GNH USA

Europe — EMA

Nitrofurantoin Olikla

GNH USA supplies Nitrofurantoin Olikla (Nitrofurantoin), a nitrofuran antibiotic for uncomplicated urinary tract infections.

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What is Nitrofurantoin?

Nitrofurantoin, the active ingredient in Nitrofurantoin Olikla, is a nitrofuran antibiotic presented as an oral tablet for oral use. It treats uncomplicated urinary tract infections in adult patients. GNH USA supplies Nitrofurantoin Olikla as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Nitrofurantoin used for?

Nitrofurantoin is used to manage infections of the urinary tract caused by susceptible bacteria. - Uncomplicated urinary tract infection: eradicates the causative uropathogen and relieves urinary symptoms. - Acute cystitis: provides bacteriostatic or bactericidal activity to clear bladder infection. - Prophylaxis of recurrent urinary tract infection: reduces the frequency of future episodes when taken as a preventive regimen.

What are the side effects of Nitrofurantoin?

Nitrofurantoin may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects: - Nausea: mild to moderate upset stomach. - Loss of appetite: reduced desire to eat. - Headache: transient cranial discomfort. - Diarrhoea: loose stools occurring during therapy.

Serious or Rare Side Effects: - Pulmonary toxicity: interstitial lung disease presenting with cough and dyspnoea. - Hepatic injury: elevated liver enzymes or jaundice. - Peripheral neuropathy: tingling or numbness in extremities. - Hemolytic anaemia: especially in patients with G6PD deficiency. - Severe allergic reactions: rash, angioedema, or anaphylaxis. - Blood dyscrasias: agranulocytosis or leukopenia.

What precautions apply to Nitrofurantoin?

Before prescribing Nitrofurantoin, clinicians should evaluate patient‑specific risk factors and monitor for adverse events. - Renal function assessment: avoid use when creatinine clearance is below 60 mL/min. - G6PD deficiency: use with caution due to risk of haemolysis. - Pulmonary monitoring: discontinue if signs of lung toxicity develop. - Pregnancy and lactation: consider alternative agents unless benefits outweigh risks. - Drug‑induced liver injury: monitor liver function tests during prolonged therapy. - Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

What does Nitrofurantoin interact with?

Nitrofurantoin can interact with several medicines, altering its absorption or increasing toxicity.

Major Interactions (Avoid): - Antacids containing magnesium or aluminium: reduce oral absorption of nitrofurantoin. - Probenecid: increases plasma concentrations, raising risk of toxicity. - Warfarin: may enhance anticoagulant effect, requiring INR monitoring. - Methenamine: concurrent use can diminish antimicrobial efficacy.

Moderate Interactions (Monitor Closely): - Diuretics: may increase nitrofurantoin serum levels, necessitating renal monitoring. - NSAIDs: combined renal stress may impair kidney function. - Oral contraceptives: possible reduction in contraceptive effectiveness, advise additional protection.

Frequently asked questions

What is Nitrofurantoin Olikla used for?+
Nitrofurantoin Olikla is an oral nitrofuran antibiotic indicated for the treatment of uncomplicated urinary tract infections caused by susceptible bacteria, as well as for prophylaxis of recurrent infections in adult patients.
How does nitrofurantoin work?+
Nitrofurantoin is reduced by bacterial enzymes to reactive intermediates that damage bacterial DNA, ribosomal proteins, and cell‑wall components, thereby inhibiting carbohydrate metabolism and interfering with cell‑wall synthesis, which leads to bacteriostatic or bactericidal activity against urinary pathogens.
What is the usual dose of Nitrofurantoin Olikla?+
The dosage regimen for Nitrofurantoin Olikla is determined by the prescribing healthcare professional based on the patient’s condition, renal function, and local treatment guidelines. Patients should follow the prescriber’s instructions precisely.
Is Nitrofurantoin Olikla safe during pregnancy or breastfeeding?+
Safety data for Nitrofurantoin Olikla in pregnancy and lactation are limited. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and alternative agents are preferred when possible.
How do I order Nitrofurantoin Olikla from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does Nitrofurantoin compare with other urinary antiseptics?+
Compared with agents such as trimethoprim‑sulfamethoxazole, nitrofurantoin has a narrow spectrum focused on common uropathogens and is less likely to promote resistance. It is contraindicated in patients with reduced renal function, whereas some alternatives may be used in a broader range of renal capacities.
What are the storage and handling requirements for Nitrofurantoin Olikla?+
Nitrofurantoin Olikla tablets should be stored at temperatures below 25 °C, in the original container, protected from moisture and direct sunlight. Do not store in a bathroom or near a heat source.
How is Nitrofurantoin Olikla administered?+
The medication is taken orally, usually with food or a full glass of water to minimise gastrointestinal irritation. The exact timing and frequency should follow the prescriber’s directions.
What are the most serious risks associated with Nitrofurantoin Olikla?+
Serious adverse events include pulmonary toxicity, hepatic injury, peripheral neuropathy, hemolytic anemia in patients with G6PD deficiency, and severe allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience respiratory symptoms, jaundice, numbness, or signs of an allergic response.
Who should not use Nitrofurantoin Olikla?+
Nitrofurantoin Olikla is contraindicated in patients with severe renal impairment (creatinine clearance <60 mL/min), known hypersensitivity to nitrofurantoin, or a history of pulmonary or hepatic reactions to the drug. Caution is also advised for individuals with G6PD deficiency.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Nitrofurantoin
Route
Oral Use
Manufacturer
Olikla S.R.O.
Origin
EU

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