Joflupaan (123I) Rotop 74 MBq/ml inj. sol. i.v. vial Belgija - anglų - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

joflupaan (123i) rotop 74 mbq/ml inj. sol. i.v. vial

rotop radiopharmacy gmbh - sodium iodide (123 i) 74 mbq/ml - solution for injection - 74 mbq/ml - ioflupane (i-123) 74 mbq/ml - iodine ioflupane (123i)

DATSCAN SOLUTION Kanada - anglų - Health Canada

datscan solution

ge healthcare canada inc - ioflupane (123i) - solution - 74mbq - ioflupane (123i) 74mbq - roentgenography

DATSCAN SOLUTION FOR INJECTION 74 MBQML Singapūras - anglų - HSA (Health Sciences Authority)

datscan solution for injection 74 mbqml

ge healthcare pte. ltd. - ioflupane (123i) - injection, solution - ioflupane (123i) 74 mbq/ml at reference time

MIBGen Australija - anglų - Department of Health (Therapeutic Goods Administration)

mibgen

ansto t/a ansto health - iobenguane(123i) sulfate; iobenguane [123i] sulfate; iobenguane sulfate [123i] -

Exelon Patch 10 Naujoji Zelandija - anglų - Medsafe (Medicines Safety Authority)

exelon patch 10

novartis new zealand ltd - rivastigmine 18mg;  ;   - transdermal patch - 9.5 mg/24h - active: rivastigmine 18mg     excipient: dimeticone dl-alpha tocopherol acrylic pressure sensitive adhesive silicone pressure sensitive adhesive backing film 10 cm square release liner 20.25 cm square poly(butyl methacrylate-co-methyl methacrylate) - treatment of patients with: · mild to moderately severe dementia of the alzheimer's type (also termed probable alzheimer's disease or alzheimer's disease) · severe dementia of the alzheimer's type.

Exelon Patch 15 Naujoji Zelandija - anglų - Medsafe (Medicines Safety Authority)

exelon patch 15

novartis new zealand ltd - rivastigmine 27mg;  ;   - transdermal patch - 13.3 mg/24h - active: rivastigmine 27mg     excipient: dimeticone dl-alpha tocopherol acrylic pressure sensitive adhesive silicone pressure sensitive adhesive backing film 15 cm square release liner 30.375 cm square poly(butyl methacrylate-co-methyl methacrylate) - treatment of patients with: · mild to moderately severe dementia of the alzheimer's type (also termed probable alzheimer's disease or alzheimer's disease) · severe dementia of the alzheimer's type.

Exelon Patch 5 Naujoji Zelandija - anglų - Medsafe (Medicines Safety Authority)

exelon patch 5

novartis new zealand ltd - rivastigmine 9mg;  ;   - transdermal patch - 4.6 mg/24h - active: rivastigmine 9mg     excipient: dimeticone dl-alpha tocopherol acrylic pressure sensitive adhesive silicone pressure sensitive adhesive backing film 5 cm square release liner 10.125 cm square poly(butyl methacrylate-co-methyl methacrylate) - treatment of patients with: · mild to moderately severe dementia of the alzheimer's type (also termed probable alzheimer's disease or alzheimer's disease) · severe dementia of the alzheimer's type.

Simulect Naujoji Zelandija - anglų - Medsafe (Medicines Safety Authority)

simulect

novartis new zealand ltd - basiliximab 10mg (murine/human; formulated with a 7.5% total overage);   - powder for injection - 10 mg - active: basiliximab 10mg (murine/human; formulated with a 7.5% total overage)   excipient: dibasic sodium phosphate glycine mannitol monobasic potassium phosphate sodium chloride sucrose water for injection - simulect is indicated for the prophylaxis of acute organ rejection in de novo renal transplantation in adult and paediatric patients. it is to be used concomitantly with cyclosporin for microemulsion- and corticosteroid-based immunosuppression or in a triple maintenance immunosuppressive regimen containing cyclosporin for microemulsion, corticosteroids and either azathioprine or mycophenolate mofetil.

Simulect Naujoji Zelandija - anglų - Medsafe (Medicines Safety Authority)

simulect

novartis new zealand ltd - basiliximab 20mg (murine/human; formulated with a 7.5% total overage) - powder for injection - 20 mg - active: basiliximab 20mg (murine/human; formulated with a 7.5% total overage) excipient: dibasic sodium phosphate glycine mannitol monobasic potassium phosphate sodium chloride sucrose water for injection - simulect is indicated for the prophylaxis of acute organ rejection in de novo renal transplantation in adult and paediatric patients. it is to be used concomitantly with cyclosporin for microemulsion- and corticosteroid-based immunosuppression or in a triple maintenance immunosuppressive regimen containing cyclosporin for microemulsion, corticosteroids and either azathioprine or mycophenolate mofetil.