GABARAN 300 mg Ρουμανία - Ρουμανικά - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

gabaran 300 mg

ranbaxy (u.k.) limited - gabapentinum - caps. - 300mg - antiepileptice alte antiepileptice

GABARAN 400 mg Ρουμανία - Ρουμανικά - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

gabaran 400 mg

ranbaxy (u.k.) limited - gabapentinum - caps. - 400mg - antiepileptice alte antiepileptice

GABARAN 600 mg Ρουμανία - Ρουμανικά - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

gabaran 600 mg

ranbaxy (u.k.) limited - gabapentinum - compr. film. - 600mg - antiepileptice alte antiepileptice

GABALEPT 300 mg Ρουμανία - Ρουμανικά - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

gabalept 300 mg

teva pharmaceutical works private limited company - ungaria - gabapentinum - caps. - 300mg - antiepileptice alte antiepileptice

GABALEPT 400 mg Ρουμανία - Ρουμανικά - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

gabalept 400 mg

teva pharmaceutical works private limited company - ungaria - gabapentinum - caps. - 400mg - antiepileptice alte antiepileptice

Hepcludex Ευρωπαϊκή Ένωση - Ρουμανικά - EMA (European Medicines Agency)

hepcludex

gilead sciences ireland uc - bulevirtide acetate - hepatitis d, chronic - antivirale pentru uz sistemic - hepcludex is indicated for the treatment of chronic hepatitis delta virus (hdv) infection in plasma (or serum) hdv-rna positive adult patients with compensated liver disease.

Copiktra Ευρωπαϊκή Ένωση - Ρουμανικά - EMA (European Medicines Agency)

copiktra

secura bio limited - duvelisib - leukemia, lymphocytic, chronic, b-cell; lymphoma, follicular - agenți antineoplazici - copiktra monotherapy is indicated for the treatment of adult patients with: relapsed or refractory chronic lymphocytic leukaemia (cll) after at least two prior therapies.  follicular lymphoma (fl) that is refractory to at least two prior  systemic therapies.

Xevudy Ευρωπαϊκή Ένωση - Ρουμανικά - EMA (European Medicines Agency)

xevudy

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - seruri imune și imunoglobuline, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.

PreHevbri Ευρωπαϊκή Ένωση - Ρουμανικά - EMA (European Medicines Agency)

prehevbri

vbi vaccines b.v. - hepatita b antigen de suprafață - hepatita b - vaccinuri - prehevbri is indicated for active immunisation against infection caused by all known subtypes of the hepatitis b virus in adults. it can be expected that hepatitis d will also be prevented by immunisation with prehevbri as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection. the use of prehevbri should be in accordance with official recommendations.