Product image of Narcaricin Mite (Benzbromarone) supplied by GNH India

Narcaricin Mite

Active Ingredient:
Benzbromarone
Origin:
EU

Narcaricin Mite (Benzbromarone)

Benzbromarone, the active ingredient in Narcaricin Mite, is a uricosuric agent presented as an oral tablet for oral use. It treats gout, hyperuricemia and related conditions in adult patients.
GNH India supplies Narcaricin Mite as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sano Arzneimittel Gmbh

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Indications & Clinical Uses

Narcaricin Mite, a uricosuric agent, is employed in the management of disorders associated with elevated uric acid levels.

  • Gout: reduces the frequency of acute attacks by lowering serum uric acid.
  • Hyperuricemia: maintains uric acid concentrations within target range to prevent disease progression.
  • Uric acid nephrolithiasis: facilitates dissolution and prevents formation of uric acid kidney stones.

How It Works

  • Benzbromarone inhibits the renal tubular reabsorption of uric acid by blocking the URAT1 transporter located in the proximal tubule. This blockade increases urinary excretion of uric acid, thereby lowering serum urate concentrations and helping to prevent crystal deposition in joints and kidneys.

Side Effects

Adverse reactions may occur with benzbromarone therapy.

Common Side Effects

  • Gastrointestinal upset: nausea, dyspepsia, or abdominal discomfort.
  • Skin reactions: mild rash or pruritus.
  • Headache: transient episodes of mild to moderate intensity.
  • Dizziness: occasional light‑headedness.
  • Elevated liver enzymes: mild, transient increases in hepatic transaminases.

Serious or Rare Side Effects

  • Severe hepatic injury: hepatitis or liver failure requiring monitoring.
  • Blood dyscrasias: agranulocytosis, leukopenia, or thrombocytopenia.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Acute renal failure: especially in patients with pre‑existing renal impairment.
  • Severe hypersensitivity reactions: anaphylaxis or serum sickness‑like syndrome.

Precautions & Warnings

Before initiating therapy, consider the following precautions.

  • Renal impairment: adjust use and monitor renal function regularly.
  • Hepatic dysfunction: avoid in patients with active liver disease and monitor liver enzymes.
  • Gout flare risk: prophylactic anti‑inflammatory therapy may be needed during initiation.
  • Drug interactions: review concomitant medications for potential interactions.
  • Pregnancy and lactation: safety not established; use only if benefits outweigh risks.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture.

Avoid Interactions

Benzbromarone may interact with several medicines; categorize as follows.

Major Interactions (Avoid)

  • Azathioprine: increased risk of bone‑marrow suppression.
  • Other uricosurics (e.g., probenecid): additive effect on uric acid excretion, raising toxicity risk.
  • Strong CYP2C9 inhibitors (e.g., fluconazole): elevate benzbromarone plasma levels.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may affect renal clearance of uric acid.
  • Diuretics (thiazides): can reduce uricosuric efficacy.
  • ACE inhibitors or ARBs: monitor blood pressure and renal function.
  • Anticoagulants: potential alteration of INR, require periodic testing.
  • Allopurinol: combined urate‑lowering effect may necessitate dose adjustment.

Frequently Asked Questions

Narcaricin Mite contains benzbromarone, a uricosuric medication prescribed to lower serum uric acid. It is used in the management of gout, chronic hyperuricemia, and uric acid kidney stones, helping to reduce flare frequency and prevent crystal deposition.

Benzbromarone blocks the URAT1 transporter in the renal proximal tubule, which normally reabsorbs uric acid. By inhibiting this transporter, the drug increases urinary excretion of uric acid, thereby lowering blood urate levels and reducing the risk of gout attacks and stone formation.

The dosage of Narcaricin Mite is individualized by the prescribing clinician based on the patient’s uric acid levels, renal function, and overall health status. The prescriber determines the appropriate strength and frequency, and patients should follow the written prescription exactly.

Safety data for benzbromarone in pregnancy and lactation are limited, and the product is generally not recommended for use in these populations. It should only be considered if the potential benefit justifies the possible risk to the fetus or infant, and under close medical supervision.

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.

Allopurinol reduces uric acid production, whereas benzbromarone (Narcaricin Mite) enhances uric acid excretion. Benzbromarone may be preferred in patients who do not achieve target urate levels with xanthine oxidase inhibitors or who have contraindications to allopurinol, but it requires careful monitoring of liver and kidney function.

Narcaricin Mite tablets should be stored at ambient temperature, below 25 °C. Keep them in the original container, protect from moisture and direct sunlight, and ensure they are out of reach of children.

The medication is taken orally as a tablet, usually with a full glass of water. It can be taken with or without food, but patients should follow the specific timing instructions provided by their healthcare professional.

Serious adverse events include severe liver injury, blood dyscrasias such as agranulocytosis, and rare hypersensitivity reactions like Stevens‑Johnson syndrome. Patients should be monitored regularly for hepatic and hematologic abnormalities, and any signs of severe reaction require immediate medical attention.

Narcaricin Mite is contraindicated in individuals with known hypersensitivity to benzbromarone, severe hepatic impairment, or active kidney disease that limits uric acid excretion. Caution is also advised for patients with a history of gallstones or those taking interacting medications listed under major interactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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