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

eli lilly australia pty ltd - atomoxetine hydrochloride, quantity: 68.56 mg (equivalent: atomoxetine, qty 60 mg) - capsule, hard - excipient ingredients: pregelatinised maize starch; gelatin; indigo carmine; titanium dioxide; dimeticone 350; iron oxide yellow; sodium lauryl sulfate; propylene glycol; ethanol; butan-1-ol; purified water; isopropyl alcohol; shellac; iron oxide black; simethicone; strong ammonia solution; potassium hydroxide - strattera is indicated for the treatment of attention deficit hyperactivity disorder (adhd) as defined by dsm-iv criteria in children 6 years of age and older, adolescents and adults.

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

eli lilly australia pty ltd - atomoxetine hydrochloride, quantity: 45.71 mg (equivalent: atomoxetine, qty 40 mg) - capsule, hard - excipient ingredients: sodium lauryl sulfate; indigo carmine; titanium dioxide; gelatin; pregelatinised maize starch; dimeticone 350; propylene glycol; ethanol; butan-1-ol; purified water; isopropyl alcohol; shellac; iron oxide black; simethicone; strong ammonia solution; potassium hydroxide - strattera is indicated for the treatment of attention deficit hyperactivity disorder (adhd) as defined by dsm-iv criteria in children 6 years of age and older, adolescents and adults.

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

eli lilly australia pty ltd - atomoxetine hydrochloride, quantity: 28.57 mg (equivalent: atomoxetine, qty 25 mg) - capsule, hard - excipient ingredients: titanium dioxide; pregelatinised maize starch; dimeticone 350; gelatin; indigo carmine; sodium lauryl sulfate; propylene glycol; ethanol; butan-1-ol; purified water; isopropyl alcohol; shellac; iron oxide black; simethicone; strong ammonia solution; potassium hydroxide - strattera is indicated for the treatment of attention deficit hyperactivity disorder (adhd) as defined by dsm-iv criteria in children 6 years of age and older, adolescents and adults.

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

eli lilly australia pty ltd - atomoxetine hydrochloride, quantity: 20.57 mg (equivalent: atomoxetine, qty 18 mg) - capsule, hard - excipient ingredients: pregelatinised maize starch; sodium lauryl sulfate; dimeticone 350; titanium dioxide; iron oxide yellow; gelatin; propylene glycol; ethanol; butan-1-ol; purified water; isopropyl alcohol; shellac; iron oxide black; simethicone; strong ammonia solution; potassium hydroxide - strattera is indicated for the treatment of attention deficit hyperactivity disorder (adhd) as defined by dsm-iv criteria in children 6 years of age and older, adolescents and adults.

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

eli lilly australia pty ltd - atomoxetine hydrochloride, quantity: 11.43 mg (equivalent: atomoxetine, qty 10 mg) - capsule, hard - excipient ingredients: titanium dioxide; pregelatinised maize starch; gelatin; sodium lauryl sulfate; dimeticone 350; propylene glycol; ethanol; butan-1-ol; purified water; isopropyl alcohol; shellac; iron oxide black; simethicone; strong ammonia solution; potassium hydroxide - strattera is indicated for the treatment of attention deficit hyperactivity disorder (adhd) as defined by dsm-iv criteria in children 6 years of age and older, adolescents and adults.

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

eli lilly australia pty ltd - atomoxetine hydrochloride, quantity: 5.71 mg (equivalent: atomoxetine, qty 5 mg) - capsule, hard - excipient ingredients: dimeticone 350; gelatin; sodium lauryl sulfate; pregelatinised maize starch; iron oxide yellow; propylene glycol; ethanol; butan-1-ol; purified water; isopropyl alcohol; shellac; iron oxide black; simethicone; strong ammonia solution; potassium hydroxide - strattera is indicated for the treatment of attention deficit hyperactivity disorder (adhd) as defined by dsm-iv criteria in children 6 years of age and older, adolescents and adults.

