe skin reactions (e.g., Stevens‑Johnson syndrome): extensive rash or mucosal involvement. - Anaphylactic reaction: sudden, life‑threatening allergic response. - Hepatic enzyme elevation: abnormal liver function tests indicating possible liver injury.
What precautions apply to Metamizole Sodium Monohydrate?
Before initiating therapy, clinicians should assess patient suitability and monitor for adverse events. - Baseline blood count: obtain complete blood count to detect pre‑existing leukopenia. - Infection monitoring: watch for signs of infection, especially if agranulocytosis develops. - Hypersensitivity: avoid in patients with known allergy to pyrazolones or Metamizole. - Renal/hepatic impairment: use with caution and consider dose adjustment. - Pregnancy: limit use to situations where benefit outweighs potential risk. - Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.
What does Metamizole Sodium Monohydrate interact with?
Metamizole sodium can interact with several drug classes, requiring careful management.
Major Interactions (Avoid): - Other myelotoxic agents (e.g., chemotherapy): may compound risk of agranulocytosis. - Anticoagulants (e.g., warfarin): can enhance bleeding tendency. - Concurrent pyrazolone derivatives: increase risk of severe hematologic toxicity.
Moderate Interactions (Monitor Closely): - ACE inhibitors or diuretics: may potentiate hypotensive effects. - NSAIDs: additive renal stress and gastrointestinal irritation. - Alcohol: can exacerbate dizziness and hypotension.



