Európai Unió - portugál - EMA (European Medicines Agency)

sanofi pasteur europe - filamentous haemagglutinin, haemophilus influenzae type b polysaccharide (polyribosylribitol phosphate), hepatitis b surface antigen, pertussis toxoid, poliovirus (inactivated) type 1 (mahoney strain) produced on vero cells, poliovirus (inactivated) type 2 (mef-1 strain) produced on vero cells, poliovirus (inactivated) type 3 (saukett strain) produced on vero cells, tetanus protein, tetanus toxoid adsorbed on aluminium hydroxide, hydrated, diphtheria toxoid - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; poliomyelitis; diphtheria - vacinas - o hexyon (dtap-ipv-hb-hib) é indicado para a vacinação primária e de reforço de bebês e crianças de seis semanas contra a difteria, o tétano, a tosse convulsa, a hepatite b, a poliomielite e as doenças invasivas causadas por haemophilus influenzae tipo b (hib). o uso desta vacina deve ser de acordo com as recomendações oficiais.

Európai Unió - portugál - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - adalimumab - spondylitis, ankylosing; arthritis, juvenile rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; arthritis, rheumatoid - imunossupressores - consulte o documento de informações do produto.

Európai Unió - portugál - EMA (European Medicines Agency)

ceva santé animale - benazepril hydrochloride, spironolactone - sistema cardiovascular - cães - para o tratamento da insuficiência cardíaca congestiva causada por doença valvular degenerativa crônica em cães (com suporte diurético conforme apropriado).

Európai Unió - portugál - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - diphtheria toxoid, tetanus toxoid, bordetella pertussis antigens (pertussis toxoid, filamentous haemagglutinin, pertactin), poliovirus (inactivated) (type 1 (mahoney strain), type 2 (mef-1 strain), type 3 (saukett strain)), hepatitis b surface antigen - hepatitis b; tetanus; immunization; whooping cough; poliomyelitis; diphtheria - vacinas - infanrix penta é indicado para a vacinação primária e de reforço de bebês contra a difteria, tétano, tosse convulsa, hepatite b e poliomielite.

Európai Unió - portugál - EMA (European Medicines Agency)

virbac s.a. - aceponato de hidrocortisona - corticosteróides, preparações dermatológicas - cães - para tratamento sintomático de dermatoses inflamatórias e pruriginosas em cães. for alleviation of clinical signs associated with atopic dermatitis in dogs.

Európai Unió - portugál - EMA (European Medicines Agency)

vetoquinol s.a. - emodepside, toltrazuril - produtos antiparasitário, inseticidas e repelentes - cães - para os cães, quando misturado infecções parasitárias causadas por nematelmintos e coccidia das seguintes espécies de suspeita ou comprovada:as lombrigas (nematóides)toxocara canis (adultos maduros, imaturos adultos, l4);uncinaria stenocephala (adulto maduro);ancylostoma caninum (adulto maduro). coccidiaisospora ohioensis complexo;isospora canis. procox é eficaz contra a replicação de isospora e também contra o derramamento de oocistos. embora o tratamento reduza a propagação da infecção, não será eficaz contra os sinais clínicos de infecção em animais já infectados.

Európai Unió - portugál - EMA (European Medicines Agency)

ceva santé animale - espironolactona - diuréticos - cães - para uso em combinação com terapia padrão (incluindo suporte diurético, quando necessário) para o tratamento de insuficiência cardíaca congestiva causada por insuficiência valvar em cães.

Európai Unió - portugál - EMA (European Medicines Agency)

eli lilly and company limited - spinosad, milbemycin oxime - antiparasitários produtos, insecticidas e repelentes, endectocides - cães - para o tratamento e prevenção de pulgas (ctenocephalides felis) a infestação em cães onde um ou mais dos seguintes indicações são necessários simultaneamente: prevenção da doença de dirofilariose (l3, l4 dirofilaria immitis);prevenção de angiostrongylosis reduzindo o nível de infecção com imaturo adultos (l5) angiostrongylus vasorum;tratamento do aparelho digestivo nematóide de infecções causadas por ancilóstomo (l4, imatura e adulta, l5) e adulto ancylostoma caninum), lombrigas (imaturos adultos l5 e adultos toxocara canis e adultos toxascaris leonina)) e whipworm (adulto trichuris vulpis).

