אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - sumatriptan succinate, quantity: 70 mg (equivalent: sumatriptan, qty 50 mg) - tablet, film coated - excipient ingredients: microcrystalline cellulose; magnesium stearate; lactose monohydrate; croscarmellose sodium; titanium dioxide; hypromellose; macrogol 8000; triacetin; iron oxide yellow; iron oxide red; polydextrose - iptam tablets are indicated for the acute relief of migraine attacks with or without aura. there is no information available on the use of iptam in the treatment of basilar or hemiplegic migraines.

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - piroxicam, quantity: 20 mg - tablet, dispersible - excipient ingredients: hyprolose; sodium stearylfumarate; lactose monohydrate; microcrystalline cellulose - symptomatic treatment of rheumatoid arthritis, osteoarthritis and ankylosing spondylitis.

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - piroxicam, quantity: 10 mg - tablet, dispersible - excipient ingredients: sodium stearylfumarate; hyprolose; microcrystalline cellulose; lactose monohydrate - symptomatic treatment of rheumatoid arthritis, osteoarthritis and ankylosing spondylitis.

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - pravastatin sodium, quantity: 40 mg - tablet, uncoated - excipient ingredients: microcrystalline cellulose; croscarmellose sodium; lactose monohydrate; purified talc; magnesium stearate; aluminium magnesium silicate; povidone - 1. as an adjunct to diet for treatment of hyper cholesterolemia. prior to initiating therapy with pravastatin, secondary causes of hypercholesterolemia (e.g., poorly controlled diabetes mellitus, hypothyroidism, nephrotic syndrome, dysproteinemias, obstructive liver disease, other drug therapy, alcoholism) should be identified and treated. 2. pravastatin is indicated in patients with previous myocardial infarction including those who have normal (4.0 to 5.5 mmol/l) serum cholesterol levels. 3. pravastatin is indicated in patients with unstable angina pectoris (see clinical trials). 4. cholstat is indicated as an adjunct to diet and lifestyle modification for the treatment of heterozygous familial hypercholesterolaemia in children and adolescent patients aged 8 years and older (see clinical trials).

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - pravastatin sodium, quantity: 20 mg - tablet, uncoated - excipient ingredients: povidone; magnesium stearate; microcrystalline cellulose; croscarmellose sodium; lactose monohydrate; aluminium magnesium silicate; purified talc - 1. as an adjunct to diet for treatment of hyper cholesterolemia. prior to initiating therapy with pravastatin, secondary causes of hypercholesterolemia (e.g., poorly controlled diabetes mellitus, hypothyroidism, nephrotic syndrome, dysproteinemias, obstructive liver disease, other drug therapy, alcoholism) should be identified and treated. 2. pravastatin is indicated in patients with previous myocardial infarction including those who have normal (4.0 to 5.5 mmol/l) serum cholesterol levels. 3. pravastatin is indicated in patients with unstable angina pectoris (see clinical trials). 4. cholstat is indicated as an adjunct to diet and lifestyle modification for the treatment of heterozygous familial hypercholesterolaemia in children and adolescent patients aged 8 years and older (see clinical trials).

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - pravastatin sodium, quantity: 10 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; croscarmellose sodium; povidone; purified talc; aluminium magnesium silicate; magnesium stearate; microcrystalline cellulose - 1. as an adjunct to diet for treatment of hyper cholesterolemia. prior to initiating therapy with pravastatin, secondary causes of hypercholesterolemia (e.g., poorly controlled diabetes mellitus, hypothyroidism, nephrotic syndrome, dysproteinemias, obstructive liver disease, other drug therapy, alcoholism) should be identified and treated. 2. pravastatin is indicated in patients with previous myocardial infarction including those who have normal (4.0 to 5.5 mmol/l) serum cholesterol levels. 3. pravastatin is indicated in patients with unstable angina pectoris (see clinical trials). 4. cholstat is indicated as an adjunct to diet and lifestyle modification for the treatment of heterozygous familial hypercholesterolaemia in children and adolescent patients aged 8 years and older (see clinical trials).

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - indapamide hemihydrate, quantity: 2.5 mg - tablet - excipient ingredients: lactose; microcrystalline cellulose; sodium starch glycollate; croscarmellose sodium; magnesium stearate; titanium dioxide; hypromellose; quinoline yellow; brilliant scarlet 4r; cochineal; macrogol 400 - treatment of hypertension. it may be tried as a sole therapeutic agent in the treatment of hypertension. normally indapamide is used as the initail agent in multiple drug regimes.

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - piroxicam, quantity: 20 mg - capsule, hard - excipient ingredients: lactose monohydrate; maize starch; magnesium stearate; sodium starch glycollate; sodium lauryl sulfate; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; purified water; shellac; strong ammonia solution; iron oxide black; potassium hydroxide; titanium dioxide; gelatin - symptomatic treatment of rheumatoid arthritis, osteoarthritis and ankylosing spondylitis.

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - piroxicam, quantity: 10 mg - capsule, hard - excipient ingredients: lactose monohydrate; maize starch; magnesium stearate; sodium starch glycollate; sodium lauryl sulfate; propylene glycol; ethanol; butan-1-ol; purified water; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide; titanium dioxide; iron oxide yellow; iron oxide red; gelatin - symptomatic treatment of rheumatoid arthritis, osteoarthritis and ankylosing spondylitis.

אוסטרליה - אנגלית - Department of Health (Therapeutic Goods Administration)

alphapharm pty ltd - naproxen, quantity: 500 mg - tablet - excipient ingredients: microcrystalline cellulose; magnesium stearate; lactose monohydrate; sodium starch glycollate; pregelatinised maize starch; maize starch; purified talc; colloidal anhydrous silica - treatment of rheumatoid arthritis, juvenile rheumatoid arthritis and osteoarthritis, ankylosing spondylitis; symptomatic treatment of primary dysmenorrhoea, relief of acute and/or chronic pain states in which there is an inflammatory component, and as an analgesic in acute migraine attack.