Europeiska unionen - svenska - EMA (European Medicines Agency)

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - buprenorfin hydroklorid - opioidrelaterade sjukdomar - andra nervsystemet droger - sixmo är indicerat för substitutionsbehandling för opiatberoende i kliniskt stabila vuxna patienter som kräver inte mer än 8 mg/dag för sublingual buprenorfin, inom ramen för medicinsk, social och psykologisk behandling.

Europeiska unionen - svenska - EMA (European Medicines Agency)

plethora pharma solutions limited - lidokain, prilocaine - för tidig utlösning - bedövningsmedel - senstend är indicerat för behandling av primär tidig utlösning hos män.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

bausch health ireland ltd - fingolimodhydroklorid - kapsel, hård - 0,5 mg - fingolimodhydroklorid 0,56 mg aktiv substans; propylenglykol hjälpämne

Europeiska unionen - svenska - EMA (European Medicines Agency)

astrazeneca ab - nirsevimab - immunförsvaret sera och immunglobuliner, - beyfortus is indicated for the prevention of respiratory syncytial virus (rsv) lower respiratory tract disease in neonates and infants during their first rsv season. beyfortus should be used in accordance with official recommendations.

Europeiska unionen - svenska - EMA (European Medicines Agency)

sanofi winthrop industrie - teriflunomide - multipel skleros - selektiva immunsuppressiva medel - aubagio 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).

Europeiska unionen - svenska - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - linaclotide - irritabelt tarmsyndrom - narkotika för förstoppning - constella är indicerat för symptomatisk behandling av måttligt till svårt irritabelt tarmsyndrom med förstoppning (ibs-c) hos vuxna.

Europeiska unionen - svenska - EMA (European Medicines Agency)

ucb pharma sa - levetiracetam - epilepsi - antiepileptika, - keppra är indicerat som monoterapi vid behandling av partiella anfall med eller utan sekundär generalisering hos patienter från 16 år med ny diagnostiserad epilepsi. keppra är indicerat som tilläggsbehandling:vid behandling av partiella anfall med eller utan sekundär generalisering hos vuxna, barn och spädbarn från en månads ålder med epilepsi, vid behandling av myoklona anfall hos vuxna och ungdomar från 12 års ålder med juvenil myoklona epilepsi, vid behandling av primärt generaliserade tonisk-kloniska anfall hos vuxna och ungdomar från 12 års ålder med idiopatisk generaliserad epilepsi.

Europeiska unionen - svenska - EMA (European Medicines Agency)

biogen netherlands b.v. - dimetylfumarat - multipel skleros - immunsuppressiva - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Europeiska unionen - svenska - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agenter för dermatit, med undantag av kortikosteroider - 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.

Europeiska unionen - svenska - EMA (European Medicines Agency)

ptc therapeutics international limited - eladocagene exuparvovec - aminosyrametabolism, infödda fel - enzymes, other alimentary tract and metabolism products - upstaza is indicated for the treatment of patients aged 18 months and older with a clinical, molecular, and genetically confirmed diagnosis of aromatic l amino acid decarboxylase (aadc) deficiency with a severe phenotype (see section 5.