ASPEN CODEINE codeine phosphate hemihydrate 30mg tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

aspen codeine codeine phosphate hemihydrate 30mg tablet blister pack

aspen pharmacare australia pty ltd - codeine phosphate hemihydrate, quantity: 30 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; maize starch; magnesium stearate - aspen codeine tablets are indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

ASPEN METHADONE SYRUP 25mg/5mL oral liquid Australia - English - Department of Health (Therapeutic Goods Administration)

aspen methadone syrup 25mg/5ml oral liquid

aspen pharma pty ltd - methadone hydrochloride, quantity: 5 mg/ml - oral liquid, solution - excipient ingredients: glycerol; sodium benzoate; purified water; sorbitol solution (70 per cent) (non-crystallising); ethanol; sunset yellow fcf; flavour - methadone syrup is indicated for the treatment of dependence on opioid drugs.,methadone syrup is indicated for the management of severe pain where: (i) other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and (ii) the pain is opioid-responsive, and (iii) requires daily, continuous, long-term treatment.,methadone syrup is not indicated for use in chronic non-cancer pain other than in exceptional circumstances.,methadone syrup is not indicated as an as-needed (prn) analgesia.,methadone syrup is not recommended for use in ambulant patients.

ASPEN DEXAMFETAMINE dexamphetamine sulphate 5mg tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

aspen dexamfetamine dexamphetamine sulphate 5mg tablet bottle

aspen pharmacare australia pty ltd - dexamfetamine sulfate, quantity: 5 mg - tablet, uncoated - excipient ingredients: povidone; wheat starch; magnesium stearate; lactose monohydrate - indications as at 22 january 1997: narcolepsy and hyperkinetic behaviour disorders in children.

ASPEN CIPROFLOXACIN ciprofloxacin injection for intravenous infusion 200mg/100mL bag Australia - English - Department of Health (Therapeutic Goods Administration)

aspen ciprofloxacin ciprofloxacin injection for intravenous infusion 200mg/100ml bag

aspen pharmacare australia pty ltd - ciprofloxacin, quantity: 2 mg/ml - injection, intravenous infusion - excipient ingredients: lactic acid; glucose monohydrate; water for injections - aspen ciprofloxacin injection for intravenous infusion is indicated for use in the following. hospitalised adult patients in whom oral ciprofloxacin is indicated but cannot be administered or where the oral form is inappropriate. for the treatment of serious or life-threatening infections due to sensitive organisms involving the following organ systems. lower respiratory tract infections (gram-negative organisms), skin and skin structure, septicaemia, bone and joint, urinary tract. inhalational anthrax (post exposure): to reduce the incidence or progression of disease following exposure to aerosolized bacillus anthracis. ciprofloxacin serum concentrations achieved in humans serve as a surrogate endpoint reasonably likely to predict clinical benefit and provide the basis for this indication. note. because gram-positive organisms are generally less sensitive to ciprofloxacin, it may not be the drug of choice in cases with gram-positive infections, such as pneumonia due to streptococcus pneumoniae. if anaerobic

ASPEN CIPROFLOXACIN ciprofloxacin injection for intravenous infusion 100mg/50mL bag Australia - English - Department of Health (Therapeutic Goods Administration)

aspen ciprofloxacin ciprofloxacin injection for intravenous infusion 100mg/50ml bag

aspen pharmacare australia pty ltd - ciprofloxacin, quantity: 2 mg/ml - injection, intravenous infusion - excipient ingredients: lactic acid; glucose monohydrate; water for injections - aspen ciprofloxacin injection for intravenous infusion is indicated for use in the following. hospitalised adult patients in whom oral ciprofloxacin is indicated but cannot be administered or where the oral form is inappropriate. for the treatment of serious or life-threatening infections due to sensitive organisms involving the following organ systems. lower respiratory tract infections (gram-negative organisms), skin and skin structure, septicaemia, bone and joint, urinary tract. inhalational anthrax (post exposure): to reduce the incidence or progression of disease following exposure to aerosolized bacillus anthracis. ciprofloxacin serum concentrations achieved in humans serve as a surrogate endpoint reasonably likely to predict clinical benefit and provide the basis for this indication. note. because gram-positive organisms are generally less sensitive to ciprofloxacin, it may not be the drug of choice in cases with gram-positive infections, such as pneumonia due to streptococcus pneumoniae. if anaerobic