Broad-spectrum antibiotic
  • AUGMIT® is a broad spectrum combination of Amoxicillin and the β-lactamase inhibitor, Clavulanate potassium. 
  • AUGMIT® exhibits bactericidal activity against many Gram-positive and Gram-negative organisms: Staphylococcus aureus (β-lactamase and non-β-lactamase producing),Streptococcus species, Enterobacter species, E. coli, Haemophilus influenzae, Klebsiella species, Moraxella catarrhalis and Clostridium species. 
  •  Amoxicillin and Clavulanate potassium are well absorbed from the gastrointestinal tract.  
  • AUGMIT® can be given without regard to meals.

Each 5 ml of AUGMIT® 312 for Oral suspension contains:

  • Amoxicillin 250 mg (as Amoxicillin Trihydrate)
  • Clavulanic acid 62.5 mg (as Potassium salt)

AUGMIT® is indicated in the following infections caused by susceptible organisms: 

  • Upper respiratory tract infections (including ENT) e.g. recurrent tonsillitis, sinusitis, otitis media. 
  • Lower respiratory tract infections e.g. acute and chronic bronchitis, lobar and bronchopneumonia. 
  • Genito-urinary tract infections e.g. cystitis, urethritis, pyelonephritis.
  • Skin and soft tissue infections.  
  • Other infections: bone and joint infections, dental infections and intra-abdominal sepsis.

AUGMIT® is contraindicated in patients with a history of allergic reactions to any penicillin. It is also contraindicated in patients with a previous history of AUGMIT® or penicillin-associated jaundice/hepatic dysfunction. 

  • AUGMIT® should be used with care in patients on anti-coagulation therapy.
  •  It may reduce the efficacy of oral contraceptives.
  • Concomitant use of probenecid with AUGMIT® may result in increased and prolonged blood levels of Amoxicillin but not Clavulanic acid.
  • Concomitant use AUGMIT® with Allopurinol can increase the likelihood of allergic skin reactions, due to containing Amoxicillin. 
  • AUGMIT® have shown no teratogenic effect.
  • As with all medicines use should be avoided in pregnancy especially during the first trimester unless considered essential by the physician. 
  • AUGMIT® may be administered during the period of lactation.
  • Gastrointestinal reaction:                                       -  Effects include diarrhoea, indigestion, nausea and vomiting, candidiasis, antibiotic-associated colitis have been reported rarely.                               - Tooth discolouration has been reported rarely, mostly with the suspension. It can usually be removed by brushing.
  • Hepatic effects: A moderate rise in AST and/or ALT has been noted in patients with semi-synthetic penicillins but the significance of these findings is unknown. Hepatitis and cholestatic jaundice have been reported rarely.
  • Hypersensitivity reactions:Urticarial and erythematous rashes sometimes occur. Rarely erythema multiform, Stevens-Johnson syndrome, toxic epidermal necrolysis, bullous exfoliative dermatitis.
  • Hematological effects:As with other ß-lactam reversible leucopenia (including neutropenia or agranulocytosis) reversible thrombocytopenia and heamolytic anaemia have been reported rarely.
  • CNS effects :CNS effects have been seen very rarely. These include reversible hyperactivity, dizziness, headache and convulsions. Convulsions may occur with impaired renal function or in those receiving high dose. 

Over dose:-

  • Cases of over dosage with AUGMIT® are usually symptomatic. If encountered,  gastrointestinal symptoms and disturbance of the fluid and electrolyte balances my be evident. They may be treated symptomatically, with attention to the water/ electrolyte balance. AUGMIT® may be removed from the circulation by hemodialysis.

1) Children:

Patients aged 1 years and older-
:In mild to moderate infections

  •    1-6 years: 2.5 ml three times daily.
  •    7-12 years: 5 ml three times daily.

In sever infection: 

  •    1-6 years: 5 ml three times daily.
  •    7-12 years: 10 ml three times daily.

2) Infants:

 Augmit should be used in neonates and infants aged less than 12 weeks  (3 months ) as :-             

  • 30mg/kg/day divided into 2 doses.    
  • 20mg/kg/day divided into 3 doses.

 In more serious infections ,the dosage may be increased up to 50 mg/kg/day divided into 3 doses

* Treatment should not be extended beyond 14 days without review to the physician.
* Pediatric patients weighing 40 kg and more should be dosed according to the adult.
* Dosage in renal impairment should be reduced.



  • AUGMIT® should be used with caution in patients with hepatic dysfunction and renal impairment.
  • The possibility of superinfections with mycotic or bacterial pathogens should be kept in mind during therapy. If superinfections occur, the drug should be discontinued and appropriate therapy instituted.
  • AUGMIT® 375 mg, 625 mg and 1000 mg tablets should not be recommended in children under 12 year.
  • AUGMIT® 1000 mg tablet should only be used in patients with a glomerular filtration rate of > 30 ml/min.
  • AUGMIT® 312 for Oral suspension: Bottle of 100 ml after reconstitution.


  • Store in a dry place at a temperature below 25° C. 
  • AUGMIT® suspension, once reconstituted, must be stored in a refrigerator and used within 7 days.