Product image of Nitrofurantoin Manx Healthcare (Nitrofurantoin, Macrocrystalline) supplied by GNH India

Nitrofurantoin Manx Healthcare

Active Ingredient:
Nitrofurantoin, Macrocrystalline
Origin:
EU

Nitrofurantoin Manx Healthcare (Nitrofurantoin, Macrocrystalline)

Nitrofurantoin, the active ingredient in Nitrofurantoin Manx Healthcare, is a nitrofuran antibiotic presented as a macrocrystalline oral tablet for oral use. The macrocrystalline formulation enhances stability and bioavailability, and the drug is employed to treat uncomplicated urinary tract infection (cystitis) in adult patients, providing bacterial eradication and symptom relief.

GNH India supplies Nitrofurantoin Manx Healthcare as a licensed, GDP‑compliant international pharmaceutical supplier, adhering to EU GMP standards and providing the product to hospitals, pharmacies and clinics worldwide through regulated distribution channels.

Manufacturer / TM Owner

Manx Healthcare Ltd

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Indications & Clinical Uses

  • Nitrofurantoin is a nitrofuran antibiotic used to manage infections of the urinary tract.
  • Uncomplicated urinary tract infection (cystitis): eliminates causative bacteria and alleviates urinary symptoms.
  • Prophylaxis of recurrent urinary tract infection: reduces the frequency of future infection episodes when taken long‑term.
  • Acute uncomplicated cystitis in women: provides rapid bacterial clearance and symptom improvement.

How It Works

  • Nitrofurantoin exerts its antibacterial effect by entering bacterial cells and inhibiting enzymes involved in carbohydrate metabolism, particularly the bacterial electron transport chain. This disruption impairs synthesis of nucleic acids and proteins, leading to bacterial cell death, especially in Gram‑negative uropathogens such as Escherichia coli. The drug is rapidly excreted unchanged in the urine, achieving high concentrations that exceed the minimum inhibitory concentrations for common uropathogens, thereby enhancing its therapeutic efficacy in the urinary tract.

Side Effects

Nitrofurantoin may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Nausea: mild stomach upset that may occur after dosing.
  • Diarrhea: loose stools, often transient.
  • Headache: mild to moderate head pain.
  • Loss of appetite: reduced desire to eat.

Serious or Rare Side Effects

  • Pulmonary toxicity: interstitial lung disease or fibrosis requiring medical attention.
  • Hepatic injury: elevated liver enzymes or hepatitis.
  • Peripheral neuropathy: tingling or numbness in extremities, especially with prolonged use.

Precautions & Warnings

  • When prescribing Nitrofurantoin, consider the following precautions to ensure safe use.
  • Renal function assessment: evaluate creatinine clearance before initiating therapy.
  • G6PD deficiency: avoid use in patients with known glucose‑6‑phosphate dehydrogenase deficiency.
  • Pregnancy safety: category B; use only if clearly needed during pregnancy.
  • Duration of therapy: limit to the shortest effective course to reduce risk of toxicity.
  • Monitoring for pulmonary symptoms: discontinue if signs of lung irritation develop.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protected from moisture.

Avoid Interactions

Nitrofurantoin can interact with several medicines; some require avoidance while others need careful monitoring.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce nitrofurantoin absorption.
  • Probenecid: decreases renal excretion, increasing plasma levels.
  • Methenamine: concurrent use may diminish antibacterial efficacy.
  • Warfarin: nitrofurantoin can potentiate anticoagulant effect, increasing INR.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: may reduce effectiveness, consider alternative contraception.
  • Vitamin C supplements: increased urinary acidity can affect drug stability.
  • Diuretics: may increase risk of crystalluria, monitor renal function.

Frequently Asked Questions

Nitrofurantoin Manx Healthcare is indicated for the treatment of uncomplicated urinary tract infections (cystitis) caused by susceptible bacteria. It may also be prescribed as a prophylactic agent to reduce the recurrence of urinary tract infections in patients with a history of repeated episodes.

Nitrofurantoin penetrates bacterial cells and interferes with enzymes involved in carbohydrate metabolism, especially those of the electron transport chain. This disruption hampers nucleic acid and protein synthesis, leading to bacterial cell death, primarily against common uropathogens such as Escherichia coli.

The prescribed dose of Nitrofurantoin Manx Healthcare is determined by the treating clinician based on the severity of infection, renal function, and patient-specific factors. Dosage regimens are individualized and should follow the prescriber’s instructions and local clinical guidelines.

Nitrofurantoin is classified as pregnancy category B, indicating that it is generally considered safe when the potential benefit justifies the potential risk to the fetus. Limited data are available for breastfeeding; small amounts may be excreted in milk, so use should be discussed with a healthcare professional.

To place an order, 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 before providing pricing, availability, shipping details and any necessary import documentation.

The most common alternative for uncomplicated UTIs is trimethoprim‑sulfamethoxazole. Nitrofurantoin offers a narrower spectrum focused on urinary pathogens and achieves high urinary concentrations, which can be advantageous in areas with high resistance to trimethoprim‑sulfamethoxazole. However, renal function and potential pulmonary toxicity are specific considerations for nitrofurantoin.

Store Nitrofurantoin Manx Healthcare at ambient temperature, preferably below 25 °C. Keep the tablets in their original packaging, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

The medication is taken orally as a tablet with a full glass of water. It may be taken with or without food, but consistent administration with respect to meals helps maintain stable absorption. Patients should follow the dosing schedule prescribed by their healthcare provider.

Serious adverse events include pulmonary toxicity (interstitial lung disease or fibrosis), hepatic injury (hepatitis or elevated liver enzymes), peripheral neuropathy, and hemolytic anemia in individuals with glucose‑6‑phosphate dehydrogenase deficiency. Prompt medical attention is required if any of these symptoms develop.

Nitrofurantoin should be avoided in patients with severe renal impairment (creatinine clearance <30 mL/min), known hypersensitivity to nitrofurantoin, G6PD deficiency, or a history of nitrofurantoin‑induced pulmonary or hepatic reactions. Caution is also advised for pregnant women, who should only use it when clearly indicated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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