Uniunea Europeană - română - EMA (European Medicines Agency)

pfizer europe ma eeig - tofacitinib - artrita, reumatoida - imunosupresoare - 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 și 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.

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

zdorovie srl, companie farmaceutica - clonidinum - comprimate - 0,15 mg

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

farmaco sa, im - natrii chloridum - solutie injectabila - 0,9%

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

bilim pharmaceuticals a.s. - paracetamolum + pseudoephedrinum - pulbere pentru solutie orala - 500 mg + 60 mg

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

zdorovie srl, companie farmaceutica - pancreatinum - comprimate filmate gastrorezistente - 192 mg (5000 ui + 7000 ui + 400 ui)

Uniunea Europeană - română - EMA (European Medicines Agency)

pfizer europe ma eeig  - axitinib - carcinomul, celula renală - protein kinazei - inlyta is indicated for the treatment of adult patients with advanced renal cell carcinoma (rcc) after failure of prior treatment with sunitinib or a cytokine.

România - română - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

timmer antoaneta persoana fizica autorizata -

România - română - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

timmer antoaneta persoana fizica autorizata -

România - română - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

timmer antoaneta persoana fizica autorizata -

România - română - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

timmer antoaneta persoana fizica autorizata -