MAXAMOX amoxicillin trihydrate 500mg/5mLpowder for oral suspension bottle Australia - English - Department of Health (Therapeutic Goods Administration)

maxamox amoxicillin trihydrate 500mg/5mlpowder for oral suspension bottle

sandoz pty ltd - amoxicillin trihydrate, quantity: 114.82 mg/ml (equivalent: amoxicillin, qty 100 mg/ml) - oral liquid, powder for - excipient ingredients: silicon dioxide; sodium citrate; purified talc; aspartame; sodium benzoate; citric acid; guar gum; flavour - treatment of the following infections due to susceptible strains of sensitive organisms: note: therapy should be guided by bacteriological studies, including sensitivity tests, and by clinical response. amoxycillin alone or in combination with another antibiotic, may be used in an emergency where the causative organism has not been identified. respiratory tract infections (acute and chronic) including acute otitis media (aom): h. influenzae; streptococcus; s. pneumoniae; staphylococcus, nonpenicillinase producing; e. coli (see microbiology). urogenital infections (complicated and uncomplicated, acute and chronic): e. coli (see microbiology), p. mirabilis and strep. faecalis. gonorrhoea: n. gonorrhoeae (nonpenicillinase producing). skin and skin structure infections: staphlococcus, nonpenicillinase producing; streptococcus, e. coli (see microbiology). prophlaxis of endocarditis: amoxycillin may be used for the prophylaxis of bacterial endocarditis in individuals at particular risk, such as those with a prosthetic heart valve or those who have previously had endocarditis. infections caused by pathogens with established penicillin g susceptibility should preferentially be treated with penicillin g.

VENTOLIN SYRUP salbutamol 2mg/5mL (as sulfate) sugar free oral liquid bottle Australia - English - Department of Health (Therapeutic Goods Administration)

ventolin syrup salbutamol 2mg/5ml (as sulfate) sugar free oral liquid bottle

glaxosmithkline australia pty ltd - salbutamol sulfate, quantity: 0.48 mg/ml (equivalent: salbutamol, qty 0.4 mg/ml) - oral liquid - excipient ingredients: sodium benzoate; hypromellose; citric acid monohydrate; sodium chloride; purified water; sodium citrate dihydrate; saccharin sodium; flavour - indications as at 14 february 2005: ventolin is indicated for the prevention and relief of bronchospasm in bronchial asthma of all types and for the alleviation of any reversible airways obstruction associated with conditions such as chronic bronchitis or emphysema.

VIMPAT lacosamide 10 mg/mL oral solution bottle Australia - English - Department of Health (Therapeutic Goods Administration)

vimpat lacosamide 10 mg/ml oral solution bottle

ucb australia pty ltd t/a ucb pharma division of ucb australia - lacosamide, quantity: 10 mg - solution - excipient ingredients: glycerol; sodium chloride; carmellose sodium; sorbitol solution (70 per cent) (crystallising); macrogol 4000; citric acid; acesulfame potassium; sodium methyl hydroxybenzoate; purified water; flavour - vimpat (lacosamide) tablets and oral solution are indicated as:,? monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in patients with epilepsy aged 16 years and older.,? add-on therapy in the treatment of partial-onset seizures with or without secondary generalisation in patients with epilepsy aged 4 years and older.,? add-on therapy in the treatment of primary generalised tonic-clonic seizures in patients with idiopathic generalised epilepsy aged 4 years and older.

Solu-Medrol 1g powder for injection vial with diluent vial Australia - English - Department of Health (Therapeutic Goods Administration)

solu-medrol 1g powder for injection vial with diluent vial

pfizer australia pty ltd - methylprednisolone sodium succinate, quantity: 1.326 g (equivalent: methylprednisolone, qty 1 g) - injection, powder for - excipient ingredients: monobasic sodium phosphate monohydrate; dibasic sodium phosphate; sodium hydroxide - when oral therapy is not feasible and the strength, dosage form and route of administration of the drug reasonably lend the preparation to the treatment of the condition, solu-medrol powder for injection is indicated only for intravenous or intramuscular use in the following conditions:,endocrine disorders,? primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogues may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance).,? acute adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; mineralocorticoid supplementation may be necessary, particularly when synthetic analogues are used).,? preoperatively and in the event of serious trauma or illness, in patients with known adrenal insufficiency or when adrenocortical reserve is doubtful.,? shock unresponsive to conventional therapy if adrenocortical insufficiency exists or is suspected.,? c

Teicoplanin 200 mg Powder and Solvent for Solution for injection/infusion or oral solution Ireland - English - HPRA (Health Products Regulatory Authority)

teicoplanin 200 mg powder and solvent for solution for injection/infusion or oral solution

noridem enterprises limited - teicoplanin - powder and solvent for solution for injection/infusion - 200 milligram(s) - glycopeptide antibacterials; teicoplanin - glycopeptide antibacterials - it is indicated in adults and in children from birth for the parenteral treatment of the following infections :  complicated skin and soft tissue infections,  bone and joint infections,  hospital acquired pneumonia,  community acquired pneumonia,  complicated urinary tract infections,  infective endocarditis,  peritonitis associated with continuous ambulatory peritoneal dialysis (capd)  bacteraemia that occurs in association with any of the indications listed above.

Teicoplanin 200mg Powder and Solvent for solution for injection/infusion or oral solution Ireland - English - HPRA (Health Products Regulatory Authority)

teicoplanin 200mg powder and solvent for solution for injection/infusion or oral solution

rowex ltd - teicoplanin - powder and solvent for solution for injection/infusion - 200 milligram(s) - glycopeptide antibacterials; teicoplanin - : glycopeptide antibacterials - complicated skin and soft tissue infections, bone and joint infections, hospital acquired pneumonia, community acquired pneumonia, complicated urinary tract infections, infective endocarditis, peritonitis associated with continuous ambulatory peritoneal dialysis (capd), bacteraemia that occurs in association with any of the indications listed above

Teicoplanin 400mg Powder and Solvent for solution for injection/infusion or oral solution Ireland - English - HPRA (Health Products Regulatory Authority)

teicoplanin 400mg powder and solvent for solution for injection/infusion or oral solution

rowex ltd - teicoplanin - powder and solvent for solution for injection/infusion - 400 milligram(s) - glycopeptide antibacterials; teicoplanin - glycopeptide antibacterials - complicated skin and soft tissue infections, bone and joint infections, hospital acquired pneumonia, community acquired pneumonia, • complicated urinary tract infections, infective endocarditis, peritonitis associated with continuous ambulatory peritoneal dialysis (capd)