الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

viatris healthcare limited - imiquimod - keratosis; keratosis, actinic - sýklalyf og krabbameinslyf til dýrafræðilegrar notkunar - zyclara er ætlað fyrir baugi meðferð vísindalega dæmigert, ekki hyperkeratotic, ekki læknafélag, sýnileg eða teljandi geislunarhyrning fullt andlit eða sköllóttur höfði í ónæmiskerfi fullorðnir þegar öðrum baugi meðferð möguleikar eru handa eða minna viðeigandi.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - sitagliptin hydrochloride - sykursýki, tegund 2 - lyf notuð við sykursýki - for adult patients with type 2 diabetes mellitus, sitagliptin accord is indicated to improve glycaemic control:as monotherapy:- in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance. as dual oral therapy in combination with:- metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control. - a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance. - a peroxisome proliferator-activated receptor gamma (ppary) agonist (i. a thiazolidinedione) when use of a ppary agonist is appropriate and when diet and exercise plus the ppary agonist alone do not provide adequate glycaemic control. as triple oral therapy in combination with:- a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. - a ppary agonist and metformin when use of a ppary agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin accord is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - sykursýki, tegund 2 - lyf notuð við sykursýki - for adult patients with type 2 diabetes mellitus:it is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. it is indicated in combination with a sulphonylurea (i. , þrefaldur samsetning meðferð) sem viðbót til að fæði og æfing í sjúklingar ekki nægilega stjórn á eigin hámarks þolað skammt af sjúklingar og sulphonylurea. it is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. it is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - sorafenib tosilate - carcinoma, hepatocellular; carcinoma, renal cell - Æxlishemjandi lyf - hepatocellular carcinomasorafenib accord is indicated for the treatment of hepatocellular carcinoma (see section 5. renal cell carcinomasorafenib accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - teriflunomide - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi, sérhæfður ónæmisbælandi - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - caspofungin asetat - candidiasis; aspergillosis - sveppalyf fyrir almenn nota - meðferð innrásar sveppasýkingu í fullorðinn eða börn sjúklingar. meðferð innrásar aspergillosis í fullorðinn eða börn sjúklingum sem svarar til eða þola amfótericín b, fitu blöndum amfótericín b og/eða ítrakónazól. svara ekki meðferð er skilgreint eins og framgangi sýkingu eða bilun til að bæta eftir að minnsta kosti 7 daga áður en lækninga skammta af árangri mikla meðferð. reynslunni meðferð fyrir ráð sveppasýkingu (eins og candida eða aspergillus) í hita, neutropaenic fullorðinn eða börn sjúklingar.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - síldenafílsítrat - háþrýstingur, lungnabólga - Þvaglát - adultstreatment fullorðinna sjúklinga með lungum háþrýsting flokkast sem hagnýtur ii og iii, til að bæta æfing getu. verkun hefur verið sýnd í frumum lungnaháþrýstingi og lungnaháþrýstingi sem tengist bandvefssjúkdómum. börn populationtreatment af börnum sjúklinga á aldrinum 1 ár til 17 ára gamall með lungum háþrýsting. virkni í varðar endurbætur á æfingu getu eða lungum haemodynamics hefur verið sýnt fram í aðal lungum blóðþrýsting og lungnaháþrýstingi tengslum með meðfæddan hjartasjúkdóm.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - ibandrónsýra - wounds and injuries; breast diseases; neoplastic processes; calcium metabolism disorders; water-electrolyte imbalance - lyf til að meðhöndla beinsjúkdóma - ibandronic sýru er ætlað í fullorðnir forprevention af beinagrind atburðum (sjúkleg beinbrot, bein fylgikvillar þurfa geislameðferð eða skurðaðgerð) í sjúklinga með brjóstakrabbamein og bein meinvörp. meðferð æxli völdum álíka með eða án meinvörp. meðferð beinbrot í tíðahvörf konur á jókst hættan á beinbrot (sjá kafla 5. lækkun í hættu á hryggbrot hefur verið sýnt fram á, virkni á lærlegg háls beinbrot hefur ekki verið staðfest.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - pregabalín - anxiety disorders; epilepsy - antiepileptics, - epilepsypregabalin hvötum er fram eins og venjulega meðferð í fullorðnir með hluta flog með eða án efri almenn ákvörðun er tekin. almenn kvíða disorderpregabalin hvötum er ætlað fyrir meðferð almenn kvíða (himnum) hjá fullorðnum.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

accord healthcare s.l.u. - lacosamíð - flogaveiki - antiepileptics, - lacosamide accord is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. lacosamide accord is indicated as adjunctive therapy•         in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. •         in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.