Product image of Interfos Adulti (Fosfomycin Trometamol) supplied by GNH India

Interfos Adulti

Active Ingredient:
Fosfomycin Trometamol
Origin:
EU

Interfos Adulti (Fosfomycin Trometamol)

Fosfomycin Trometamol, the active ingredient in Interfos Adulti, is a phosphonic acid antibiotic presented as an oral dosage form for oral use. It treats uncomplicated urinary tract infections in adult patients and is indicated for a single‑dose oral regimen that provides high urinary concentrations and is effective against a broad range of uropathogens.

GNH India supplies Interfos Adulti as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, adhering to stringent quality standards and regulatory requirements to ensure product integrity.

Manufacturer / TM Owner

Pharmextracta S.P.A

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Indications & Clinical Uses

Fosfomycin Trometamol is used to treat bacterial infections of the urinary tract.

  • Uncomplicated urinary tract infections: eliminates the causative bacteria and resolves urinary symptoms.
  • Acute uncomplicated cystitis: provides a single oral dose that clears infection in most patients.
  • Susceptible uropathogen infections: offers high urinary concentrations that achieve bactericidal activity.

How It Works

  • Fosfomycin Trometamol exerts its antibacterial effect by irreversibly inhibiting the enzyme MurA (enolpyruvyl transferase), a key catalyst in the early stage of peptidoglycan synthesis. By blocking the formation of N‑acetylmuramic acid, the drug prevents construction of the bacterial cell wall, leading to cell lysis and death of susceptible Gram‑positive and Gram‑negative organisms. This mechanism is independent of common resistance pathways and results in rapid bactericidal activity.

Side Effects

Fosfomycin Trometamol may cause adverse reactions, ranging from mild to severe.

Common Side Effects

  • Nausea: mild stomach upset that may resolve without treatment.
  • Diarrhea: loose stools occurring during or after therapy.
  • Headache: transient head discomfort.
  • Abdominal pain: cramping or discomfort in the stomach area.
  • Flatulence: increased intestinal gas.
  • Taste disturbance: altered taste perception.

Serious or Rare Side Effects

  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Clostridioides difficile infection: severe colitis following antibiotic use.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Renal impairment: worsening kidney function in susceptible patients.
  • Anaphylaxis: life‑threatening systemic allergic response.

Precautions & Warnings

When prescribing Fosfomycin Trometamol, clinicians should consider several precautionary measures to ensure safe use.

  • Renal function assessment: evaluate creatinine clearance before initiating therapy.
  • Pregnancy safety: use only if potential benefit justifies the risk, as data are limited.
  • Breastfeeding: assess risk versus benefit, as excretion in milk is possible.
  • Known hypersensitivity: avoid in patients with previous allergic reactions to fosfomycin.
  • Concomitant nephrotoxic drugs: monitor renal function if used together.
  • Drug interactions: review patient medication list for potential interactions.
  • Store at below 25°C: keep in the original packaging, protect from moisture and heat.

Avoid Interactions

Fosfomycin Trometamol can interact with other medicines, affecting its absorption or activity.

Major Interactions (Avoid)

  • Antacids containing magnesium or aluminum: reduce fosfomycin absorption; separate dosing by at least 2 hours.
  • Metoclopramide or other pro‑kinetic agents: delay gastric emptying and lower drug exposure.
  • Co‑administration with other nephrotoxic agents: may increase risk of renal toxicity.

Moderate Interactions (Monitor Closely)

  • Warfarin: fosfomycin may potentiate anticoagulant effect; monitor INR.
  • Oral contraceptives: possible reduction in efficacy; advise additional contraceptive measures.
  • Diuretics: may alter renal excretion of fosfomycin; monitor fluid and electrolyte balance.

Frequently Asked Questions

Interfos Adulti contains fosfomycin trometamol and is indicated for the treatment of uncomplicated urinary tract infections in adult patients. It is typically prescribed as a single oral dose that provides high concentrations of the drug in the urine to eradicate the causative bacteria.

Fosfomycin trometamol works by irreversibly inhibiting the bacterial enzyme MurA, which is essential for the early steps of peptidoglycan synthesis. By blocking this pathway, the drug prevents formation of the bacterial cell wall, leading to cell lysis and death of susceptible organisms.

The dosage of Interfos Adulti is determined by the prescribing healthcare professional based on the patient’s clinical condition, renal function, and local treatment guidelines. Patients should follow the prescriber’s instructions and not alter the dose on their own.

Safety data for fosfomycin trometamol in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss use with their healthcare provider.

To request Interfos Adulti, 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.

Compared with commonly used agents such as nitrofurantoin or trimethoprim‑sulfamethoxazole, fosfomycin offers a single‑dose regimen and retains activity against many multidrug‑resistant uropathogens. However, local resistance patterns and patient-specific factors should guide the choice of therapy.

Interfos Adulti should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight. Keeping the product in a dry, cool environment helps maintain its stability and potency throughout its shelf life.

Interfos Adulti is taken orally, usually as a single dose taken with a full glass of water. The tablet should be swallowed whole and not chewed or crushed, unless otherwise directed by a healthcare professional.

Serious adverse events, although rare, include severe allergic reactions such as anaphylaxis, Stevens‑Johnson syndrome, toxic epidermal necrolysis, Clostridioides difficile‑associated colitis, hepatic dysfunction, and worsening renal impairment. Patients should seek immediate medical attention if they experience any of these symptoms.

Interfos Adulti is contraindicated in individuals with a known hypersensitivity to fosfomycin or any component of the formulation. Caution is also advised for patients with severe renal impairment, as dose adjustment may be required, and for those taking medications that may interact significantly with fosfomycin.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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