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

roche products pty ltd - vismodegib, quantity: 150 mg - capsule, hard - excipient ingredients: purified talc; iron oxide red; gelatin; sodium starch glycollate; microcrystalline cellulose; titanium dioxide; iron oxide black; shellac; lactose monohydrate; povidone; magnesium stearate; sodium lauryl sulfate - erivedge is indicated for the treatment of adult patients with metastatic basal cell carcinoma, or with locally advanced basal cell carcinoma where surgery and/or radiation therapy are not appropriate.

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

roche products pty ltd - oseltamivir phosphate, quantity: 59.1 mg (equivalent: oseltamivir, qty 45 mg) - capsule, hard - excipient ingredients: povidone; croscarmellose sodium; purified talc; sodium stearylfumarate; pregelatinised maize starch; titanium dioxide; purified water; iron oxide yellow; iron oxide red; gelatin; iron oxide black; indigo carmine; butan-1-ol; ethanol; shellac; methanol - tamiflu is indicated for the treatment of infections due to influenza a and b viruses in adults and children including full-term neonates. treatment should commence as soon as possible, but no later than 48 hours after the onset of the initial symptoms of infection.,tamiflu is indicated for the prevention of influenza in adults and children aged 1 year and older. vaccination is the preferred method of routine prophylaxis against infection with influenza virus.

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

roche products pty ltd - oseltamivir phosphate, quantity: 39.4 mg (equivalent: oseltamivir, qty 30 mg) - capsule, hard - excipient ingredients: povidone; croscarmellose sodium; purified talc; sodium stearylfumarate; pregelatinised maize starch; titanium dioxide; purified water; iron oxide yellow; iron oxide red; gelatin; iron oxide black; indigo carmine; butan-1-ol; ethanol; shellac; methanol - tamiflu is indicated for the treatment of infections due to influenza a and b viruses in adults and children including full-term neonates. treatment should commence as soon as possible, but no later than 48 hours after the onset of the initial symptoms of infection.,tamiflu is indicated for the prevention of influenza in adults and children aged 1 year and older. vaccination is the preferred method of routine prophylaxis against infection with influenza virus.

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

roche products pty ltd - saquinavir mesilate, quantity: 571.5 mg (equivalent: saquinavir, qty 500 mg) - tablet, film coated - excipient ingredients: microcrystalline cellulose; povidone; triacetin; croscarmellose sodium; titanium dioxide; hypromellose; purified talc; iron oxide red; lactose monohydrate; iron oxide yellow; magnesium stearate - invirase (saquinavir) is indicated for the treatment of hiv/aids in adults and children 12 years of age or older. clinical studies indicate that saquinavir should only be used in combination with ritonavir and other anti-retroviral therapies (see clinical trials). this indication is based on changes in surrogate markers. at present there are no results from controlled clinical trials evaluating the effect of regimens containing saquinavir on hiv disease progression or survival (see clinical trials).

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

roche products pty ltd - sulfamethoxazole,trimethoprim -

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

roche products pty ltd - bevacizumab, quantity: 400 mg - injection, concentrated - excipient ingredients: water for injections; monobasic sodium phosphate monohydrate; trehalose dihydrate; polysorbate 20; dibasic sodium phosphate heptahydrate - ? metastatic colorectai cancer avastin (bevacizumab) in combination with fluoropyrimidine-based chemotherapy is indicated for the treatment of patients with metastatic colorectal cancer. ? locally recurrent or metastatic breast cancer avastin (bevacizumab) in combination with paclitaxel is indicated for the first-line treatment of metastatic breast cancer in patients in whom an anthracycline-based therapy is contraindicated.(see clinical trials). ? advanced, metastatic or recurrent non-squamous non-small cell lung cancer (nsclc) avastin (bevacizumab), in combination with carboplatin and paclitaxel, is indicated for first-line treatment of patients with unresectable advanced, metastatic or recurrent, non-squamous non-small cell lung cancer. ? advanced and/or metastatic renai cell cancer avastin (bevacizumab) in combination with interferon alfa-2a is indicated for treatment of patients with advanced and/or metastatic renal cell cancer ? grade iv glioma avastin (bevacizumab) as a single agent, is indicated for t

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

roche products pty ltd - bevacizumab, quantity: 100 mg - injection, concentrated - excipient ingredients: monobasic sodium phosphate monohydrate; water for injections; polysorbate 20; trehalose dihydrate; dibasic sodium phosphate heptahydrate - ? metastatic colorectai cancer avastin (bevacizumab) in combination with fluoropyrimidine-based chemotherapy is indicated for the treatment of patients with metastatic colorectal cancer. ? locally recurrent or metastatic breast cancer avastin (bevacizumab) in combination with paclitaxel is indicated for the first-line treatment of metastatic breast cancer in patients in whom an anthracycline-based therapy is contraindicated.(see clinical trials). ? advanced, metastatic or recurrent non-squamous non-small cell lung cancer (nsclc) avastin (bevacizumab), in combination with carboplatin and paclitaxel, is indicated for first-line treatment of patients with unresectable advanced, metastatic or recurrent, non-squamous non-small cell lung cancer. ? advanced and/or metastatic renai cell cancer avastin (bevacizumab) in combination with interferon alfa-2a is indicated for treatment of patients with advanced and/or metastatic renal cell cancer ? grade iv glioma avastin (bevacizumab) as a single agent, is indicated for t

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

roche products pty ltd - mycophenolate mofetil, quantity: 500 mg - tablet, film coated - excipient ingredients: croscarmellose sodium; purified talc; povidone; microcrystalline cellulose; magnesium stearate; titanium dioxide; hypromellose; indigo carmine; hyprolose; iron oxide red; macrogol 400 - cellcept is indicated for the prophylaxis of solid organ rejection in adults receiving allogeneic organ transplants. cellcept is indicated for the prophylaxis of organ rejection in paediatric patients (2 to 18 years) receiving allogeneic renal transplants.

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

roche products pty ltd - oseltamivir phosphate, quantity: 98.5 mg (equivalent: oseltamivir, qty 75 mg) - capsule, hard - excipient ingredients: pregelatinised maize starch; purified talc; povidone; croscarmellose sodium; sodium stearylfumarate; titanium dioxide; purified water; iron oxide yellow; iron oxide red; gelatin; iron oxide black; indigo carmine; butan-1-ol; ethanol; shellac; methanol - tamiflu is indicated for the treatment of infections due to influenza a and b viruses in adults and children including full-term neonates. treatment should commence as soon as possible, but no later than 48 hours after the onset of the initial symptoms of infection.,tamiflu is indicated for the prevention of influenza in adults and children aged 1 year and older. vaccination is the preferred method of routine prophylaxis against infection with influenza virus.

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

roche products pty ltd - mycophenolate mofetil, quantity: 250 mg - capsule, hard - excipient ingredients: povidone; titanium dioxide; iron oxide yellow; iron oxide red; croscarmellose sodium; gelatin; pregelatinised maize starch; indigo carmine; magnesium stearate - cellcept is indicated for the prophylaxis of solid organ rejection in adults receiving allogeneic organ transplants. cellcept is indicated for the prophylaxis of organ rejection in paediatric patients (2 to 18 years) receiving allogeneic renal transplants.