European Union - English - EMA (European Medicines Agency)

schering-plough europe - posaconazole - candidiasis; mycoses; coccidioidomycosis; aspergillosis - antimycotics for systemic use - posaconazole sp is indicated for use in the treatment of the following fungal infections in adults (see section 5.1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products;- oropharyngeal candidiasis: as first-line therapy in patients who have severe disease or are immunocompromised, in whom response to topical therapy is expected to be poor.refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy.posaconazole sp is also indicated for prophylaxis of invasive fungal infections in the following patients:- patients receiving remission-induction chemotherapy for acute myelogenous leukemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who areat high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections.

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

pharmacor pty ltd - pregabalin, quantity: 25 mg - capsule, hard - excipient ingredients: purified talc; titanium dioxide; gelatin; pregelatinised maize starch; sodium lauryl sulfate; purified water; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - neuroccord (pregabalin) is indicated for the treatment of neuropathic pain in adults.,neuroccord (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

pharmacor pty ltd - pregabalin, quantity: 300 mg - capsule, hard - excipient ingredients: gelatin; purified talc; sodium lauryl sulfate; purified water; titanium dioxide; pregelatinised maize starch; iron oxide red; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - neuroccord (pregabalin) is indicated for the treatment of neuropathic pain in adults.,neuroccord (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

pharmacor pty ltd - pregabalin, quantity: 300 mg - capsule, hard - excipient ingredients: gelatin; purified talc; pregelatinised maize starch; titanium dioxide; iron oxide red; sodium lauryl sulfate; purified water; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - neuroccord (pregabalin) is indicated for the treatment of neuropathic pain in adults.,neuroccord (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

pharmacor pty ltd - pregabalin, quantity: 75 mg - capsule, hard - excipient ingredients: gelatin; titanium dioxide; iron oxide red; sodium lauryl sulfate; purified talc; purified water; pregelatinised maize starch; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - neuroccord (pregabalin) is indicated for the treatment of neuropathic pain in adults.,neuroccord (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

pharmacor pty ltd - pregabalin, quantity: 75 mg - capsule, hard - excipient ingredients: gelatin; pregelatinised maize starch; titanium dioxide; purified talc; iron oxide red; sodium lauryl sulfate; purified water; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - neuroccord (pregabalin) is indicated for the treatment of neuropathic pain in adults.,neuroccord (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

pharmacor pty ltd - pregabalin, quantity: 25 mg - capsule, hard - excipient ingredients: sodium lauryl sulfate; purified water; purified talc; gelatin; titanium dioxide; pregelatinised maize starch; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - neuroccord (pregabalin) is indicated for the treatment of neuropathic pain in adults.,neuroccord (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

pharmacor pty ltd - pregabalin, quantity: 150 mg - capsule, hard - excipient ingredients: titanium dioxide; gelatin; purified talc; sodium lauryl sulfate; purified water; pregelatinised maize starch; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - neuroccord (pregabalin) is indicated for the treatment of neuropathic pain in adults.,neuroccord (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

pharmacor pty ltd - pregabalin, quantity: 150 mg - capsule, hard - excipient ingredients: gelatin; sodium lauryl sulfate; purified water; titanium dioxide; purified talc; pregelatinised maize starch; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - neuroccord (pregabalin) is indicated for the treatment of neuropathic pain in adults.,neuroccord (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

alphapharm pty ltd - tramadol hydrochloride -