CYPROTERONE SANDOZ cyproterone acetate 100 mg tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

cyproterone sandoz cyproterone acetate 100 mg tablet blister pack

sandoz pty ltd - cyproterone acetate, quantity: 100 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; microcrystalline cellulose; croscarmellose sodium; povidone; magnesium stearate - inoperable prostatic carcinoma. to suppress flare with initial luteinising hormone releasing hormone (lhrh) analogue therapy; in long-term palliative treatment where lhrh analogues or surgery are ineffective, not tolerated, contraindicated or where oral therapy is preferred; in the treatment of hot flushes in patients treated with lhrh analogues or who have had orchidectomy.

CYPROTERONE SANDOZ cyproterone acetate 50 mg tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

cyproterone sandoz cyproterone acetate 50 mg tablet bottle

sandoz pty ltd - cyproterone acetate, quantity: 50 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; microcrystalline cellulose; croscarmellose sodium; povidone; magnesium stearate - women: moderately severe to severe signs of androgenisation. moderately severe/severe forms of hirsutism; moderately severe/severe androgen dependent loss of scalp hair (moderately severe/severe androgenic alopecia); moderately severe/severe forms of acne and/or seborrhoea associated with other features of androgenisation. cyproterone sandoz 50mg inhibits the influence of male sex hormones which are also produced by the female. it is thus possible to treat diseases in women caused by either increased production of androgens or a particular sensitivity to these hormones. hirsutism and alopecia may be expected to recur over a period of time after cessation of treatment. if cyproterone sandoz 50mg is taken during pregnancy, the properties of the preparation may lead to signs of feminisation in the male foetus. therefore, in women of childbearing potential, pregnancy must be excluded at the commencement of treatment and ethinyloestradiol taken as well to ensure contraception. this also promotes regular menstruation. men: reduction to drive in sexual deviations. cyproterone sandoz 50mg reduces the force of the sexual urge in men with sexual deviations. whilst under treatment the man can control himself better in a predisposing stimulatory situation, but there is no influence on any deviating direction of sexual drive. abnormal patterns of sexual behaviour require treatment when they are distressing to the patient. a prerequisite for therapy is the desire by the patient for treatment. cyproterone sandoz 50mg should be supplemented by psychotherapeutic and sociotherapeutic measures in order to exploit the period to reduced drive for personal and social reorientation. inoperable prostatic carcinoma. to suppress flare with initial luteinising hormone releasing hormone (lhrh) analogue therapy; in long-term palliative treatment where lhrh analogues or surgery are ineffective, not tolerated, contraindicated or where oral therapy is preferred; in the treatment of hot flushes in patients treated with lhrh analogues or who have had orchidectomy.

REMSIMA infliximab 120 mg solution for injection prefilled syringe in auto-injector pen Australia - English - Department of Health (Therapeutic Goods Administration)

remsima infliximab 120 mg solution for injection prefilled syringe in auto-injector pen

celltrion healthcare australia pty ltd - infliximab, quantity: 120 mg - injection, solution - excipient ingredients: acetic acid; sodium acetate trihydrate; sorbitol; polysorbate 80; water for injections - rheumatoid arthritis in adults remsima in combination with methotrexate, is indicated for the reduction of signs and symptoms and prevention of structural joint damage (erosions and joint space narrowing) in: - patients with active disease despite treatment with methotrexate - patients with active disease who have not previously received methotrexate.,remsima should be given in combination with methotrexate. efficacy and safety in rheumatoid arthritis have been demonstrated only in combination with methotrexate.,ankylosing spondylitis remsima is indicated for the reduction of signs and symptoms and improvement in physical function in patients with active disease.,psoriatic arthritis remsima is indicated for the treatment of the signs and symptoms, as well as for the improvement in physical function in adult patients with active and progressive psoriatic arthritis who have responded inadequately to disease-modifying anti-rheumatic drug (dmard) therapy. remsima may be administered in combination with methotrexate.,psoriasis remsima is indicated for the treatment of adult patients with moderate to severe plaque psoriasis for whom phototherapy or conventional systemic treatments have been inadequate or are inappropriate. safety and efficacy beyond 12 months have not been established.,crohn?s disease in adults remsima is indicated for the treatment of moderate to severe crohn?s disease, to reduce the signs and symptoms and to induce and maintain clinical remission in patients who have an inadequate response to conventional therapies.,refractory fistulising crohn?s disease remsima is indicated for reducing the number of draining enterocutaneous and rectovaginal fistulas and maintaining fistula closure in adult patients.,ulcerative colitis in adults remsimais indicated for the treatment of moderately severe to severe active ulcerative colitis in patients who have had an inadequate response to conventional therapy.

