Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

bayer australia ltd - octocog alfa, quantity: 3000 iu - injection, diluent for - excipient ingredients: water for injections - kogenate fs is indicated for the treatment and prophylaxis of bleeding in patients with haemophilia a (congenital factor viii deficiency). it may also be used in patients with factor viii inhibitors (neutralising antibodies) who continue to respond to infused factor viii. kogenate fs does not contain von willebrand factor and hence is not indicated in von willebrands disease.

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

glaxosmithkline australia pty ltd - rubella virus, quantity: 1000 ccid50; mumps virus, quantity: 5000 ccid50; measles virus, quantity: 1000 ccid50 - diluent, not applicable - excipient ingredients: water for injections - priorix is indicated for active immunisation against measles, mumps and rubella from 12 months of age.

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

csl behring australia pty ltd - factor viii, quantity: 500 iu; von willebrand factor, quantity: 1200 iu - injection, diluent for - excipient ingredients: - the prophylaxis and treatment of non-surgical and surgical bleeding in patients with von willebrand disease when desmopressin (ddavp) treatment is ineffective or contraindicated. the prophylaxis and treatment of non-surgical and surgical bleeding associated with factor viii deficiency due to haemophilia a.

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

csl behring australia pty ltd - factor viii, quantity: 250 iu; von willebrand factor, quantity: 600 iu - injection, diluent for - excipient ingredients: - the prophylaxis and treatment of non-surgical and surgical bleeding in patients with von willebrand disease when desmopressin (ddavp) treatment is ineffective or contraindicated. the prophylaxis and treatment of non-surgical and surgical bleeding associated with factor viii deficiency due to haemophilia a.

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

merck sharp & dohme (australia) pty ltd - water for injections, quantity: 0.75 ml - diluent, not applicable - excipient ingredients: - for use as a diluent for merck, sharp & dohme live virus vaccines.

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

novo nordisk pharmaceuticals pty ltd - glucagon, quantity: 1 mg (equivalent: glucagon, qty 1 iu) - diluent, not applicable - excipient ingredients: water for injections - therapeutic: treatment of severe hypoglycaemic reactions which may occur in the management of diabetic patients receiving insulin or oral hypoglycaemic agents. to prevent the occurrence of secondary hypoglycaemia, oral carbohydrate should be given to restore the hepatic glycogen when the patient has responded to the treatment. the mechanism and hence treatment of sulfonylurea-induced hypoglycaemia differs from that of severe insulin-induced hypoglycaemia in some important ways. consciousness should preferably be restored by the administration of intravenous glucose. if glucagon is used due to the unavailability of intravenous glucose (e.g. before reaching a hospital) care should be taken to protect against secondary hypoglycaemia with constant monitoring of the patient's blood sugar level by medical personnel. subsequent administration of intravenous glucose may be required.,diagnostic: motility inhibitor in examinations of the gastrointestinal tract in adults, e.g. double contrast radiography and endoscop

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

servier laboratories (aust) pty ltd - fotemustine, quantity: 208 mg - diluent, not applicable - excipient ingredients: water for injections; ethanol - disseminated malignant melanoma, including cerebral metastases, administered alone or in combination with other cancer agents.

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

emcure pharmaceuticals pty ltd - melphalan hydrochloride, quantity: 55.97 mg (equivalent: melphalan, qty 50 mg) - injection, diluent for - excipient ingredients: sodium citrate dihydrate; ethanol; water for injections; propylene glycol - for?the?treatment?of?patients?with?multiple?myeloma?for?whom?oral therapy?is?not?appropriate

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

reach pharmaceuticals pty ltd - cabazitaxel, quantity: 60 mg - injection, diluent for - excipient ingredients: ethanol; water for injections - msn cabazitaxel in combination with prednisone or prednisolone is indicated for the treatment of patients with metastatic castration resistant prostate cancer previously treated with a docetaxel containing regimen.

Euroopa Liit - malta - EMA (European Medicines Agency)

pfizer limited - difloxacin - antibatteriċi għal użu sistemiku, antiinfectives għall-użu sistemiku - turkeys; dogs; cattle; chicken - tiġieġ:għat-trattament ta 'infezzjonijiet kroniċi respiratorji kkawżati minn strejns sensittivi ta' eschericia coli u mycoplasma gallisepticum. dundjani: għall-kura ta 'infezzjonijiet respiratorji kroniċi kkawżati minn razez sensittivi ta' escherichia coli u mycoplasma gallisepticum. ukoll għat-trattament ta 'infezzjonijiet ikkawżati minn pasteurella multocida. klieb: għat-trattament ta 'infezzjonijiet akuti mhux ikkomplikati ta' l-apparat urinarju kkawżati minn escherichia coli jew staphylococcus spp. u pyoderma superfiċjali kkawżata minn staphylococcus intermedius. baqar:għat-trattament tal-marda respiratorja bovina (shipping fever, pnewmonja fl-għoġliet) kkawżata minn doża waħda jew infezzjonijiet imħalta ma ' pasteurella haemolytica, pasteurella multocida, u / jew mycoplasma spp.