Lietuva - lietuviešu - SMCA (Valstybinė vaistų kontrolės tarnyba)

mcneil healthcare (ireland) limited - pseudoefedrino hidrochloridas/triprolidino hidrochloridas - tabletės - 30 mg/1,25 mg/5 ml; 60 mg/2,5 mg - pseudoephedrine, combinations

Lietuva - lietuviešu - SMCA (Valstybinė vaistų kontrolės tarnyba)

ucb pharma oy finland - cetirizino dihidrochloridas/pseudoefedrino hidrochloridas - pailginto atpalaidavimo tabletės - 5 mg/120 mg - pseudoephedrine, combinations

Lietuva - lietuviešu - SMCA (Valstybinė vaistų kontrolės tarnyba)

laboratoire innotech international - neomicino sulfatas/polimiksino b sulfatas/nistatinas - makšties minkštosios kapsulės - 35000 tv/35000 tv/100000 tv - nystatin, combinations

Lietuva - lietuviešu - SMCA (Valstybinė vaistų kontrolės tarnyba)

teva b.v. - imipenemas/cilastatinas - milteliai infuziniam tirpalui - 500 mg/500 mg - imipenem and cilastatin

Lietuva - lietuviešu - SMCA (Valstybinė vaistų kontrolės tarnyba)

panpharma - kanamicinas - milteliai injekciniam tirpalui - 1 g - kanamycin

Lietuva - lietuviešu - SMCA (Valstybinė vaistų kontrolės tarnyba)

glaxosmithkline consumer healthcare (uk) trading limited - paracetamolis/pseudoefedrinas - sirupas - 500 mg/30 mg/30 ml - other cold preparations ;paracetamol, combinations excl. psycholeptics

Eiropas Savienība - lietuviešu - EMA (European Medicines Agency)

sandoz gmbh - adalimumabas - arthritis, rheumatoid; arthritis, psoriatic; spondylitis, ankylosing; uveitis; hidradenitis suppurativa; colitis, ulcerative; arthritis, juvenile rheumatoid; crohn disease; skin diseases, papulosquamous - imunosupresantai - rheumatoid arthritishyrimoz in combination with methotrexate, is indicated for:- the treatment of moderate to severe, active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drugs including methotrexate has been inadequate. - the treatment of severe, active and progressive rheumatoid arthritis in adults not previously treated with methotrexate. hyrimoz gali būti suteikiamas kaip monotherapy atveju netolerancija, kad metotreksato ar kai tolesnis gydymas metotreksatu netinka. adalimumabas buvo įrodyta, kad sumažinti greitį progresavimą, bendrą žalą, vertinant pagal x-ray ir gerinti fizinę funkciją, skiriant kartu su metotreksatu. juvenile idiopathic arthritis- polyarticular juvenile idiopathic arthritishyrimoz in combination with methotrexate is indicated for the treatment of active polyarticular juvenile idiopathic arthritis, in patients from the age of 2 years who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (dmards). hyrimoz gali būti suteikiamas kaip monotherapy atveju netolerancija, kad metotreksato ar kai tolesnis gydymas metotreksatu netinka. adalimumabas nebuvo tirtas pacientams, jaunesniems negu 2 metų. - enthesitis-related arthritishyrimoz is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy. axial spondyloarthritis- ankylosing spondylitis (as)hyrimoz is indicated for the treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. - axial spondyloarthritis without radiographic evidence of ashyrimoz is indicated for the treatment of adults with severe axial spondyloarthritis without radiographic evidence of as but with objective signs of inflammation by elevated crp and / or mri, who have had an inadequate response to, or are intolerant to nonsteroidal anti-inflammatory drugs. psoriatic arthritishyrimoz is indicated for the treatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate. adalimumabas buvo įrodyta, kad sumažinti greitį progresavimą, periferinių sąnarių pažeidimai, kaip matuojamas x-ray sergant poliartritu simetriškus potipius ligą ir pagerinti fizinį funkcija. psoriasishyrimoz is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy. paediatric plaque psoriasishyrimoz is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapies. hidradenitis suppurativa (hs)hyrimoz is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adults and adolescents from 12 years of age with an inadequate response to conventional systemic hs therapy. crohn’s diseasehyrimoz is indicated for treatment of moderately to severely active crohn’s disease in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and / or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies. paediatric crohn's diseasehyrimoz is indicated for the treatment of moderately to severely active crohn's disease in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy and a corticosteroid and / or an immunomodulator, or who are intolerant to or have contraindications for such therapies.  paediatric ulcerative colitishyrimoz is indicated for the treatment of moderately to severely active ulcerative colitis in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including corticosteroids and/or 6-mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. ulcerative colitishyrimoz is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. uveitishyrimoz is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroid-sparing, or in whom corticosteroid treatment is inappropriate. paediatric uveitishyrimoz is indicated for the treatment of paediatric chronic non-infectious anterior uveitis in patients from 2 years of age who have had an inadequate response to or are intolerant to conventional therapy, or in whom conventional therapy is inappropriate.

Eiropas Savienība - lietuviešu - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinurija, paroksizminis - selektyvūs imunosupresantai - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.

Lietuva - lietuviešu - SMCA (Valstybinė vaistų kontrolės tarnyba)

interhygiene gmbh, neufelder straβe 30, d-27472 cuxhaven, vokietija - vandenilio peroksidas; vandenilio peroksidas; vandenilio peroksidas - veikliosios medžiagos cas nr.: 7722-84-1, eb nr.: 231-765-0, veikliosios medžiagos pavadinimas: vandenilio peroksidas, koncentracija: 25% , veiklioji; veikliosios medžiagos cas nr.: 7722-84-1, eb nr.: 231-765-0, veikliosios medžiagos pavadinimas: vandenilio peroksidas, koncentracija: 25% , veiklioji; veikliosios medžiagos cas nr.: 7722-84-1, eb nr.: 231-765-0, veikliosios medžiagos pavadinimas: vandenilio peroksidas, koncentracija: 25% , veiklioji - veterinarinė higiena

Lietuva - lietuviešu - SMCA (Valstybinė vaistų kontrolės tarnyba)

us pharmacia sp. z o.o. - paracetamolis/pseudoefedrino hidrochloridas/dekstrometorfano hidrobromidas/chlorfenamino maleatas - plėvele dengtos tabletės - 500 mg/30 mg/15 mg/2 mg - paracetamol, combinations excl. psycholeptics