AUGMENTIN — Co-amoxiclav (Amoxicillin/Clavulanate) 625 mg, 1g tablets
📦 Product Snapshot
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🧠 Overview
Augmentin is the brand name for co-amoxiclav, a fixed‑dose combination antibiotic containing amoxicillin (a penicillin‑class antibiotic) and clavulanate potassium (a beta‑lactamase inhibitor). It was first approved in the US in 1984 and remains one of the most widely prescribed broad‑spectrum antibiotics worldwide. The combination is designed to overcome bacterial resistance mediated by beta‑lactamase enzymes.
Mechanism of action: Amoxicillin kills bacteria by inhibiting the synthesis of bacterial cell walls, leading to cell lysis. However, some bacteria produce beta‑lactamase enzymes that inactivate amoxicillin by breaking open its beta‑lactam ring. Clavulanate has weak antibacterial activity itself but irreversibly binds to beta‑lactamases, protecting amoxicillin from degradation. This extends amoxicillin‘s spectrum to include beta‑lactamase‑producing strains of Haemophilus influenzae, Moraxella catarrhalis, Staphylococcus aureus, Escherichia coli, Klebsiella species, and others.
Clinical indications: Augmentin is indicated for a wide range of community‑acquired infections in adults and children, including lower respiratory tract infections (e.g., community‑acquired pneumonia, bronchitis), acute bacterial otitis media, sinusitis, skin and skin structure infections (e.g., cellulitis, abscesses, wound infections), urinary tract infections, dental abscesses, and bone/joint infections (e.g., osteomyelitis). It is also used for surgical prophylaxis in certain procedures.
Limitations of use: When susceptibility testing shows that the infecting bacteria are susceptible to amoxicillin alone (i.e., they do not produce beta‑lactamase), Augmentin should not be used, as the clavulanate component adds unnecessary risk of hepatotoxicity and gastrointestinal side effects. Augmentin is not effective against viruses (common cold, flu) and should be used only for proven or strongly suspected bacterial infections to reduce the development of drug resistance.
🏷️ Strengths & Brand Examples
- Oral tablets: 250 mg/125 mg, 500 mg/125 mg, 875 mg/125 mg (amoxicillin/clavulanate). Often referred to by total mg: 375 mg, 625 mg, 1 g respectively.
- Chewable tablets: 200 mg/28.5 mg, 400 mg/57 mg.
- Extended‑release tablets (XR): 1000 mg/62.5 mg (for certain infections).
- Oral suspension (powder for reconstitution): 125 mg/31.25 mg per 5 mL, 200 mg/28.5 mg per 5 mL, 250 mg/62.5 mg per 5 mL, 400 mg/57 mg per 5 mL, 600 mg/42.9 mg per 5 mL.
- Intravenous injection: 500 mg/100 mg, 1 g/200 mg vials.
- Augmentin® (GSK) — 250/125, 500/125, 875/125 tablets.
- Augmentin ES-600® — oral suspension 600 mg/42.9 mg per 5 mL.
- Augmentin XR® — extended‑release tablets 1000 mg/62.5 mg.
- Generic versions widely available.
- Augmentin® (GSK) — available as tablets, suspension, IV.
- Co‑amoxiclav (generic name) — widely prescribed under generic names.
- Augmentin 625 Duo® (GlaxoSmithKline Pharmaceuticals Ltd) — amoxicillin 500 mg + clavulanic acid 125 mg tablets.
- Amoxyclav 625® (Alkem Laboratories) — one of the most prescribed generics.
- Almox-CV 625® (Alkem) — amoxicillin 500 mg + clavulanate 125 mg.
- Moxclav 625® (Sun Pharma) — available in tablets and suspension.
- Clavam 625® (Cipla) — tablets and dry syrup.
- Other manufacturers: Zydus Cadila (Clavix 625), Torrent (Clavulin), Intas (Clavicip), Abbott (Moxikind-CV), Healing Pharma (Amoxyheal CV).
- Injections: Augmentin 1.2 gm IV (GSK), Clavam 1.2 gm (Alkem), various generics.
⚠️ Safety, Side Effects & Monitoring
- Diarrhea or loose stools (most common, 9%) — may be severe or persistent.
- Nausea (3%), vomiting (1%).
- Skin rash and urticaria (3%).
- Vaginal itching or discharge (vaginitis, 1%).
- Diaper rash (in children).
- Thrush (oral or vaginal fungal overgrowth).
- Indigestion, abdominal discomfort.
• Severe cutaneous adverse reactions (SCAR): Stevens‑Johnson Syndrome (SJS), Toxic Epidermal Necrolysis (TEN), Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS), and Acute Generalized Exanthematous Pustulosis (AGEP) reported. Discontinue at first sign of skin rash, blistering, or mucosal lesions.
