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Beta-lactam / Beta-lactamase inhibitor combination antibiotic Pregnancy: §4.6 Pregnancy: 'Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/foetal development, parturition or postnatal development… Limited data on the use of amoxicillin/clavulanic acid during pregnancy in humans do not indicate an increased risk of congenital malformations. In a single study in women with preterm, premature rupture of the foetal membrane it was reported that prophylactic treatment with amoxicillin/clavulanic acid may be associated with an increased risk of necrotising enterocolitis in neonates. Use should be avoided during pregnancy, unless considered essential by the physician.' Breast-feeding: 'Both substances are excreted into breast milk (nothing is known of the effects of clavulanic acid on the breast-fed infant). Consequently, diarrhoea and fungus infection of the mucous membranes are possible in the breast-fed infant, so that breast-feeding might have to be discontinued. The possibility of sensitisation should be taken into account. Amoxicillin/clavulanic acid should only be used during breast-feeding after benefit/risk assessment by the physician in charge.'

Co-amoxiclav 625mg (COPD Exacerbation / CAP)

Brand names: Augmentin (500/125 mg tablets), Co-amoxiclav (generic)

This is co-amoxiclav, a combination of amoxicillin with the beta-lactamase inhibitor clavulanic acid, used here for COPD exacerbations and community-acquired pneumonia where broader cover is needed. It is typically reserved for more severe presentations or where first-line narrower agents are unsuitable.

Adult dose

Dose: One 500 mg/125 mg dose (amoxicillin 500 mg + clavulanic acid 125 mg = one 625 mg tablet)
Route: Oral
Frequency: Three times a day
Max: 1500 mg amoxicillin + 375 mg clavulanic acid per day (three 500 mg/125 mg doses) — 'For adults and children ≥ 40 kg, this formulation of Augmentin provides a total daily dose of 1500 mg amoxicillin/375 mg clavulanic acid, when administered as recommended below.'; if more amoxicillin is required the SPC directs the prescriber to a different Augmentin preparation rather than to a higher dose of this one.
SCOPE: the fetched §4.2 gives ONE general adult regimen for this product and does not break dosing down by indication; §4.1 (therapeutic indications) was not part of the fetched bundle, so this SPC neither confirms nor excludes the specific respiratory indications named on the page (acute exacerbation of COPD, community-acquired pneumonia, aspiration pneumonia) — those, the choice between amoxicillin and co-amoxiclav, and course lengths must come from a UK guideline such as NICE. What is published above is the SPC's general adult dose for this exact product, which is the dose the page is built around. Verbatim posology: 'Adults and children ≥ 40 kg — One 500 mg/125 mg dose taken three times a day.' Both components of the fixed combination are quantified (amoxicillin 500 mg + clavulanic acid 125 mg = the page's 625 mg tablet). Doses 'are expressed throughout in terms of amoxicillin/clavulanic acid content'. DURATION: no course length is published above because the SPC does not give one — 'The duration of therapy should be determined by the response of the patient. Some infections (e.g. osteomyelitis) require longer periods of treatment. Treatment should not be extended beyond 14 days without review.' ADMINISTRATION: 'Augmentin is for oral use. Augmentin should be administered with a meal to minimise potential gastrointestinal intolerance. Therapy can be started parenterally according to the SmPC of the IV formulation and continued with an oral preparation.' Elderly: 'No dose adjustment is considered necessary.' Choice of dose: 'The dose of Augmentin that is selected to treat an individual infection should take into account: • The expected pathogens and their likely susceptibility to antibacterial agents (see section 4.4) • The severity and the site of the infection • The age, weight and renal function of the patient as shown below.' If a higher amoxicillin dose is needed, 'it is recommended that another preparation of Augmentin is selected in order to avoid administration of unnecessarily high daily doses of clavulanic acid'. De-escalation (§4.4): 'In the case that an infection is proven to be due to an amoxicillin-susceptible organisms(s) then consideration should be given to switching from amoxicillin/clavulanic acid to amoxicillin in accordance with official guidance.'

