Portugāle - portugāļu - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

neuraxpharm spain, s.l.u. - aripiprazol - comprimido - 10 mg - aripiprazol 10 mg - aripiprazole - genérico - duração do tratamento: longa duração

Portugāle - portugāļu - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

neuraxpharm spain, s.l.u. - aripiprazol - comprimido - 30 mg - aripiprazol 30 mg - aripiprazole - genérico - duração do tratamento: longa duração

Portugāle - portugāļu - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

neuraxpharm spain, s.l.u. - aripiprazol - comprimido - 30 mg - aripiprazol 30 mg - aripiprazole - genérico - duração do tratamento: longa duração

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - avatrombopag maleate - trombocitopenia - anti-hemorrágicos - doptelet é indicado para o tratamento da trombocitopenia grave em doentes adultos com doença crônica do fígado, que são programados para se submeter a um procedimento invasivo. doptelet is indicated for the treatment of primary chronic immune thrombocytopenia (itp) in adult patients who are refractory to other treatments (e. corticosteróides, imunoglobulinas).

Portugāle - portugāļu - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

mylan, lda. - desogestrel - comprimido - 0.075 mg - desogestrel 0.075 mg - desogestrel - genérico - duração do tratamento: longa duração

Portugāle - portugāļu - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

mylan, lda. - desogestrel - comprimido - 0.075 mg - desogestrel 0.075 mg - desogestrel - genérico - duração do tratamento: longa duração

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

les laboratoires servier - irinotecan anhydrous free-base - neoplasias pancreáticas - agentes antineoplásicos - tratamento do adenocarcinoma metastático do pâncreas, em combinação com 5 fluorouracilo (5 fu) e leucovorina (lv), em pacientes adultos que progrediram após a terapia baseada em gemcitabina.

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir - infecções por hiv - antivirais para uso sistêmico - 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.

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

vertex pharmaceuticals (ireland) limited - tezacaftor, ivacaftor - fibrose cística - outros produtos do sistema respiratório - symkevi is indicated in a combination regimen with ivacaftor tablets for the treatment of patients with cystic fibrosis (cf) aged 6 years and older who are homozygous for the f508del mutation or who are heterozygous for the f508del mutation and have one of the following mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene: p67l, r117c, l206w, r352q, a455e, d579g, 711+3a→g, s945l, s977f, r1070w, d1152h, 2789+5g→a, 3272 26a→g, and 3849+10kbc→t.

Brazīlija - portugāļu - ANVISA (Agência Nacional de Vigilância Sanitária)

boehringer ingelheim do brasil quÍmica e farmacÊutica ltda. - dimaleato de afatinibe - antineoplasico