Europeiska unionen - portugisiska - EMA (European Medicines Agency)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vacinas - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Brasilien - portugisiska - ANVISA (Agência Nacional de Vigilância Sanitária)

laboratÓrio teuto brasileiro s/a - carbocisteÍna - expectorantes balsamicos e mucolitico

Europeiska unionen - portugisiska - EMA (European Medicines Agency)

laboratorios farmacéuticos rovi, s.a. - risperidone - esquizofrenia - psicolepticos - treatment of schizophrenia in adults for whom tolerability and effectiveness has been established with oral risperidone.

Europeiska unionen - portugisiska - EMA (European Medicines Agency)

pharmaswiss ceska republika s.r.o - pegaptanib - degeneração macular úmida - oftalmológicos - macugen é indicado para o tratamento da degeneração macular neovascular (úmida) relacionada à idade (amd).

Europeiska unionen - portugisiska - EMA (European Medicines Agency)

novartis europharm limited  - brolucizumab - degeneração macular úmida - oftalmológicos - beovu é indicado em adultos para o tratamento de neovascular (úmida) degeneração macular relacionada à idade (amd).

Europeiska unionen - portugisiska - EMA (European Medicines Agency)

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vacinas - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. o uso desta vacina deve ser de acordo com as recomendações oficiais.

Europeiska unionen - portugisiska - EMA (European Medicines Agency)

n.v. organon - ganirelix - reproductive techniques, assisted; ovulation induction; infertility, female - hormonas e análises pituitárias e hipotalâmicas - a prevenção de surtos prematuros de luteinização-hormônio em mulheres submetidas à hiperestimulação ovárica controlada para técnicas de reprodução assistida. em estudos clínicos, o orgalutran foi usado com recombinante humano hormônio folículo-estimulante ou corifollitropin alfa, sustentado folículo estimulante.

Europeiska unionen - portugisiska - EMA (European Medicines Agency)

chemical works of gedeon richter plc. (gedeon richter plc.) - ganirelix acetate - reproductive techniques, assisted; ovulation induction; infertility, female - hormonas e análises pituitárias e hipotalâmicas - prevention of premature luteinising hormone (lh) surges in women undergoing controlled ovarian hyperstimulation (coh) for assisted reproduction techniques (art).

Portugal - portugisiska - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

laboratórios effik, sociedade unipessoal, lda. - progesterona - cápsula mole - 100 mg - progesterona 100 mg - progesterone - genérico - duração do tratamento: longa duração

Portugal - portugisiska - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

theramex ireland limited - ganirrelix - solução injetável em seringa pré-cheia - 0.25 mg/0.5 ml - ganirrelix 0.25 mg - ganirelix - genérico - duração do tratamento: curta ou média duração