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

alphapharm pty ltd - alprazolam, quantity: 2 mg - tablet, uncoated - excipient ingredients: docusate sodium; sodium starch glycollate; povidone; maize starch; sodium benzoate; lactose monohydrate; magnesium stearate; microcrystalline cellulose; colloidal anhydrous silica - anxiety. short-term symptomatic treatment of anxiety including treatment of anxious patients with some symptoms of depression. panic disorder. the treatment of panic disorder with or without some phobic avoidance, and for blocking or attenuation of panic attacks and phobias in patients who have agoraphobia with panic attacks. the diagnostic criteria for panic disorder in dsm-iii-r are as follows: the panic attacks (discrete periods of intense fear or discomfort), at least initially, are unexpected. later in the course of this disturbance, certain situations (eg. driving a car or being in a crowded place) may become associated with having a panic attack. these panic attacks are not triggered by situations in which the person is the focus of others' attention (as in social phobia). the diagnosis requires four such attacks within a four week period, or one or more attacks followed by at least a month of persistent fear of having another attack. the panic attacks must be characterised by at least four of the following symptoms: dyspnoea or smothering sensations; dizziness, unsteady feelings or faintness; palpitations or tachycardia; trembling or shaking; sweating; choking; nausea or abdominal distress; depersonalisation or derealisation; paraesthesiae; flushes (hot flashes) or chills; chest pain or discomfort; fear of dying; fear of going crazy or of doing something uncontrolled. note: attacks involving four or more symptoms are panic attacks; attacks involving fewer than four are limited symptom attacks. at least some of the panic attack symptoms must develop suddenly and increase in intensity within ten minutes of the beginning of the first symptom noticed in the attack. the panic attack must not be attributable to some known organic factor, eg. amphetamine or caffeine, intoxication, hyper-thyroidism. the efficacy of alprazolam in conditions where the above criteria are not met has not been established. the risk versus benefits of alprazolam use in milder disorders, which do not meet the above criteria, has not been evaluated. although current evidence supports the long-term clinical effectiveness of alprazolam in panic disorder, the continuing use of alprazolam needs to be weighed against the difficulties that can occur with dependence and discontinuation. the results of a long-term study in patients taking alprazolam (ie. beyond three months) suggest that many patients continue to benefit from alprazolam therapy and that alprazolam efficacy is maintained for up to eight months. the physician should periodically reassess the usefulness of the drug for each patient. a comparative study of alprazolam and placebo in the treatment of panic attacks in patients with panic disorder involved 543 patients over an eight week period. alprazolam was significantly more effective than placebo in reducing the total number of panic attacks (p<0.0001); at week 4, 46.8% of alprazolam patients had achieved zero total panic attacks when compared to 27.1% of placebo patients. panic disorders are often severe, chronic illnesses that cause a high level of work and social disability, increased substance abuse and potentially increased morbidity and mortality. psychological and social factors are important in the pathogenesis of panic attacks, either acting alone or in combination with biological factors. prolonged pharmacological therapy may be used as an adjunct to psychosocial therapy in the treatment of patients with panic disorders.

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

pfizer australia pty ltd - rifabutin, quantity: 150 mg - capsule, hard - excipient ingredients: microcrystalline cellulose; sodium lauryl sulfate; magnesium stearate; silicon dioxide; iron oxide red; titanium dioxide; gelatin; propylene glycol; butan-1-ol; isopropyl alcohol; strong ammonia solution; simethicone; ethanol; shellac; sulfuric acid; povidone; tert-butyl alcohol; sodium hydroxide - mycobutin is indicated for: the prophylaxis of m.avium-intracellulare complex (mac) infections in patients with advanced hiv infection (cd4 counts lower than 200/ul); the treatment of infections caused by mac and other atypical mycobacteria, including in immunocompromised patients; the treatment of chronic multi-drug resistant pulmonary tuberculosis in the presence of rifampicin resistant, rifabutin-sensitive m.tuberculosis strains; the treatment of newly diagnosed pulmonary tuberculosis in the presence of rifampicin resistant, rifabutin sensitive m.tuberculosis strains. in accordance with the commonly accepted criteria for the treatment of mycobacterial infections, mycobutin should always be given in combination with other anti-mycobacterial drugs not belonging to the family of rifamycins.

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

alphapharm pty ltd - alprazolam, quantity: 1 mg - tablet, uncoated - excipient ingredients: sodium starch glycollate; maize starch; docusate sodium; colloidal anhydrous silica; magnesium stearate; sodium benzoate; lactose monohydrate; indigo carmine aluminium lake; microcrystalline cellulose; povidone - for short-term symptomatic treatment of anxiety including treatment of anxious patients with some symptoms of depression. alprazolam is not recommended as primary therapy in patients with depression. for the treatment of panic disorder with or without some phobic avoidance, and for blocking or attenuation of panic attacks and phobias in patients who have agoraphobia with panic attacks. indications as at 17 december 2001 : anxiety. short-term symptomatic treatment of anxiety including treatment of anxious patients with some symptoms of depression. panic disorder. the treatment of panic disorder with or without some phobic avoidance, and for blocking or attenuation of panic attacks and phobias in patients who have agoraphobia with panic attacks. the diagnostic criteria for panic disorder in dsm-iii-r are as follows: the panic attacks (discrete periods of intense fear or discomfort), at least initially, are unexpected. later in the course of this disturbance, certain situations (e.g. driving a car or being

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

alphapharm pty ltd - alprazolam, quantity: 0.5 mg - tablet, uncoated - excipient ingredients: microcrystalline cellulose; magnesium stearate; povidone; docusate sodium; colloidal anhydrous silica; indigo carmine aluminium lake; sodium starch glycollate; maize starch; erythrosine aluminium lake; lactose monohydrate; sodium benzoate - for short-term symptomatic treatment of anxiety including treatment of anxious patients with some symptoms of depression. alprazolam is not recommended as primary therapy in patients with depression. for the treatment of panic disorder with or without some phobic avoidance, and for blocking or attenuation of panic attacks and phobias in patients who have agoraphobia with panic attacks. indications as at 17 december 2001 : anxiety. short-term symptomatic treatment of anxiety including treatment of anxious patients with some symptoms of depression. panic disorder. the treatment of panic disorder with or without some phobic avoidance, and for blocking or attenuation of panic attacks and phobias in patients who have agoraphobia with panic attacks. the diagnostic criteria for panic disorder in dsm-iii-r are as follows: the panic attacks (discrete periods of intense fear or discomfort), at least initially, are unexpected. later in the course of this disturbance, certain situations (e.g. driving a car or being