DASATINIB PHAROS 50 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dasatinib pharos 50 mg

remedica ltd. - cipru - dasatinibum - compr. film. - 50mg - inhibitori de protein-kinaza

DASATINIB PHAROS 70 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dasatinib pharos 70 mg

remedica ltd. - cipru - dasatinibum - compr. film. - 70mg - inhibitori de protein-kinaza

DASATINIB SANDOZ 100 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dasatinib sandoz 100 mg

remedica ltd. - cipru - dasatinibum - compr. film. - 100mg - inhibitori de protein-kinaza

DASATINIB SANDOZ 20 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dasatinib sandoz 20 mg

remedica ltd. - cipru - dasatinibum - compr. film. - 20mg - inhibitori de protein-kinaza

DASATINIB SANDOZ 50 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dasatinib sandoz 50 mg

remedica ltd. - cipru - dasatinibum - compr. film. - 50mg - inhibitori de protein-kinaza

DASATINIB SANDOZ 70 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dasatinib sandoz 70 mg

remedica ltd. - cipru - dasatinibum - compr. film. - 70mg - inhibitori de protein-kinaza

Jayempi Uniunea Europeană - română - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - respingerea grefei - imunosupresoare - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

Vokanamet Uniunea Europeană - română - EMA (European Medicines Agency)

vokanamet

janssen-cilag international nv - canagliflozin, clorhidrat de metformină - diabetul zaharat, tip 2 - medicamente utilizate în diabet - vokanamet este indicat la adulți cu vârsta de 18 ani și peste cu diabet zaharat de tip 2 ca adjuvant la dietă și exercițiu fizic pentru îmbunătățirea controlului glicemic:la pacienții care nu sunt controlate în mod adecvat asupra lor cu dozele maxime tolerate de metformină singur pacienții lor cu dozele maxime tolerate de metformină împreună cu alte medicamente de scădere a glicemiei, inclusiv insulina, atunci când acestea nu se realizează un control glicemic adecvat. la pacienții deja tratați cu combinația de canagliflozin și metformin separat tabletsfor rezultatele studiului cu privire la o combinație de terapii, efecte asupra controlului glicemic și evenimente cardiovasculare, iar populațiile studiate, a se vedea secțiunile 4. 4, 4. 5 și 5.