Paediatric dose

Route: Oral
Frequency: Given in three divided doses
Max: 2400 mg amoxicillin / 600 mg clavulanic acid daily — 'For children < 40 kg, this formulation of Augmentin provides a maximum daily dose of 2400 mg amoxicillin/600 mg clavulanic acid, when administered as recommended below.' (§4.2)
dosePerKg is deliberately NULL: the SPC gives a RANGE, not a single per-dose figure — 'Children < 40 kg 20 mg/5 mg/kg/day to 60 mg/15 mg/kg/day given in three divided doses' (expressed per day, and as amoxicillin/clavulanic acid). Choosing any single point value from that range would not be verbatim, so the regimen is left in prose for the prescriber. TABLET RESTRICTIONS (§4.2): 'As the tablets cannot be divided, children weighing less than 25 kg must not be treated with Augmentin tablets'; 'Children aged 6 years and below or weighing less than 25 kg should preferably be treated with Augmentin suspension or paediatric sachets.' The SPC's worked table for a single 500/125 mg tablet gives amoxicillin per single dose of 12.5 mg/kg at 40 kg, 14.3 mg/kg at 35 kg, 16.7 mg/kg at 30 kg and 20.0 mg/kg at 25 kg (clavulanic acid 3.1, 3.6, 4.2 and 5.0 mg/kg respectively) — i.e. weight-banded for the tablet, which is why no single per-kg value is set. 'No clinical data are available on doses of Augmentin 4:1 formulations higher than 40 mg/10 mg/kg per day in children under 2 years.' Children weighing 40 kg or more take the adult regimen (one 500 mg/125 mg dose three times a day). concentration is NULL because this SPC is for a tablet and the bundle contains no UK suspension strength; the only suspension strength in the bundle (600 mg/42.9 mg per 5 mL) is a US product that does not correspond to this UK page, so it must not be used to compute a volume here.

Dose adjustments

Renal

§4.2 Renal impairment (dose adjustments are based on the maximum recommended level of amoxicillin): 'No adjustment in dose is required in patients with creatinine clearance (CrCl) greater than 30 ml/min.' Adults and children weighing 40 kg or more — CrCl 10-30 ml/min: '500 mg/125 mg twice daily'; CrCl < 10 ml/min: '500 mg/125 mg once daily'; haemodialysis: '500 mg/125 mg every 24 hours, plus 500 mg/125 mg during dialysis, to be repeated at the end of dialysis (as serum concentrations of both amoxicillin and clavulanic acid are decreased)'. Children under 40 kg — CrCl 10-30 ml/min: '15 mg/3.75 mg/kg twice daily (maximum 500 mg/125 mg twice daily)'; CrCl < 10 ml/min: '15 mg/3.75 mg/kg as a single daily dose (maximum 500 mg/125 mg)'; haemodialysis: '15 mg/3.75 mg/kg per day once daily. Prior to haemodialysis 15 mg/3.75 mg/kg. In order to restore circulating drug levels, 15 mg/3.75 mg per kg should be administered after haemodialysis.' §4.4 also notes convulsions may occur in patients with impaired renal function.

Hepatic

§4.2 Hepatic impairment: 'Dose with caution and monitor hepatic function at regular intervals (see sections 4.3 and 4.4).' No numeric reduction is given. Note the §4.3 contraindication: 'History of jaundice/hepatic impairment due to amoxicillin/clavulanic acid'. US label §2.4 agrees: 'Hepatically impaired patients should be dosed with caution and hepatic function monitored at regular intervals'.

Dose independently re-sourced from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — clinician-reviewed. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to the active substances, to any of the penicillins or to any of the excipients listed in section 6.1 (§4.3)
  • History of a severe immediate hypersensitivity reaction (e.g. anaphylaxis) to another beta-lactam agent (e.g. a cephalosporin, carbapenem or monobactam) (§4.3)
  • History of jaundice/hepatic impairment due to amoxicillin/clavulanic acid (§4.3)
  • Avoid if infectious mononucleosis is suspected — §4.4: 'Amoxicillin/clavulanic acid should be avoided if infectious mononucleosis is suspected since the occurrence of a morbilliform rash has been associated with this condition following the use of amoxicillin' (caution, not a formal §4.3 contraindication)
  • Not for use where reduced susceptibility is not beta-lactamase mediated — §4.4: 'This presentation of Augmentin is not suitable for use when there is a high risk that the presumptive pathogens have reduced susceptibility or resistance to beta-lactam agents that is not mediated by beta-lactamases susceptible to inhibition by clavulanic acid. This presentation should not be used to treat penicillin-resistant S. pneumoniae.'

