FIRMAGON degarelix (as acetate) composite pack of 80mg powder in vial and solvent for injection in pre-filled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

firmagon degarelix (as acetate) composite pack of 80mg powder in vial and solvent for injection in pre-filled syringe

ferring pharmaceuticals pty ltd - water for injections, quantity: 4.2 ml - injection - excipient ingredients: - firmagon is a gnrh receptor blocker indicated for treatment of patients with prostate cancer in whom androgen deprivation is warranted.

FIRMAGON degarelix (as acetate) composite 120 mg powder in vial and solvent for injection in pre-filled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

firmagon degarelix (as acetate) composite 120 mg powder in vial and solvent for injection in pre-filled syringe

ferring pharmaceuticals pty ltd - water for injections, quantity: 3 ml - injection - excipient ingredients: - firmagon is a gnrh receptor blocker indicated for treatment of patients with prostate cancer in whom androgen deprivation is warranted.

DIPHERELINE triptorelin (as embonate) 22.5 mg powder for suspension vial and water for injections ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

diphereline triptorelin (as embonate) 22.5 mg powder for suspension vial and water for injections ampoule

ipsen pty ltd - triptorelin embonate, quantity: 31 mg (equivalent: triptorelin, qty 22.5 mg) - suspension, powder for - excipient ingredients: polyglactin; carmellose sodium; polysorbate 80; mannitol - diphereline is indicated for the treatment of hormone-dependent locally advanced or metastatic prostate cancer.,diphereline 22.5mg 6 month formulation only:,diphereline 22.5 mg is indicated for the treatment of children 2 years and older with central precocious puberty (cpp).

BERINERT IV human C1 esterase inhibitor 500 IU powder for injection vial with diluent vial Australia - English - Department of Health (Therapeutic Goods Administration)

berinert iv human c1 esterase inhibitor 500 iu powder for injection vial with diluent vial

csl behring australia pty ltd - water for injections, quantity: 10 ml - injection, diluent for - excipient ingredients: - berinert iv is indicated for the treatment of acute attacks in patients with hereditary angioedema (hae).

BERIPLEX P/N human prothrombin complex 500 IU powder for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

beriplex p/n human prothrombin complex 500 iu powder for injection vial

csl behring australia pty ltd - water for injections, quantity: 20 ml - injection, solution - excipient ingredients: - treatment and perioperative prophylaxis of bleedings in acquired deficiency of the prothrombin complex coagulation factors, such as deficiency caused by treatment with vitamin k antagonists, or in case of overdose of vitamin k antagonists, when rapid correction of the deficiency is required.

DIPHERELINE triptorelin {as embonate} 11.25mg powder for suspension vial and water for injections ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

diphereline triptorelin {as embonate} 11.25mg powder for suspension vial and water for injections ampoule

ipsen pty ltd - triptorelin embonate, quantity: 19.32 mg - injection, diluent for - excipient ingredients: water for injections - diphereline is indicated for the treatment of hormone-dependent locally advanced or metastatic prostate cancer.

DIPHERELINE triptorelin (as embonate) 3.75 mg powder for suspension vial and water for injections ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

diphereline triptorelin (as embonate) 3.75 mg powder for suspension vial and water for injections ampoule

ipsen pty ltd - triptorelin embonate, quantity: 5.6 mg (equivalent: triptorelin, qty 3.75 mg) - injection, diluent for - excipient ingredients: water for injections - diphereline is indicated for the treatment of hormone-dependent locally advanced or metastatic prostate cancer.

SMOFKABIVEN LOW OSMO amino acids 2.5%, electrolytes 0.4%, lipids 3.5% & glucose 6.8% emulsion for intravenous infusion 2500 mL biofine bag Australia - English - Department of Health (Therapeutic Goods Administration)

smofkabiven low osmo amino acids 2.5%, electrolytes 0.4%, lipids 3.5% & glucose 6.8% emulsion for intravenous infusion 2500 ml biofine bag

fresenius kabi australia pty ltd - fish oil - rich in omega-3 acids, quantity: 30 g/l; medium chain triglycerides, quantity: 60 g/l; olive oil, quantity: 50 g/l; soya oil, quantity: 60 g/l - injection, intravenous infusion - excipient ingredients: dl-alpha-tocopherol; egg lecithin; glycerol; sodium oleate; sodium hydroxide; water for injections - parenteral nutrition for adult patients and paediatric patients aged 2 years and above when oral or enteral nutrition is impossible, insufficient or contraindicated.

SMOFlipid (lipid emulsion) 20% emulsion for intravenous infusion 500 mL bag Australia - English - Department of Health (Therapeutic Goods Administration)

smoflipid (lipid emulsion) 20% emulsion for intravenous infusion 500 ml bag

fresenius kabi australia pty ltd - olive oil, quantity: 50 g; fish oil - rich in omega-3 acids, quantity: 30 g; medium chain triglycerides, quantity: 60 g; soya oil, quantity: 60 g - injection, intravenous infusion - excipient ingredients: glycerol; sodium oleate; dl-alpha-tocopherol; water for injections; egg lecithin; sodium hydroxide - supply of energy and essential fatty acids to patients, as part of a parenteral nutrition regimen, when oral or enteral nutrition is impossible, insufficient or contra-indicated.

GLAMIN amino acids/dipeptides 500mL intravenous   infusion injection bottle Australia - English - Department of Health (Therapeutic Goods Administration)

glamin amino acids/dipeptides 500ml intravenous infusion injection bottle

fresenius kabi australia pty ltd - proline, quantity: 6.8 g/l; isoleucine, quantity: 5.6 g/l; methionine, quantity: 5.6 g/l; lysine acetate, quantity: 12.7 g/l (equivalent: lysine, qty 9 g; equivalent: glycine, qty 10.27 g); serine, quantity: 4.5 g/l; glycylglutamine monohydrate, quantity: 30.27 g/l (equivalent: glycine, qty 10.27 g; equivalent: glutamine, qty 20 g); alanine, quantity: 16 g/l; histidine, quantity: 6.8 g/l; glutamic acid, quantity: 5.6 g/l; tryptophan, quantity: 1.9 g/l; leucine, quantity: 7.9 g/l; valine, quantity: 7.3 g/l; aspartic acid, quantity: 3.4 g/l; phenylalanine, quantity: 5.85 g/l; glycyltyrosine dihydrate, quantity: 3.45 g/l (equivalent: tyrosine, qty 2.28 g; equivalent: glycine, qty 0.94 g); arginine, quantity: 11.3 g/l; threonine, quantity: 5.6 g/l - injection, intravenous infusion - excipient ingredients: citric acid; water for injections - glamin provides amino acids as part of parenteral nutrition therapy, when oral or enteral nutrition is impossible, insufficient or contraindicated especially in patients with a moderate or severe catabolic status.