REMSIMA infliximab 120 mg solution for injection prefilled syringe with safety guard Australia - English - Department of Health (Therapeutic Goods Administration)

remsima infliximab 120 mg solution for injection prefilled syringe with safety guard

celltrion healthcare australia pty ltd - infliximab, quantity: 120 mg - injection, solution - excipient ingredients: acetic acid; sodium acetate trihydrate; sorbitol; polysorbate 80; water for injections - rheumatoid arthritis in adults remsima in combination with methotrexate, is indicated for the reduction of signs and symptoms and prevention of structural joint damage (erosions and joint space narrowing) in: - patients with active disease despite treatment with methotrexate - patients with active disease who have not previously received methotrexate.,remsima should be given in combination with methotrexate. efficacy and safety in rheumatoid arthritis have been demonstrated only in combination with methotrexate.,ankylosing spondylitis remsima is indicated for the reduction of signs and symptoms and improvement in physical function in patients with active disease.,psoriatic arthritis remsima is indicated for the treatment of the signs and symptoms, as well as for the improvement in physical function in adult patients with active and progressive psoriatic arthritis who have responded inadequately to disease-modifying anti-rheumatic drug (dmard) therapy. remsima may be administered in combination with methotrexate.,psoriasis remsima is indicated for the treatment of adult patients with moderate to severe plaque psoriasis for whom phototherapy or conventional systemic treatments have been inadequate or are inappropriate. safety and efficacy beyond 12 months have not been established.,crohn?s disease in adults remsima is indicated for the treatment of moderate to severe crohn?s disease, to reduce the signs and symptoms and to induce and maintain clinical remission in patients who have an inadequate response to conventional therapies.,refractory fistulising crohn?s disease remsima is indicated for reducing the number of draining enterocutaneous and rectovaginal fistulas and maintaining fistula closure in adult patients.,ulcerative colitis in adults remsimais indicated for the treatment of moderately severe to severe active ulcerative colitis in patients who have had an inadequate response to conventional therapy.

REMSIMA infliximab 120 mg solution for injection prefilled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

remsima infliximab 120 mg solution for injection prefilled syringe

celltrion healthcare australia pty ltd - infliximab, quantity: 120 mg - injection, solution - excipient ingredients: acetic acid; sodium acetate trihydrate; sorbitol; polysorbate 80; water for injections - rheumatoid arthritis in adults remsima in combination with methotrexate, is indicated for the reduction of signs and symptoms and prevention of structural joint damage (erosions and joint space narrowing) in: - patients with active disease despite treatment with methotrexate - patients with active disease who have not previously received methotrexate.,remsima should be given in combination with methotrexate. efficacy and safety in rheumatoid arthritis have been demonstrated only in combination with methotrexate.,ankylosing spondylitis remsima is indicated for the reduction of signs and symptoms and improvement in physical function in patients with active disease.,psoriatic arthritis remsima is indicated for the treatment of the signs and symptoms, as well as for the improvement in physical function in adult patients with active and progressive psoriatic arthritis who have responded inadequately to disease-modifying anti-rheumatic drug (dmard) therapy. remsima may be administered in combination with methotrexate.,psoriasis remsima is indicated for the treatment of adult patients with moderate to severe plaque psoriasis for whom phototherapy or conventional systemic treatments have been inadequate or are inappropriate. safety and efficacy beyond 12 months have not been established.,crohn?s disease in adults remsima is indicated for the treatment of moderate to severe crohn?s disease, to reduce the signs and symptoms and to induce and maintain clinical remission in patients who have an inadequate response to conventional therapies.,refractory fistulising crohn?s disease remsima is indicated for reducing the number of draining enterocutaneous and rectovaginal fistulas and maintaining fistula closure in adult patients.,ulcerative colitis in adults remsimais indicated for the treatment of moderately severe to severe active ulcerative colitis in patients who have had an inadequate response to conventional therapy.