Side effects

  • Gastrointestinal — diarrhoea: very common (≥1/10). Nausea and vomiting: common. §4.8: 'The most commonly reported adverse drug reactions (ADRs) are diarrhoea, nausea and vomiting'; 'Nausea is more often associated with higher oral doses. If gastrointestinal reactions are evident, they may be reduced by taking amoxicillin/clavulanic acid with a meal'
  • Gastrointestinal — indigestion: uncommon. Frequency not known: antibiotic-associated colitis (including pseudomembranous and haemorrhagic colitis), drug-induced enterocolitis syndrome, acute pancreatitis, black hairy tongue
  • Infections — mucocutaneous candidosis: common; overgrowth of non-susceptible organisms: frequency not known
  • Skin — rash, pruritus and urticaria: uncommon; erythema multiforme: rare; frequency not known: Stevens-Johnson syndrome, toxic epidermal necrolysis, bullous exfoliative dermatitis, acute generalised exanthematous pustulosis (AGEP), DRESS, symmetrical drug-related intertriginous and flexural exanthema (SDRIFE), linear IgA disease
  • Hepatobiliary — rises in AST and/or ALT: uncommon; hepatitis and cholestatic jaundice: frequency not known
  • Blood — reversible leucopenia (including neutropenia) and thrombocytopenia: rare; frequency not known: reversible agranulocytosis, haemolytic anaemia, prolongation of bleeding time and prothrombin time
  • Nervous system — dizziness and headache: uncommon; frequency not known: reversible hyperactivity, convulsions, aseptic meningitis. §4.4: 'Convulsions may occur in patients with impaired renal function or in those receiving high doses'
  • Immune (frequency not known) — angioneurotic oedema, anaphylaxis, serum sickness-like syndrome, hypersensitivity vasculitis, haemophagocytic lymphohistiocytosis (HLH)/macrophage activation syndrome; cardiac: Kounis syndrome. §4.4: 'Hypersensitivity reactions can also progress to Kounis syndrome, a serious allergic reaction that can result in myocardial infarction'
  • Drug-induced enterocolitis syndrome (§4.4): 'reported mainly in children receiving amoxicillin/clavulanic acid… an allergic reaction with the leading symptom of protracted vomiting (1-4 hours after drug administration) in the absence of allergic skin or respiratory symptoms… There have been severe cases including progression to shock'
  • Renal (frequency not known) — interstitial nephritis, crystalluria including acute renal injury
  • This side-effect list may be incomplete — check the full SPC.

Monitoring

  • Hepatic function — §4.2 Hepatic impairment: 'Dose with caution and monitor hepatic function at regular intervals'; US label §5.4: 'Monitor liver function tests in patients with hepatic impairment' and 'Discontinue if signs/symptoms of hepatitis occur'
  • Duration of therapy — §4.2: 'The duration of therapy should be determined by the response of the patient… Treatment should not be extended beyond 14 days without review'
  • Diarrhoea — evaluate for antibiotic-associated / Clostridioides difficile colitis; US label §5.5 lists 'Clostridioides difficile - associated diarrhea (CDAD) (ranging from mild diarrhea to fatal colitis): Evaluate patients if diarrhea occurs.'
  • Rash — US label §5.2 (severe cutaneous adverse reactions): 'Monitor closely. Discontinue if rash progresses'; UK §4.8 footnote: 'If any hypersensitivity dermatitis reaction occurs, treatment should be discontinued'
  • HLH/MAS — §4.4: 'Clinical signs and symptoms of HLH/MAS include fever, rash, neurological symptoms, hepatosplenomegaly, lymphadenopathy, cytopenias, high serum ferritin, hypertriglyceridaemia and abnormalities of liver function and coagulation. Patients who develop these signs and symptoms should be immediately evaluated'
  • INR / prothrombin time when co-prescribed with an oral anticoagulant — US label §7.2: 'Abnormal prolongation of prothrombin time (increased international normalized ratio [INR]) has been reported… Appropriate monitoring should be undertaken when anticoagulants are prescribed concurrently'
  • Renal function informs the dose — §4.2: 'The dose… should take into account… The age, weight and renal function of the patient'

Clinical monograph

How it works

Amoxicillin inhibits bacterial cell-wall synthesis, while clavulanic acid protects it from breakdown by beta-lactamase enzymes, extending activity to many resistant respiratory organisms. The pairing restores efficacy against beta-lactamase-producing strains.

Prescribing in practice

  • Contraindicated in penicillin hypersensitivity and in anyone with a history of co-amoxiclav- or penicillin-associated jaundice or hepatic dysfunction, as the clavulanate component carries a distinct risk of cholestatic liver injury.
  • Use cautiously in significant hepatic impairment and reduce the dose in renal impairment per current prescribing references.
  • Counsel on Clostridioides difficile risk with this broad-spectrum agent and avoid unnecessary use.

Monitoring

Monitor for hepatic effects (especially on longer courses or in older patients), clinical response, and any new diarrhoea suggestive of C. difficile.

Counselling the patient

  • Take with food to reduce stomach upset and complete the course.
  • Report jaundice, dark urine, or persistent watery or bloody diarrhoea.
  • Tell your prescriber about any penicillin or antibiotic allergy.

Evidence & guidelines

NICE guidance on COPD exacerbations and pneumonia lists co-amoxiclav among antibiotic options, generally for more severe disease or when first-line agents are unsuitable.

Reference: NICE NG120 Pneumonia; NICE NG115 COPD; NICE CKS Lower Respiratory Tract Infection; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.