Európai Unió - portugál - EMA (European Medicines Agency)

merck sharp & dohme b.v. - pembrolizumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; endometrial neoplasms - agentes antineoplásicos - melanomakeytruda as monotherapy is indicated for the treatment of adults and adolescents aged 12 years and older with advanced (unresectable or metastatic) melanoma. keytruda as monotherapy is indicated for the adjuvant treatment of adults and adolescents aged 12 years and older with stage iib, iic, or with stage iii melanoma and lymph node involvement who have undergone complete resection. non small cell lung carcinoma (nsclc)keytruda as monotherapy is indicated for the adjuvant treatment of adults with non-small cell lung carcinoma who are at high risk of recurrence following complete resection and platinum based chemotherapy (for selection criteria, see section 5. keytruda as monotherapy is indicated for the first line treatment of metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 50% tumour proportion score (tps) with no egfr or alk positive tumour mutations. keytruda, in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of metastatic non squamous non small cell lung carcinoma in adults whose tumours have no egfr or alk positive mutations. keytruda, in combination with carboplatin and either paclitaxel or nab paclitaxel, is indicated for the first line treatment of metastatic squamous non small cell lung carcinoma in adults. keytruda  as monotherapy is indicated for the treatment of locally advanced or metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 1% tps and who have received at least one prior chemotherapy regimen. pacientes com egfr ou alk positivo tumor mutações também deve ter recebido a terapia direcionada antes de receber keytruda. classical hodgkin lymphoma (chl)keytruda as monotherapy is indicated for the treatment of adult and paediatric patients aged 3 years and older with relapsed or refractory classical hodgkin lymphoma who have failed autologous stem cell transplant (asct) or following at least two prior therapies when asct is not a treatment option. urothelial carcinomakeytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who have received prior platinum containing chemotherapy. keytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who are not eligible for cisplatin containing chemotherapy and whose tumours express pd l1 with a combined positive score (cps) ≥ 10. head and neck squamous cell carcinoma (hnscc)keytruda, as monotherapy or in combination with platinum and 5 fluorouracil (5 fu) chemotherapy, is indicated for the first line treatment of metastatic or unresectable recurrent head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a cps ≥ 1. keytruda as monotherapy is indicated for the treatment of recurrent or metastatic head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a ≥ 50% tps and progressing on or after platinum containing chemotherapy. renal cell carcinoma (rcc)keytruda, in combination with axitinib, is indicated for the first line treatment of advanced renal cell carcinoma in adults. keytruda  as monotherapy is indicated for the adjuvant treatment of adults with renal cell carcinoma at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions (for selection criteria, please see section 5. microsatellite instability high (msi-h) or mismatch repair deficient (dmmr) cancerscolorectal cancer (crc)keytruda as monotherapy is indicated for theadults with msi-h or dmmr colorectal cancer in the following settings:first line treatment of metastatic microsatellite instability high (msi h) or mismatch repair deficient (dmmr) colorectal cancer in adults;treatment of unresectable or metastatic colorectal cancer after previous fluoropyrimidine based combination therapy.  non-colorectal cancerskeytruda as monotherapy is indicated for the treatment of the following msi h or dmmr tumours in adults with:advanced or recurrent endometrial carcinoma, who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation;unresectable or metastatic gastric, small intestine, or biliary cancer, who have disease progression on or following at least one prior therapy. oesophageal carcinomakeytruda, in combination with platinum and fluoropyrimidine based chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic carcinoma of the oesophagus or her-2 negative gastroesophageal junction adenocarcinoma, in adults whose tumours express pd l1 with a cps ≥ 10. triple negative breast cancer (tnbc)keytruda, in combination with chemotherapy as neoadjuvant treatment, and then continued as monotherapy as adjuvant treatment after surgery, is indicated for the treatment of adults with locally advanced, or early stage triple negative breast cancer at high risk of recurrence. keytruda, in combination with chemotherapy, is indicated for the treatment of locally recurrent unresectable or metastatic triple negative breast cancer in adults whose tumours express pd l1 with a cps ≥ 10 and who have not received prior chemotherapy for metastatic disease. endometrial carcinoma (ec)keytruda, in combination with lenvatinib, is indicated for the treatment of advanced or recurrent endometrial carcinoma in adults who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation. cervical cancerkeytruda, in combination with chemotherapy with or without bevacizumab, is indicated for the treatment of persistent, recurrent, or metastatic cervical cancer in adults whose tumours express pd l1 with a cps ≥ 1. gastric or gastro-oesophageal junction (gej) adenocarcinomakeytruda, in combination with trastuzumab, fluoropyrimidine and platinum-containing chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic her2-positive gastric or gastro-oesophageal junction adenocarcinoma in adults whose tumours express pd-l1 with a cps ≥ 1.

Európai Unió - portugál - EMA (European Medicines Agency)

sanofi belgium - alemtuzumab - esclerose múltipla - imunossupressores seletivos - lemtrada é indicado para pacientes adultos com esclerose múltipla remitente-remitente (rcms) com doença ativa definida por características clínicas ou de imagem.