Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

alfa intes industria terapeutica splendore s.r.l. - corticosteroidi e antiinfettivi in associazione - corticosteroidi e antiinfettivi in associazione

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

recordati industria chimica e farmaceutica s.p.a. - corticosteroidi - corticosteroidi

Italia - italiano - Ministero della Salute

msd animal health s.r.l. - clotrimazolo, betametasone, gentamicina - clotrimazolo - 8.8 mg/ml; betametasone - 0.88 mg/ml; gentamicina - 2640 unit? internazionali, clotrimazolo - 8.8 mg/ml; betametasone - 0.88 mg/ml; gentamicina - 2640 unit? internazionali, clotrimazolo - 8.8 mg/ml; betametasone - 0.88 mg/ml; gentamicina - 2640 unit? internazionali, betametasone - 0.88 mg/ml; gentamicina - 2640 unit? internazionali; clotrimazolo - 8.8 mg/ml, clotrimazolo - 8.8 mg/ml; gentamicina - 2640 unit? internazionali; betametasone - 0.88 mg/ml, clotrimazolo - 8.8 mg/ml; betametasone - 0.88 mg/ml; gentamicina - 2640 ui, betametasone - 0.88 mg/ml; clotrimazolo - 8.8 mg/ml; gentamicina - 2640 ui, betametasone - 0.88 mg/ml; gentamicina - 2640 ui; clotrimazolo - 8.8 mg/ml, clotrimazolo - 8.8 mg/ml; gentamicina - 2640 ui; betametasone - 0.88 mg/ml, gentamicina - 2640 ui; clotrimazolo - 8.8 mg/ml; betametasone - 0.88 mg/ml - corticosteroids and antiinfectives in combination

Italia - italiano - Ministero della Salute

boehringer ingelheim animal health italia s.p.a - tiabendazolo, desametasone, neomicina solfato - tiabendazolo - 4 grammo (i) ; desametasone - 1 grammo (i) ; neomicina solfato - 0.32 grammo (i), desametasone - 1 g; tiabendazolo - 4 g; neomicina solfato - 0.32 g - corticosteroids, moderately potent, combinations with antibiotics

Italia - italiano - Ministero della Salute

alpha-vet veterinary ltd - ketoconazolo, prednisolone, marboflossacina - ketoconazolo - 2.04 mg; prednisolone - 0.93 mg; marboflossacina - 1.03 mg/ml, marboflossacina - 1.03 mg/ml; prednisolone - 0.93 mg; ketoconazolo - 2.04 mg - corticosteroids, other combinations

Italia - italiano - Ministero della Salute

acme s.r.l. - stanozololo - stanozololo - 1.5 mg - stanozolol

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agenti per dermatiti, esclusi i corticosteroidi - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Unione Europea - italiano - EMA (European Medicines Agency)

samsung bioepis nl b.v. - adalimumab - spondylitis, ankylosing; arthritis, rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; hidradenitis suppurativa; arthritis - immunosoppressori - reumatoide arthritisimraldi in combinazione con metotressato è indicato per:il trattamento di moderata a grave artrite reumatoide attiva in pazienti adulti quando la risposta ai modificanti la malattia farmaci anti-reumatici, incluso il metotressato è stata inadeguata. il trattamento di grave, attiva e progressiva artrite reumatoide negli adulti non precedentemente trattati con metotressato. imraldi può essere somministrato come monoterapia in caso di intolleranza al metotressato o quando il trattamento continuato con metotressato è inappropriato. adalimumab ha dimostrato di ridurre il tasso di progressione del danno articolare misurato da x-ray e di migliorare la funzione fisica, quando somministrato in combinazione con metotressato. juvenile idiopathic arthritispolyarticular juvenile idiopathic arthritisimraldi 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). imraldi can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate (for the efficacy in monotherapy see section 5. adalimumab non è stato studiato in pazienti di età inferiore a 2 anni. enthesitis-related arthritisimraldi 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 (see section 5. axial spondyloarthritisankylosing spondylitis (as)imraldi 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 asimraldi 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 non-steroidal anti-inflammatory drugs (nsaids). psoriasica arthritisimraldi è indicato per il trattamento di attiva e progressiva artrite psoriasica negli adulti, quando la risposta alla precedente la malattia (disease modifying anti-rheumatic drug therapy è stata inadeguata. adalimumab has been shown to reduce the rate of progression of peripheral joint damage as measured by x-ray in patients with polyarticular symmetrical subtypes of the disease (see section 5. 1) e di migliorare la funzione fisica. psoriasisimraldi è indicato per il trattamento di moderata a grave psoriasi a placche cronica in pazienti adulti che non sono candidati per la terapia sistemica. pediatrica placca psoriasisimraldi è indicato per il trattamento di una grave psoriasi a placche cronica nei bambini e negli adolescenti a partire dai 4 anni di età che hanno avuto una risposta inadeguata o sono inadeguati, i candidati per la terapia attuale e phototherapies. hidradenitis suppurativa (hs)imraldi 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 (see sections 5. 1 e 5. il morbo di crohn diseaseimraldi è indicato per il trattamento di moderata a grave malattia di crohn attiva grave, in pazienti adulti che non abbiano risposto nonostante un completo e adeguato corso di terapia con corticosteroidi e/o immunosoppressori; o che sono intolleranti o hanno controindicazioni mediche per tali terapie. paediatric crohn's diseaseimraldi 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 haveulcerative colitisimraldi 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 mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. paediatric ulcerative colitisimraldi 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. uveitisimraldi 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 corticosteroidsparing, or in whomcorticosteroid treatment is inappropriate. paediatric uveitisimraldi 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.

Unione Europea - italiano - EMA (European Medicines Agency)

nova laboratories ireland limited - azathioprine - reiezione del trapianto - immunosoppressori - 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.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

laboratorio chimico farmaceutico a. sella s.r.l. - sodio fosfato - sodio fosfato