Celvapan União Europeia - português - EMA (European Medicines Agency)

celvapan

nanotherapeutics bohumil, s.r.o. - whole virion influenza vaccine, inactivated containing antigen of strain a/california/07/2009 (h1n1)v - disease outbreaks; influenza, human; immunization - vacinas - profilaxia da gripe causada pelo vírus a (h1n1) v 2009. celvapan deve ser usado de acordo com orientação oficial.

OENOTHERA BIENNIS Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

oenothera biennis

zenimport comercio importacao e exportacao ltda - fitoterapico simples

Ellura 195.7 - 216.9 mg Cápsula Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

ellura 195.7 - 216.9 mg cápsula

laboratoire pharmaceutique pharmatoka - n/a - cápsula - 195.7 - 216.9 mg - extrato seco e refinado do sumo do fruto de vaccinium macrocarpon aiton, der 250:1, solvente: etanol 70% (v/v) 195.7 mg - other urologicals - tradicional à base de plantas - duração do tratamento: curta ou média duração

Ellura 195.7 - 216.9 mg Cápsula Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

ellura 195.7 - 216.9 mg cápsula

laboratoire pharmaceutique pharmatoka - n/a - cápsula - 195.7 - 216.9 mg - extrato seco e refinado do sumo do fruto de vaccinium macrocarpon aiton, der 250:1, solvente: etanol 70% (v/v) 195.7 mg - other urologicals - tradicional à base de plantas - duração do tratamento: curta ou média duração

Ellura 195.7 - 216.9 mg Cápsula Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

ellura 195.7 - 216.9 mg cápsula

laboratoire pharmaceutique pharmatoka - n/a - cápsula - 195.7 - 216.9 mg - extrato seco e refinado do sumo do fruto de vaccinium macrocarpon aiton, der 250:1, solvente: etanol 70% (v/v) 195.7 mg - other urologicals - tradicional à base de plantas - duração do tratamento: curta ou média duração

Ellura 195.7 - 216.9 mg Cápsula Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

ellura 195.7 - 216.9 mg cápsula

laboratoire pharmaceutique pharmatoka - n/a - cápsula - 195.7 - 216.9 mg - extrato seco e refinado do sumo do fruto de vaccinium macrocarpon aiton, der 250:1, solvente: etanol 70% (v/v) 195.7 mg - other urologicals - tradicional à base de plantas - duração do tratamento: curta ou média duração

Revolade União Europeia - português - EMA (European Medicines Agency)

revolade

novartis europharm limited - eltrombopag - purpura, trombocitopénica, idiopática - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 e 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 e 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Adakveo União Europeia - português - EMA (European Medicines Agency)

adakveo

novartis europharm limited - crizanlizumab - anemia, célula falciforme - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Oxbryta União Europeia - português - EMA (European Medicines Agency)

oxbryta

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

Broncho-Vaxom Adulto 7 mg Cápsula Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

broncho-vaxom adulto 7 mg cápsula

omedicamed, unipessoal lda - lisados polibacterianos - cápsula - 7 mg - klebsiella ozaenae klebsiella ozaenae ; moraxella (branhammella) catarrhalis moraxella (branhammella) catarrhalis ; staphylococcus aureus staphylococcus aureus ; streptococcus pyogenes streptococcus pyogenes ; klebsiella pneumoniae klebsiella pneumoniae ; streptococcus sanguinis streptococcus sanguinis ; haemophilus influenzae haemophilus influenzae ; streptococcus pneumoniae streptococcus pneumoniae - other respiratory system products - vacina - duração do tratamento: curta ou média duração