ZYTIGA abiraterone acetate 500 mg film-coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

zytiga abiraterone acetate 500 mg film-coated tablet blister pack

janssen-cilag pty ltd - abiraterone acetate, quantity: 500 mg - tablet, film coated - excipient ingredients: lactose monohydrate; croscarmellose sodium; sodium lauryl sulfate; silicified microcrystalline cellulose; hypromellose; magnesium stearate; silicon dioxide; titanium dioxide; purified talc; iron oxide red; polyvinyl alcohol; macrogol 3350; iron oxide black - zytiga is indicated in combination with prednisone or prednisolone for the treatment of: ? newly diagnosed high-risk metastatic hormone sensitive prostate cancer (mhspc) in combination with androgen deprivation therapy (adt), or ? patients with metastatic advanced prostate cancer (castration resistant prostate cancer, mcrpc) who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy (adt) or ? patients with mcrpc who have received prior chemotherapy containing a taxane.

Global Advantage CTA Heads - Prosthesis, internal, joint, shoulder, humeral component Australia - English - Department of Health (Therapeutic Goods Administration)

global advantage cta heads - prosthesis, internal, joint, shoulder, humeral component

johnson & johnson medical pty ltd t/a depuy synthes - 48088 - humeral head prosthesis - global advantage cta heads are designed to replace the humeral head of the shoulder. it is made of cobalt chrome, and is attached to a humeral stem prosthesis and articulates with the natural glenoid fossa. it has an extended humeral head design which creates a larger area of lateral articulation. the cta head provides a greater area of articulation in abduction and also in external rotation. global advantage cta heads are intended for hemi-shoulder replacement. hemi-shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon?s experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). 4.

METARAMINOL PHEBRA metaraminol (as tartrate) 3mg/6mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

metaraminol phebra metaraminol (as tartrate) 3mg/6ml injection vial

phebra pty ltd - metaraminol tartrate, quantity: 5.7 mg - injection - excipient ingredients: sodium chloride; sodium metabisulfite; water for injections; sodium hydroxide; tartaric acid - prevention and treatment of the acute hypotensive state occurring with spinal anaesthesia; adjunctive treatment of hypotension due to haemorrhage, reactions to medications, surgical complications, and shock associated with brain damage due to tumour or trauma.,it may also be useful as an adjunct in the treatment of hypotension due to cardiogenic shock or septicaemia.

METARAMINOL PHEBRA metaraminol (as tartrate) 5mg/10mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

metaraminol phebra metaraminol (as tartrate) 5mg/10ml injection vial

phebra pty ltd - metaraminol tartrate, quantity: 9.5 mg - injection - excipient ingredients: sodium chloride; water for injections; sodium metabisulfite; sodium hydroxide; tartaric acid - prevention and treatment of the acute hypotensive state occurring with spinal anaesthesia; adjunctive treatment of hypotension due to haemorrhage, reactions to medications, surgical complications, and shock associated with brain damage due to tumour or trauma.,it may also be useful as an adjunct in the treatment of hypotension due to cardiogenic shock or septicaemia.