DOZZEX 30 mg Rumänien - Rumänisch - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

dozzex 30 mg

pharmascience international ltd. - cipru - duloxetinum - caps. gastrorez. - 30mg - antidepresive alte antidepresive

DOZZEX 60 mg Rumänien - Rumänisch - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

dozzex 60 mg

pharmascience international ltd. - cipru - duloxetinum - caps. gastrorez. - 60mg - antidepresive alte antidepresive

SERTRALINA ACCORD 100 mg Rumänien - Rumänisch - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

sertralina accord 100 mg

accord healthcare limited - marea britanie - sertralinum - compr. film. - 100mg - antidepresive inhibitori selectivi ai recaptarii serotoninei

SERTRALINA ACCORD 50 mg Rumänien - Rumänisch - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

sertralina accord 50 mg

accord healthcare limited - marea britanie - sertralinum - compr. film. - 50mg - antidepresive inhibitori selectivi ai recaptarii serotoninei

Dupixent Europäische Union - Rumänisch - EMA (European Medicines Agency)

dupixent

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agenți pentru dermatită, cu excepția corticosteroizilor - 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.

Lacosamide Accord Europäische Union - Rumänisch - EMA (European Medicines Agency)

lacosamide accord

accord healthcare s.l.u. - lacosamid - epilepsie - antiepileptice, - 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.

Crysvita Europäische Union - Rumänisch - EMA (European Medicines Agency)

crysvita

kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - medicamente pentru tratamentul bolilor osoase - crysvita is indicated for the treatment of x-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. crysvita is indicated for the treatment of fgf23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.

ABACAVIR/LAMIVUDINA VALE 600 mg/300 mg Rumänien - Rumänisch - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

abacavir/lamivudina vale 600 mg/300 mg

mcdermott laboratories limited t/a - irlanda - abacavirum+lamivudinum - compr. film. - 600mg/300mg - antivirale cu actiune directa antivirale pentru tratamentul infectiei cu hiv, combinatii

ABACAVIR/LAMIVUDINA ZENTIVA 600 mg/300 mg Rumänien - Rumänisch - ANMDM (Agenția Națională a Medicamentului și a Dispozitivelor Medicale din România)

abacavir/lamivudina zentiva 600 mg/300 mg

zentiva, k.s. - republica ceha - abacavirum+lamivudinum - compr. film. - 600mg/300mg - antivirale cu actiune directa antivirale pentru tratamentul infectiei cu hiv, combinatii