Australia - English - Department of Health (Therapeutic Goods Administration)

metagenics (aust) pty ltd - calcium amino acid chelate,calcium folinate,chromic chloride hexahydrate,cyanocobalamin,magnesium amino acid chelate,pyridoxal 5-phosphate,riboflavin sodium phosphate,selenomethionine,taurine -

Australia - English - Department of Health (Therapeutic Goods Administration)

key-sun laboratories pty ltd - biotin,calcium citrate tetrahydrate,chromic chloride hexahydrate,colecalciferol,calcium folinate,calcium orotate,calcium pantothenate,choline bitartrate,cyanocobalamin,dunaliella salina,equisetum arvense,folic acid,inositol,magnesium amino acid chelate,magnesium orotate dihydrate,manganese amino acid chelate,nicotinamide,pyridoxal 5-phosphate monohydrate,pyridoxine hydrochloride,phytomenadione,potassium citrate,potassium iodide,riboflavin sodium phosphate,selenomethionine,taurine,thiamine -

Australia - English - Department of Health (Therapeutic Goods Administration)

key-sun laboratories pty ltd - biotin,calcium citrate tetrahydrate,calcium folinate,calcium orotate,calcium pantothenate,choline bitartrate,chromic chloride hexahydrate,colecalciferol,cyanocobalamin,dunaliella salina,equisetum arvense,folic acid,inositol,magnesium amino acid chelate,magnesium orotate dihydrate,manganese amino acid chelate,nicotinamide,phytomenadione,potassium citrate,potassium iodide,pyridoxal 5-phosphate monohydrate,pyridoxine hydrochloride,riboflavin sodium phosphate,selenomethionine,taurine,thiamine -

Australia - English - Department of Health (Therapeutic Goods Administration)

pfizer australia pty ltd - calcium folinate, quantity: 10.8 mg/ml (equivalent: folinic acid, qty 10 mg/ml) - injection, solution - excipient ingredients: hydrochloric acid; sodium hydroxide; sodium chloride; water for injections - leucovorin calcium injection usp is indicated following high dose methotrexate therapy to reduce toxicity (leucovorin rescue). it is also indicated after inadvertent overdosage with methotrexate and in impaired methotrexate elimination.

Australia - English - Department of Health (Therapeutic Goods Administration)

pfizer australia pty ltd - calcium folinate, quantity: 10.8 mg/ml (equivalent: folinic acid, qty 10 mg/ml) - injection, solution - excipient ingredients: water for injections; sodium hydroxide; sodium chloride; hydrochloric acid - leucovorin calcium injection usp is indicated following high dose methotrexate therapy to reduce toxicity (leucovorin rescue). it is also indicated after inadvertent overdosage with methotrexate and in impaired methotrexate elimination.

Australia - English - Department of Health (Therapeutic Goods Administration)

metagenics (aust) pty ltd - chromic chloride hexahydrate, quantity: 66.62 microgram/g (equivalent: chromium, qty 12.99 microgram/g); magnesium amino acid chelate, quantity: 389.6 mg/g (equivalent: magnesium, qty 38.96 mg/g); riboflavin sodium phosphate, quantity: 324.68 microgram/g; calcium folinate, quantity: 21.04 microgram/g (equivalent: folinic acid, qty 19.48 microgram/g); taurine, quantity: 389.6 mg/g; calcium amino acid chelate, quantity: 38.96 mg/g (equivalent: calcium, qty 7.79 mg/g); selenomethionine, quantity: 16.23 microgr - powder, oral - excipient ingredients: colloidal anhydrous silica; steviol glycosides; citric acid; flavour; potable water; polacrilin - maintain/support general health and wellbeing ; maintain/support blood health ; maintain/support cardiovascular system health ; maintain/support heart health ; helps decrease/reduce homocysteine levels ; support healthy stress response in the body

Australia - English - Department of Health (Therapeutic Goods Administration)

pfizer australia pty ltd - calcium folinate, quantity: 10.8 mg/ml (equivalent: folinic acid, qty 10 mg/ml) - injection, solution - excipient ingredients: sodium chloride; water for injections - leucovorin calcium injection usp is indicated following high dose methotrexate therapy to reduce toxicity (leucovorin rescue). it is also indicated after inadvertent overdosage with methotrexate and in impaired methotrexate elimination.

New Zealand - English - Medsafe (Medicines Safety Authority)

novartis new zealand ltd - calcium folinate pentahydrate 12.71 mg/ml equivalent to 10 mg/ml folinic acid - concentrate for injection - 10 mg/ml - active: calcium folinate pentahydrate 12.71 mg/ml equivalent to 10 mg/ml folinic acid excipient: hydrochloric acid nitrogen sodium chloride sodium hydroxide water for injection - · as rescue therapy to reduce toxicity following high-dose methotrexate therapy. · has shown good results in the treatment of certain megaloblastic anaemias resulting from folic acid deficiency. this mainly occurs in infants, during pregnancy, in malabsorption syndromes, liver diseases, sprue and malnutrition. it is not more effective than folic acid for these conditions · overdosage of methotrexate and in impaired methotrexate elimination · reducing the toxicity and circumventing the effect of folic acid antagonists

Australia - English - Department of Health (Therapeutic Goods Administration)

interclinical laboratories pty ltd - calcium amino acid chelate,calcium carbonate,ergocalciferol -

Australia - English - Department of Health (Therapeutic Goods Administration)

pfizer australia pty ltd - calcium folinate, quantity: 324.1 mg (equivalent: folinic acid, qty 300 mg) - injection - excipient ingredients: sodium hydroxide; hydrochloric acid; water for injections; sodium chloride - leucovorin calcium has shown good results in the treatment of certain megaloblastic anaemias resulting from folic acid deficiency.this mainly occurs in infants, during pregnancy, in malabsorption syndromes, liver disease, sprue and malnutrition. it is not more effective than folic acid for these conditions. leucovorin calcium has also shown good results in reducing the toxicity and circumventing the effect of folic acid antagonists, if therapeutically desired.