SCHERING GA GROWTH REGULANT Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

schering ga growth regulant

schering pty ltd - gibberellic acid - plant regulator - grape - currant (dried fruit) | grape - sultana | grape - sultana (dried fruit) | malting barley | mandarin | navel orange | ora - advance or delay maturity (inc. rind) | bunch elongation (stretch) | crop management | fruit thinning | increase fruit size or hasten maturity | increase fruit storage quality | increase storage life | promoted or delayed fruit maturity | reduce germination period | delay ageing | delay harvest | delay maturity | fruit thinning | longer storage life

SCHERING MONITOR 580 INSECTICIDE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

schering monitor 580 insecticide

schering pty ltd - methamidophos - insecticide - cabbage | capsicum or pepper | cauliflower | gladiolus | peach - see label for variety | peanut | potato | tomato | evening-flow - aphid | cabbage center grub | cabbage moth | cabbage white butterfly | cluster caterpillar | common brown leafhopper | green peach aphid | helicoverpa spp. | potato moth | potato moth or tobacco leafminer | thrip | tomato grub | white fringed weevil | corn earworm | cotton bollworm | diamondback moth | heliothis | jassid | native budworm | naupactus leucoloma | potato tuber moth | thrips spp. | tobacco budworm | tobacco leafminer | tomato grub

SCHERING ORTHENE 750 SP INSECTICIDE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

schering orthene 750 sp insecticide

schering pty ltd - acephate - insecticide - broccoli | brussels sprouts | cabbage | cauliflower | macadamia nut | ornamental | potato | tobacco | tomato | carnation | chrys - aphid | banana spotting bug | cabbage aphid | cabbage moth | cabbage white butterfly | cluster caterpillar | flower thrip | fruitspotting bug - amblypelta nitida | helicoverpa spp. | leafminer flies | macadamia flower caterpillar | macadamia leafminer | macadamia nutborer | potato moth or tobacco leafminer | redshouldered leaf beetle | tobacco budworm | tobacco looper or looper caterpillar | tobacco stem borer | whitefly | corn earworm | cotton bollworm | diamondback moth | grey cabbage aphid | heliothis | leafminers | macadamia flower thrips | monolepta beetle | native budworm | potato tuber moth | red shouldered leaf beetle | stem borer | tobacco budworm | tobacco leafminer | tomato grub

SCHERING CARBARYL 800 W INSECTICIDE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

schering carbaryl 800 w insecticide

schering pty ltd - carbaryl - insecticide - apple crop = apple orchard | apricot | cereal crop | citrus fruit or tree | field crop | grapevine | lucerne pasture - refer to - codling moth | cutworm - agrotis spp. | european earwig | fruit thinning | grapeleaf blister mite | grapevine hawk moth | grapevine moth | green vegetable bug | large leafeating ladybird | light brown apple moth | looper | lucerne leafroller | native budworm or bollworm | orange fruit borer | oriental fruit moth | pear and cherry slug | pearleaf blister mite | potato moth | pumpkin beetle | sitona weevil | spined or larger horned citrus bug | tobacco leafminer | treehopper | wingless grasshopper | yellow peach moth | eriophyes pyri | fruit thinning | heliothis | looper caterpillars | native bollworm | potato moth | potato tuber moth | tobacco leafminer | vineleaf blister mite