• Hepatic dysfunction (boxed‑level warning): Cholestatic jaundice and hepatitis reported, more common in males, elderly, and with prolonged use. Onset may be delayed up to 6 weeks after treatment. Contraindicated in patients with history of Augmentin‑associated jaundice or hepatic dysfunction. Monitor liver function tests in patients with pre‑existing liver disease. Discontinue if symptoms of liver injury (right upper quadrant pain, dark urine, pale stools, yellowing of skin/eyes).
• Clostridioides difficile‑associated diarrhea (CDAD): Reported with all antibiotics, severity from mild diarrhea to fatal colitis. Evaluate if diarrhea occurs during or after treatment (even months later). Do not use anti‑diarrhea drugs that slow motility.
• Drug‑induced enterocolitis syndrome (DIES): Rare but serious reaction with severe vomiting, diarrhea, hypotension, and pallor within hours of dosing. Discontinue immediately.
• Rash in mononucleosis: High incidence of rash (up to 90%) in patients with infectious mononucleosis. Avoid Augmentin in suspected mono.
• Microbial overgrowth: Prolonged use may result in superinfection with resistant bacteria or fungi (Candida).
• Bleeding abnormalities: Rarely, prolonged prothrombin time reported with penicillins. Monitor if on anticoagulants.
• Renal impairment: Dose adjustment required in severe renal impairment (GFR less than 30 mL/min). Extended‑release tablets not recommended in severe renal impairment.
• Phenylketonuria (PKU): Chewable tablets and oral suspension may contain phenylalanine. Check product labeling.
- History of a serious hypersensitivity reaction (e.g., anaphylaxis) to amoxicillin, clavulanate, any penicillin, or other beta‑lactam antibiotics (cephalosporins, carbapenems).
- History of cholestatic jaundice or hepatic dysfunction associated with Augmentin use.
- Known hypersensitivity to any component of the formulation.
- Do not use when amoxicillin alone is effective (i.e., infections caused by bacteria not producing beta‑lactamase).
- Probenecid: Decreases renal tubular secretion of amoxicillin, increasing and prolonging amoxicillin blood levels. Not recommended.
- Oral anticoagulants (warfarin): May increase INR and bleeding risk. Monitor coagulation parameters closely.
- Allopurinol: Concomitant use increases risk of rash.
- Oral contraceptives: Amoxicillin/clavulanate may reduce efficacy of hormonal contraceptives. Advise patients to use additional non‑hormonal contraception (condoms, diaphragm) during treatment and for 7 days after stopping.
- Methotrexate: Penicillins may reduce methotrexate clearance, increasing toxicity risk. Monitor methotrexate levels.
- Mycophenolate mofetil: Amoxicillin/clavulanate may reduce mycophenolic acid concentrations. Monitor for reduced efficacy.
- Tetracyclines, macrolides, chloramphenicol: Bacteriostatic antibiotics may antagonize bactericidal action of penicillins. Avoid concurrent use.
- Pregnancy: Generally considered safe. Animal studies do not indicate direct or indirect harmful effects. Use if clearly needed.
- Breastfeeding: Amoxicillin and clavulanate are excreted in breast milk in small amounts. Considered compatible with breastfeeding; monitor infant for diarrhea, rash, or thrush.
- Pediatric use: Safety established. Dosing based on weight and age. Neonates and infants less than 12 weeks: 30 mg/kg/day divided every 12 hours (based on amoxicillin). Children 12 weeks and older: 25‑45 mg/kg/day every 12 hours or 20‑40 mg/kg/day every 8 hours. Do not exceed adult dose.
- Geriatric use: No specific problems demonstrated, but elderly more likely to have age‑related renal impairment; dose adjustment may be needed. Increased risk of hepatotoxicity.
- Renal impairment: GFR 10‑30 mL/min: 250‑500 mg every 12 hours (based on amoxicillin). GFR less than 10 mL/min: 250‑500 mg every 24 hours. Hemodialysis: 250‑500 mg during dialysis and after. Extended‑release tablets contraindicated in severe renal impairment.
- Hepatic impairment: Use with caution; monitor liver function tests. Contraindicated in history of Augmentin‑associated jaundice/hepatic dysfunction.
- Symptoms: Nausea, vomiting, diarrhea, stomach pain, skin rash, drowsiness, hyperactivity, decreased urination. Crystalluria possible with high doses.
- Management: Supportive care, fluid monitoring, correction of electrolyte imbalances. Activated charcoal may be considered if recent ingestion. Hemodialysis removes amoxicillin/clavulanate.
❓ FAQ
📚 Official References
- DailyMed — AUGMENTIN (amoxicillin and clavulanate potassium) for suspension full prescribing information
- Drugs.com — Amoxicillin and clavulanate potassium patient information
- WebMD — Amoxicillin/Clavulanate (Augmentin) uses, side effects, interactions
- 1mg India — Augmentin 625 Duo Tablet (consumer information)
- Pharmacy2U UK — Co-amoxiclav patient information