TOPOTECAN KABI Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

topotecan kabi

fresenius kabi australia pty ltd - topotecan hydrochloride, quantity: 4.346 mg - injection, powder for - excipient ingredients: mannitol; tartaric acid; hydrochloric acid; sodium hydroxide - topotecan is indicated as single agent therapy for the treatment of patients with: - small cell lung carcinoma, after failure of first line chemotherapy. - metastatic carcinoma of the ovary after failure of first-line or subsequent therapy.

ADDAVEN concentrated injection ampoule Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

addaven concentrated injection ampoule

fresenius kabi australia pty ltd - chromic chloride hexahydrate, quantity: 5.33 microgram/ml; ferric chloride hexahydrate, quantity: 540 microgram/ml; sodium selenite, quantity: 17.29 microgram/ml; sodium fluoride, quantity: 210 microgram/ml; cupric chloride dihydrate, quantity: 102.3 microgram/ml; potassium iodide, quantity: 16.6 microgram/ml; sodium molybdate dihydrate, quantity: 4.85 microgram/ml; manganese chloride tetrahydrate, quantity: 19.79 microgram/ml; zinc chloride, quantity: 1.05 mg/ml - injection, concentrated - excipient ingredients: water for injections; hydrochloric acid; xylitol - to meet basal to moderately increased requirements of trace elements in parenteral nutrition in adults, when either oral or enteral nutrition is inappropriate

VITALIPID N INFANT 10mL injection emulsion ampoule Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

vitalipid n infant 10ml injection emulsion ampoule

fresenius kabi australia pty ltd - dl-alpha-tocopherol, quantity: 0.64 mg/ml; retinol palmitate, quantity: 135.3 microgram/ml; phytomenadione, quantity: 20 microgram/ml; ergocalciferol, quantity: 1 microgram/ml - injection, concentrated - excipient ingredients: sodium hydroxide; water for injections; glycerol; egg lecithin; soya oil - vitalipid n infant is indicated as a supplement in complete intravenous nutrition to meet the daily requirements of the fat- soluble vitamins a, d2, e and k1 in paediatric patients up to 11 years of age.

VITALIPID N ADULT 10mL injection ampoule Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

vitalipid n adult 10ml injection ampoule

fresenius kabi australia pty ltd - phytomenadione, quantity: 15 microgram/ml; ergocalciferol, quantity: 0.5 microgram/ml; retinol palmitate, quantity: 194.1 microgram/ml; dl-alpha-tocopherol, quantity: 0.91 mg/ml - injection, concentrated - excipient ingredients: soya oil; egg lecithin; glycerol; water for injections; sodium hydroxide - vitalipid n adult is indicated as a supplement in complete intravenous nutrition to meet the daily requirements of the fat- soluble vitamins a, d2, e and k1.

KETOROLAC KABI ketorolac trometamol 30 mg/1 mL solution for injection, vial Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

ketorolac kabi ketorolac trometamol 30 mg/1 ml solution for injection, vial

fresenius kabi australia pty ltd - ketorolac trometamol, quantity: 30 mg/ml - injection, solution - excipient ingredients: ethanol; sodium chloride; water for injections; hydrochloric acid; sodium hydroxide - ketorolac kabi is indicated for the short-term management of moderately severe, acute pain following surgical procedures. the total duration of ketorolac use should not exceed five days.,it is recommended that ketorolac parenteral be used in the immediate post-operative period. patients can then be converted to the oral formulation (dependent on their analgesic needs), as outlined in the "dose and method of administration" section (refer to "conversion from parenteral to oral therapy"). the total period of treatment utilising the oral and/or intramuscular route of administration is not to exceed five days.,general,ketorolac is not recommended for use as an obstetrical pre-operative medication or for obstetrical analgesia because it has not been adequately studied for use in these circumstances and because the known effects of drugs that inhibit prostaglandin biosynthesis on uterine contraction and foetal circulation.,there is no satisfactory evidence for the use of ketorolac in acute exacerbations of chronic painful inflammatory conditions (e.g. rheumatoid or osteoarthritis).

FLUMAZENIL KABI flumazenil 1mg/10mL solution for injection ampoules Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

flumazenil kabi flumazenil 1mg/10ml solution for injection ampoules

fresenius kabi australia pty ltd - flumazenil, quantity: 0.1 mg/ml - injection, solution - excipient ingredients: acetic acid; sodium hydroxide; disodium edetate; sodium chloride; water for injections - flumazenil kabi is indicated for use in hospitalised patients for the reversal of acute benzodiazepine effects (overdose or therapeutic). hospitalised patients are patients admitted to hospital, inpatient care and under continued professional observation while under the influence of flumazenil. not to be used in outpatients or short stay patients. not to be used as a diagnostic.

FLUMAZENIL KABI flumazenil 0.5mg/5mL solution for injection ampoules Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

flumazenil kabi flumazenil 0.5mg/5ml solution for injection ampoules

fresenius kabi australia pty ltd - flumazenil, quantity: 0.1 mg/ml - injection, solution - excipient ingredients: water for injections; acetic acid; sodium chloride; sodium hydroxide; disodium edetate - flumazenil kabi is indicated for use in hospitalised patients for the reversal of acute benzodiazepine effects (overdose or therapeutic). hospitalised patients are patients admitted to hospital, inpatient care and under continued professional observation while under the influence of flumazenil. not to be used in outpatients or short stay patients. not to be used as a diagnostic.

WATER FOR INJECTIONS BP, water for injections, 5 mL, solution for injection, ampoule Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

water for injections bp, water for injections, 5 ml, solution for injection, ampoule

fresenius kabi australia pty ltd - water for injections, quantity: 5 ml - injection, solution - excipient ingredients: - water for injections bp is used to dissolve or dilute substances or preparations for parenteral administration. ,water for injections bp may also be used as an irrigating solution for small wounds or during minor surgical procedures.

WATER FOR INJECTIONS BP, water for injections, 20 mL, solution for injection, ampoule Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

water for injections bp, water for injections, 20 ml, solution for injection, ampoule

fresenius kabi australia pty ltd - water for injections, quantity: 20 ml - injection, solution - excipient ingredients: - water for injections bp is used to dissolve or dilute substances or preparations for parenteral administration. ,water for injections bp may also be used as an irrigating solution for small wounds or during minor surgical procedures.

WATER FOR INJECTIONS BP, water for injections, 10 mL, solution for injection, ampoule Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

water for injections bp, water for injections, 10 ml, solution for injection, ampoule

fresenius kabi australia pty ltd - water for injections, quantity: 10 ml - injection, solution - excipient ingredients: - water for injections bp is used to dissolve or dilute substances or preparations for parenteral administration. ,water for injections bp may also be used as an irrigating solution for small wounds or during minor surgical procedures.