Product image of Nitroxolină Mip (Nitroxoline) supplied by GNH India

Nitroxolină Mip

Active Ingredient:
Nitroxoline
Origin:
EU

Nitroxolină Mip (Nitroxoline)

Nitroxoline, the active ingredient in Nitroxolină Mip, is a quinoline derivative antibacterial presented as an oral tablet for oral use. It treats uncomplicated urinary tract infections, including cystitis, in adult patients.
GNH India supplies Nitroxolină Mip as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Mip Pharma Gmbh

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Indications & Clinical Uses

Nitroxolină Mip is used to manage bacterial infections of the urinary tract.

  • Uncomplicated urinary tract infection: eliminates causative bacteria and relieves dysuria and frequency.
  • Cystitis: treats bladder infection, reducing inflammation and promoting symptom resolution.
  • Acute uncomplicated cystitis: provides rapid bacterial clearance and symptom improvement.

How It Works

  • Nitroxoline exerts its antibacterial effect by chelating divalent metal ions such as iron and magnesium, which are essential cofactors for bacterial enzymes. This chelation impairs bacterial adhesion, disrupts metabolic pathways, and inhibits key enzymes, leading to reduced bacterial growth and eventual eradication of susceptible urinary pathogens.

Side Effects

Nitroxolină Mip may cause adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Vomiting: occasional episodes after dosing.
  • Abdominal pain: cramp‑like discomfort in the gastrointestinal tract.
  • Headache: transient dull or throbbing pain.
  • Rash: mild skin erythema or pruritus.
  • Altered taste: metallic or bitter sensation.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction with airway compromise.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Neutropenia: marked reduction in white blood cells.
  • Thrombocytopenia: low platelet count leading to bleeding risk.
  • Stevens‑Johnson syndrome: severe skin blistering and mucosal involvement.
  • Interstitial nephritis: inflammation of kidney interstitium causing renal impairment.

Precautions & Warnings

Before prescribing Nitroxolină Mip, clinicians should consider several safety aspects.

  • Renal function: evaluate creatinine clearance in patients with kidney disease.
  • Hepatic function: monitor liver enzymes in individuals with liver impairment.
  • Pregnancy: use only if the potential benefit justifies the unknown risk to the fetus.
  • Elderly patients: start at the lowest effective dose and monitor for toxicity.
  • Concomitant medications: review all drugs for possible interactions.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Nitroxolină Mip can interact with other medicines, requiring careful assessment.

Major Interactions (Avoid)

  • Nephrotoxic agents (e.g., aminoglycosides): may increase risk of kidney injury.
  • Strong metal chelators (e.g., deferoxamine): can reduce nitroxoline absorption and efficacy.
  • Co‑administration with other quinolone antibiotics: risk of additive toxicity.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may heighten gastrointestinal irritation.
  • Warfarin: potential enhancement of anticoagulant effect, requiring INR monitoring.
  • Diuretics: possible electrolyte disturbances; monitor serum levels.

Frequently Asked Questions

Nitroxolină Mip contains nitroxoline, an oral antibacterial indicated for the treatment of uncomplicated urinary tract infections, including cystitis. It is prescribed to eradicate susceptible bacteria from the urinary system and relieve associated symptoms such as dysuria, frequency, and urgency.

Nitroxoline chelates essential metal ions like iron and magnesium, which are cofactors for bacterial enzymes. This chelation disrupts enzyme activity, impairs bacterial adhesion, and interferes with metabolic pathways, ultimately inhibiting bacterial growth and facilitating eradication of urinary pathogens.

The dosage of Nitroxolină Mip is determined by the prescribing healthcare professional based on the patient’s condition, age, renal function, and other clinical factors. Patients should follow the prescriber’s instructions and not alter the dose without medical advice.

The safety of nitroxoline in pregnancy and lactation has not been established. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

To request Nitroxolină Mip, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Nitroxoline belongs to the quinoline derivative class, offering a distinct mechanism of metal‑ion chelation compared with nitrofurantoin or fosfomycin, which act through bacterial DNA damage or cell‑wall synthesis inhibition. Clinical choice depends on local resistance patterns, patient tolerance, and specific infection characteristics.

Nitroxolină Mip tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture, heat and direct sunlight to maintain potency throughout the shelf life.

Nitroxolină Mip is taken orally with a full glass of water. The tablet should be swallowed whole and not crushed or chewed, unless otherwise directed by a healthcare professional. Administration is usually spaced evenly throughout the day as prescribed.

Serious adverse reactions, although rare, include severe allergic responses such as anaphylaxis, hepatic dysfunction, neutropenia, thrombocytopenia, Stevens‑Johnson syndrome and interstitial nephritis. Patients should seek immediate medical attention if they experience signs of these conditions.

Nitroxolină Mip is contraindicated in patients with known hypersensitivity to nitroxoline or any component of the formulation. Caution is also advised for individuals with severe renal or hepatic impairment, and it should be avoided in pregnant women unless clearly indicated by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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