Amoxicillin Sugar Free Suspension 250 mg/5 ml 100 ml

Amoxicillin Sugar Free Suspension 250 mg/5 ml 100 ml

Amoxicillin

Prescription-only medicine (antibiotic)
  • Licensed UK medicinal product under MHRA (POM) – sugar Free oral suspension authorised for dispensing.
  • Manufactured in compliance with Good Manufacturing Practice (GMP) standards and distributed via authorised UK wholesalers/pharmacies under regulatory oversight.
Oral suspension (sugar-free) amoxicillin

Description

Amoxicillin Sugar-Free Suspension (250 mg/5 ml) is a prescription-only oral antibiotic suspension for wide use. Once reconstituted, each 5 ml dose contains 250 mg of amoxicillin (as amoxicillin trihydrate). The sugar-free formulation is designed for patients who require or prefer a sugar-free liquid antibiotic and for those unable to swallow tablets or capsules. It is indicated for the treatment of a broad spectrum of susceptible bacterial infections including respiratory, urinary, skin and soft tissue, ENT, and dental infections.

Bnefits

  • Sugar-free formulation — suitable for patients needing sugar-free medication (e.g. diabetic patients, sugar-restricted diets)
  • Liquid suspension allows easier administration for children and adults unable to swallow tablets or capsules
  • Broad-spectrum antibiotic effective against many common bacterial pathogens (when susceptible) including those causing ENT, respiratory, urinary, skin, soft tissue and dental infections
  • Flexible dosing based on weight/age or clinical need when prescribed by a qualified clinician
  • Well-established safety profile and extensive clinical usage history for a range of bacterial infections globally

Indications

  • Acute bacterial sinusitis, acute otitis media, acute streptococcal tonsillitis and pharyngitis
  • Lower respiratory tract infections including acute exacerbations of chronic bronchitis and community-acquired pneumonia when caused by susceptible organisms
  • Urinary tract infections including acute cystitis and pyelonephritis (in susceptible cases)
  • Skin and soft tissue infections including wound infections and cellulitis (when caused by susceptible bacteria)
  • Dental infections including dental abscesses, especially with spreading cellulitis or in combination with dental procedures
  • Prophylaxis of bacterial endocarditis and prophylaxis before certain procedures where indicated (in susceptible patients)

Composition

  • Amoxicillin trihydrate BP equivalent to 250 mg amoxicillin per 5 ml dose of reconstituted suspension
  • Excipients include sorbitol (E420) as sweetener in sugar-free formulation, sodium benzoate (E211) preservative, sodium citrate, citric acid, flavouring agents (e.g. banana flavour), colloidal anhydrous silica, xanthan gum and other standard suspension excipients, depending on manufacturer batch.
  • Free from sucrose (sugar-free), making it suitable for patients with sugar intake restrictions.

Formulation

  • Powder for oral suspension (sugar-free) to be reconstituted with water to obtain 100 ml suspension.
  • Oral antibiotic (beta-lactam aminopenicillin) intended for systemic antibacterial therapy when taken orally.

Packaging

  • Bottle of 100 ml powder for oral suspension (unreconstituted) per pack (POM x1) as supplied in UK pharmacies/wholesalers.
  • Outer carton with patient information leaflet (PIL) and instructions for reconstitution and use.

Usage

  • Dispensed and reconstituted by a pharmacist according to the manufacturer’s instructions before first use.
  • Shake well before each dose to ensure uniform suspension.
  • Dosing to be determined by prescriber based on infection type, patient’s age/weight and renal function. Commonly given 3 times daily (every 8 hours) or as per prescription.
  • Give with or without food; taking with food may reduce gastrointestinal upset in some patients.
  • Use an oral syringe or medicine spoon for accurate measurement; do not use a kitchen teaspoon.
  • Complete full prescribed course even if symptoms improve earlier, to avoid relapse or antibiotic resistance.

Contraindications

  • Known hypersensitivity to amoxicillin, any penicillin or any component of the formulation (including sorbitol or preservatives)
  • History of severe immediate hypersensitivity reaction (e.g. anaphylaxis or angioedema) to beta-lactam antibiotics such as penicillins or cephalosporins.
  • Patients with hereditary fructose intolerance or other known intolerance to sorbitol (excipients), as sugar-free formulation contains sorbitol E420.
  • Infections caused by bacteria resistant to amoxicillin; use only when susceptibility is confirmed or strongly suspected.
  • Severe renal impairment may require dose adjustment; prescriber must evaluate renal function.

Adverse Effects

  • Common: nausea, vomiting, diarrhoea, abdominal discomfort.
  • Skin reactions: rash, urticaria, possible allergic reactions.
  • Rare but serious: severe allergic reactions including anaphylaxis, angioedema, Stevens–Johnson syndrome or toxic epidermal necrolysis in susceptible individuals.
  • Possible overgrowth of non-susceptible organisms (e.g. Candida) or altered gut flora, especially during prolonged use.
  • Potential liver enzyme changes or hepatic disturbances (rare), reversible upon discontinuation.
  • Risk of Clostridioides difficile–associated diarrhoea/colitis, particularly with extended use or in elderly patients.

Storage Conditions

  • Store powder (unreconstituted) at room temperature (below 25°C) in original bottle until reconstitution.
  • After reconstitution, store as directed by the pharmacist (often fridge 2–8 °C) and use within the period specified on the bottle label (commonly 7–14 days).
  • Keep out of sight and reach of children.
  • Do not use after expiry date printed on the packaging or if the bottle or contents appear damaged or contaminated.

Duration

Depends on the type and severity of infection; durations commonly range from 5 to 10 days for common infections, but may be longer as per prescriber\u2019s recommendation.

Onset

Symptomatic improvement often begins within a few days (e.g. 2\u20133 days), but full benefit and eradication of bacteria require completion of full treatment course.

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