Italia - italiano - Ministero della Salute

allergan industrie sas - prodotti riassorbibili per riempimento e ricostruzione

Italia - italiano - Ministero della Salute

allergan industrie sas - prodotti riassorbibili per riempimento e ricostruzione

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - pazopanib - carcinoma, cellule renali - agenti antineoplastici - carcinoma a cellule renali (rcc)votrient è indicato negli adulti per il trattamento di prima linea avanzate di carcinoma a cellule renali (rcc) e per i pazienti che hanno ricevuto una precedente terapia con citochine per malattia avanzata. il sarcoma dei tessuti molli (sts)votrient è indicato per il trattamento di pazienti adulti con selettiva sottotipi di avanzata sarcoma dei tessuti molli (sts) che hanno ricevuto una precedente chemioterapia per la malattia metastatica o che hanno progredito entro 12 mesi dopo (neo)adiuvante terapia. l'efficacia e la sicurezza sono stati stabiliti soltanto in alcuni sts istologico del tumore sottotipi.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

verfora sa - chlorhexidini digluconas, lidocaini hydrochloridum monohydricum - soluzione - chlorhexidini digluconas 180 µg ut chlorhexidini digluconatis solutio, lidocaini hydrochloridum monohydricum 45 µg, acidum citricum monohydricum, glycerolum, saccharinum natricum, levomentholum, cineolum, ethanolum 96 per centum, aqua purificata, ad solutionem pro dosi corresp. ethanolum 44.4 % v/v, doses pro vase 333. - i sintomi nei casi di infiammazione della gola - synthetika

Italia - italiano - Ministero della Salute

ecuphar veterinaria slu - lidocaina cloridrato - lidocaina cloridrato - 200 milligrammo (i), lidocaina cloridrato - 20 mg, lidocaina cloridrato - 200 mg - lidocaine

Italia - italiano - Ministero della Salute

zoetis italia s.r.l. - lidocaina cloridrato - lidocaina cloridrato - 2 grammo (i), lidocaina cloridrato - 2 g - lidocaine

Italia - italiano - Ministero della Salute

dechra regulatory b.v. - lidocaina cloridrato - lidocaina cloridrato - 20 mg - lidocaine

Italia - italiano - Ministero della Salute

richter pharma ag - lidocaina cloridrato - lidocaina cloridrato - nd, lidocaina cloridrato - 24.65 mg/ml - lidocaine

Unione Europea - italiano - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - agenti antineoplastici - abecma is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Unione Europea - italiano - EMA (European Medicines Agency)

fresenius kabi deutschland gmbh - tocilizumab - arthritis, rheumatoid; cytokine release syndrome; arthritis, juvenile rheumatoid; covid-19 virus infection; giant cell arteritis - immunosoppressori - 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.