Бразилия - португалски - ANVISA (Agência Nacional de Vigilância Sanitária)

upjohn brasil importadora e distribuidora de medicamentos ltda. - pregabalina - anticonvulsivantes

Бразилия - португалски - ANVISA (Agência Nacional de Vigilância Sanitária)

aché laboratórios farmacêuticos s.a - pregabalina - anticonvulsivantes

Португалия - португалски - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

aristo pharma gmbh - levofloxacina - comprimido revestido por película - 250 mg - levofloxacina hemi-hidratada 256.23 mg - levofloxacin - genérico - duração do tratamento: curta ou média duração

Португалия - португалски - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

generis farmacêutica, s.a. - levofloxacina - comprimido revestido por película - 250 mg - levofloxacina hemi-hidratada 256.23 mg - levofloxacin - genérico - duração do tratamento: curta ou média duração

Португалия - португалски - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

aristo pharma gmbh - levofloxacina - comprimido revestido por película - 500 mg - levofloxacina hemi-hidratada 512.46 mg - levofloxacin - genérico - duração do tratamento: curta ou média duração

Португалия - португалски - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

aristo pharma gmbh - levofloxacina - comprimido revestido por película - 250 mg - levofloxacina hemi-hidratada 256.23 mg - levofloxacin - genérico - duração do tratamento: curta ou média duração

Бразилия - португалски - ANVISA (Agência Nacional de Vigilância Sanitária)

eurofarma laboratÓrios s.a. - pregabalina - anticonvulsivantes

Европейски съюз - португалски - EMA (European Medicines Agency)

fresenius kabi deutschland gmbh - tocilizumab - arthritis, rheumatoid; cytokine release syndrome; arthritis, juvenile rheumatoid; covid-19 virus infection; giant cell arteritis - imunossupressores - tyenne, in combination with methotrexate (mtx), is indicated for- the treatment of severe, active and progressive rheumatoid arthritis (ra) in adults not previously treated with mtx. - the treatment of moderate to severe active ra in adult patients who have either responded inadequately to, or who were intolerant to, previous therapy with one or more disease-modifying anti-rheumatic drugs (dmards) or tumour necrosis factor (tnf) antagonists. in these patients, tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tocilizumab has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function when given in combination with methotrexate. tyenne is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation. tyenne is indicated for the treatment of active systemic juvenile idiopathic arthritis (sjia) in patients 1 year of age and older, who have responded inadequately to previous therapy with nsaids and systemic corticosteroids. tyenne can be given as monotherapy (in case of intolerance to mtx or where treatment with mtx is inappropriate) or in combination with mtx. tyenne in combination with methotrexate (mtx) is indicated for the treatment of juvenile idiopathic polyarthritis (pjia; rheumatoid factor positive or negative and extended oligoarthritis) in patients 2 years of age and older, who have responded inadequately to previous therapy with mtx. tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tyenne is indicated for the treatment of chimeric antigen receptor (car) t cell-induced severe or life-threatening cytokine release syndrome (crs) in adults and paediatric patients 2 years of age and older. tyenne is indicated for the treatment of giant cell arteritis (gca) in adult patients.

Европейски съюз - португалски - EMA (European Medicines Agency)

actavis group ptc ehf   - cloridrato de pioglitazona - diabetes mellitus, tipo 2 - drogas usadas em diabetes - pioglitazone is indicated as second or third line treatment of type 2 diabetes mellitus as described below:as monotherapyin adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance. as dual oral therapy in combination withmetformin, in adult patients (particularly overweight patients) with insufficient glycaemic control despite maximal tolerated dose of monotherapy with metformin. a sulphonylurea, only in adult patients who show intolerance to metformin or for whom metformin is contraindicated, with insufficient glycaemic control despite maximal tolerated dose of monotherapy with a sulphonylurea. as triple oral therapy in combination withmetformin and a sulphonylurea, in adult patients (particularly overweight patients) with insufficient glycaemic control despite dual oral therapy. pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance (see section 4. após o início da terapia com pioglitazona, os pacientes devem ser examinados após 3 a 6 meses para avaliar a adequação da resposta ao tratamento (e. redução na hba1c). em pacientes que não conseguem mostrar uma resposta adequada, a pioglitazona deve ser descontinuado. na luz dos riscos potenciais com terapia prolongada, o médico prescritor deve confirmar subsequentes rotina comentários de que o benefício de pioglitazona é mantida (ver secção 4.

Европейски съюз - португалски - EMA (European Medicines Agency)

pfizer europe ma eeig - tofacitinib - artrite, reumatóide - imunossupressores - rheumatoid arthritistofacitinib in combination with methotrexate (mtx) is indicated for the treatment of moderate to severe active rheumatoid arthritis (ra) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (dmards) (see section 5. tofacitinib can be given as monotherapy in case of intolerance to mtx or when treatment with mtx is inappropriate (see sections 4. 4 e 4. psoriatic arthritistofacitinib in combination with mtx is indicated for the treatment of active psoriatic arthritis (psa) in adult patients who have had an inadequate response or who have been intolerant to a prior disease modifying antirheumatic drug (dmard) therapy (see section 5. ulcerative colitistofacitinib is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent (see section 5. tofacitinib is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (rheumatoid factor positive [rf+] or negative [rf-] polyarthritis and extended oligoarthritis), and juvenile psoriatic arthritis (psa) in patients 2 years of age and older, who have responded inadequately to previous therapy with disease modifying antirheumatic drugs (dmards). tofacitinib can be given in combination with methotrexate (mtx) or as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. ankylosing spondylitistofacitinib is indicated for the treatment of adult patients with active ankylosing spondylitis (as) who have responded inadequately to conventional therapy.