cardiorytmin 100 mg ml injection - search results

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

hospira vincristine sulfate injection usp 2 mg/2 ml vial

hospira australia pty ltd - vincristine sulfate, quantity: 1 mg/ml - injection - excipient ingredients: water for injections; mannitol; sodium hydroxide; sulfuric acid - vincristine sulfate injection is indicated in acute leukemia. vincristine sulfate injection has also been shown to be useful in combination with other oncolytic agents in hodgkin's disease, non-hodgkin's malignant lymphomas (lymphocytic, mixed cell, histiocytic, undifferentiated, nodular and diffuse types), rhabdomyosarcoma, neuroblastoma, and wilm's tumor.

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

nepexto etanercept 50 mg/1 ml solution for injection auto-injector

maxx pharma pty ltd - etanercept, quantity: 50 mg - injection, solution - excipient ingredients: water for injections; sodium chloride; glycine; sucrose; sodium citrate dihydrate; monobasic sodium phosphate dihydrate - nepexto is indicated for the treatment of:,adults,rheumatoid arthritis,active, adult rheumatoid arthritis (ra) in patients who have had inadequate response to one or more disease-modifying antirheumatic drugs (dmards). nepexto can be used in combination with methotrexate.,severe, active rheumatoid arthritis in adults to slow progression of disease-associated structural damage in patients at high risk of erosive disease.,psoriatic arthritis,the signs and symptoms of active and progressive psoriatic arthritis in adults, when the response to previous disease-modifying antirheumatic therapy has been inadequate. etanercept has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function.,plaque psoriasis,adult patients with moderate to severe chronic plaque psoriasis, who are candidates for phototherapy or systemic therapy.,ankylosing spondylitis,the signs and symptoms of active ankylosing spondylitis in adults.,non-radiographic axial spondyloarthritis,treatment of adults with active* non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or mri change who have had an inadequate response to nsaids.,* active disease is defined as a bath ankylosing spondylitis disease activity index (basdai) score of >= 4.,children and adolescents,children and adolescents weighing less than 62.5 kg should not receive nepexto. these patients should be accurately dosed on a mg/kg basis with other etanercept products.,juvenile idiopathic arthritis,active polyarthritis (rheumatoid factor positive or negative) in children and adolescents, aged 2 to 17 years, who have had an inadequate response to one or more dmards.,active extended oligoarthritis in children and adolescents, aged 2 to 17 years, who have had an inadequate response to, or who have proved intolerant to, methotrexate.,active enthesitis-related arthritis in adolescents, aged 12 to 17 years, who have had an inadequate response to, or who have proved intolerant to, conventional therapy.,active psoriatic arthritis in adolescents, aged 12 to 17 years, who have had an inadequate response to, or who have proved intolerant to, methotrexate.,etanercept has not been studied in children aged less than 2 years.,paediatric plaque psoriasis,chronic, severe plaque psoriasis in children and adolescents from 4 to 17 years, who are inadequately controlled by, or are intolerant to, other systemic therapies or phototherapies. duration of therapy to be no longer than 24 weeks and treatment to be ceased after 12 weeks if a significant psoriasis area and severity index (pasi) response is not achieved.

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

doxorubicin 50mg/25ml solution for injection cytosafe vials

pfizer ltd - doxorubicin hydrochloride - solution for injection - 2mg/1ml

New Zealand - English - Medsafe (Medicines Safety Authority)

penicillin g sodium injection

sandoz new zealand limited - benzylpenicillin sodium 600mg equivalent to benzylpenicillin 1,000,000 iu (sterile) - powder for injection - 1e+006 iu - active: benzylpenicillin sodium 600mg equivalent to benzylpenicillin 1,000,000 iu (sterile)

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

enbrel 25mg powder and solvent for solution for injection vials

pfizer ltd - etanercept - powder and solvent for solution for injection - 25mg

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

enbrel 50mg1ml solution for injection pre-filled syringes

pfizer ltd - etanercept - solution for injection - 50mg/1ml

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

enbrel 25mg0.5ml solution for injection pre-filled syringes

pfizer ltd - etanercept - solution for injection - 50mg/1ml