België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

teva pharma belgium sa-nv - vinblastinesulfaat 1 mg/ml - oplossing voor injectie - 1 mg/ml - vinblastinesulfaat 1 mg/ml - vinblastine

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sandoz sa-nv - vinorelbinetartraat 13,85 mg/ml - eq. vinorelbine 10 mg/ml - concentraat voor oplossing voor infusie - 10 mg/ml - vinorelbinetartraat 13.85 mg/ml - vinorelbine

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sandoz sa-nv - vinorelbinetartraat 13,85 mg/ml - eq. vinorelbine 10 mg/ml - concentraat voor oplossing voor infusie - 10 mg/ml - vinorelbinetartraat 13.85 mg/ml - vinorelbine

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

eureco-pharma b.v. boelewerf 2 2987 vd ridderkerk - oxytocine 5 ie/ml - oplossing voor injectie of infusie - azijnzuur (e 260), geconcentreerd ; natriumacetaat 3-water (e 262) ; natriumchloride ; water voor injectie

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

medac gmbh - mitomycine 2 mg - poeder voor oplossing voor intravesicaal gebruik/injectie/infusie - 1 mg/ml - mitomycine 10 mg - mitomycin

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

medac gmbh - mitomycine 2 mg - poeder voor oplossing voor intravesicaal gebruik/injectie/infusie - 1 mg/ml - mitomycine 20 mg - mitomycin

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

medac gmbh - mitomycine 2 mg - poeder voor oplossing voor intravesicaal gebruik/injectie/infusie - 1 mg/ml - mitomycine 2 mg - mitomycin

België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

medac gmbh - mitomycine 2 mg - poeder voor oplossing voor intravesicaal gebruik/injectie/infusie - 1 mg/ml - mitomycine 40 mg - mitomycin

Europese Unie - Nederlands - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir - hiv-infecties - antivirale middelen voor systemisch gebruik - prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adult and paediatric patients from the age of 3 years and at least 15 kg body weight. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). in deciding to initiate treatment with prezista co administered with cobicistat or low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista 75 mg, 150 mg, and 600 mg tablets may be used to provide suitable dose regimens:for the treatment of hiv 1 infection in antiretroviral treatment (art) experienced adult patients, including those that have been highly pre treated. for the treatment of hiv 1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. in deciding to initiate treatment with prezista co administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). prezista 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv 1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are:antiretroviral therapy (art) naïve. art experienced with no darunavir resistance associated mutations (drv rams) and who have plasma hiv 1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 106/l. in deciding to initiate treatment with prezista in such art experienced patients, genotypic testing should guide the use of prezista.

Europese Unie - Nederlands - EMA (European Medicines Agency)

astrazeneca ab - ticagrelor - peripheral vascular diseases; acute coronary syndrome - antitrombotische middelen - possia, samen met acetylsalicylzuur (asa), beheerd is geïndiceerd voor de preventie van atherotrombotische gebeurtenissen bij volwassen patiënten met acute coronaire syndromen (unstable angina pectoris, niet-st-elevatie myocardinfarct [nstemi] of st-elevatie myocardiaal infarct [stemi]); patiënten die medisch beheerd alsmede, degenen die worden beheerd met percutane coronaire interventie (pci) of coronaire by-pass enten (cabg).