Desderman N Литва - литовська - SMCA (Valstybinė vaistų kontrolės tarnyba)

desderman n

schulke & mayr gmbh, robert-koch-str. 2, de-22851 norderstedt (vokietija) - bifenil-2-olis; bifenil-2-olis - veikliosios medžiagos cas nr.: 90-43-7, eb nr.: 201-993-5, veikliosios medžiagos pavadinimas: bifenil-2-olis, koncentracija: 0.1% , veiklioji; veikliosios medžiagos cas nr.: 90-43-7, eb nr.: 201-993-5, veikliosios medžiagos pavadinimas: bifenil-2-olis, koncentracija: 0.1% , veiklioji - asmens higiena

Desderman® N Литва - литовська - SMCA (Valstybinė vaistų kontrolės tarnyba)

desderman® n

schulke & mayr gmbh, robert-koch-str. 2, 22851 norderstedt (vokietija) - etanolis, etilo alkoholis; etanolis, etilo alkoholis - veikliosios medžiagos cas nr.: 64-17-5, eb nr.: 200-578-6, veikliosios medžiagos pavadinimas: etanolis, etilo alkoholis, koncentracija: 78.2% , veiklioji; veikliosios medžiagos cas nr.: 64-17-5, eb nr.: 200-578-6, veikliosios medžiagos pavadinimas: etanolis, etilo alkoholis, koncentracija: 78.2% , veiklioji - asmens higiena

Desderman® pure Литва - литовська - SMCA (Valstybinė vaistų kontrolės tarnyba)

desderman® pure

uab „apiterapija“, lazdynų g. 21, lt-04129 vilnius - bifenil-2-olis; bifenil-2-olis - veikliosios medžiagos cas nr.: 90-43-7, eb nr.: 201-993-5, veikliosios medžiagos pavadinimas: bifenil-2-olis, koncentracija: 0.1% , veiklioji; veikliosios medžiagos cas nr.: 90-43-7, eb nr.: 201-993-5, veikliosios medžiagos pavadinimas: bifenil-2-olis, koncentracija: 0.1% , veiklioji - asmens higiena

Desderman® pure gel Литва - литовська - SMCA (Valstybinė vaistų kontrolės tarnyba)

desderman® pure gel

uab „apiterapija“, lazdynų g. 21, lt-04129 vilnius - bifenil-2-olis; bifenil-2-olis - veikliosios medžiagos cas nr.: 90-43-7, eb nr.: 201-993-5, veikliosios medžiagos pavadinimas: bifenil-2-olis, koncentracija: 0.1% , veiklioji; veikliosios medžiagos cas nr.: 90-43-7, eb nr.: 201-993-5, veikliosios medžiagos pavadinimas: bifenil-2-olis, koncentracija: 0.1% , veiklioji - asmens higiena

Apoquel Європейський Союз - литовська - EMA (European Medicines Agency)

apoquel

zoetis belgium sa - oklacitinib maleatas - dermatito veikėjai, išskyrus kortikosteroidus - Šunys - - treatment of pruritus associated with allergic dermatitis in dogs. - treatment of clinical manifestations of atopic dermatitis in dogs.

Protopic Європейський Союз - литовська - EMA (European Medicines Agency)

protopic

leo pharma a/s - takrolimuzas - dermatitas, atopinis - kiti dermatologiniai preparatai - flare treatmentadults and adolescents (16 years of age and above)treatment of moderate to severe atopic dermatitis in adults who are not adequately responsive to or are intolerant of conventional therapies such as topical corticosteroids. children (two years of age and above)treatment of moderate to severe atopic dermatitis in children (two years of age and above) who failed to respond adequately to conventional therapies such as topical corticosteroids. maintenance treatmentmaintenance treatment of moderate to severe atopic dermatitis for the prevention of flares and the prolongation of flare-free intervals in patients experiencing a high frequency of disease exacerbations (i. pasitaikančių keturis ar daugiau kartų per metus), kurie turėjo pradinis atsakas į šešių savaičių gydymo du kartus per parą, takrolimuzas tepalas (pažeidimų pašalinta, beveik išvalytas arba mažai įtakos).

Dupixent Європейський Союз - литовська - EMA (European Medicines Agency)

dupixent

sanofi winthrop industrie - dupilumabas - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - dermatito veikėjai, išskyrus kortikosteroidus - 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.

Cibinqo Європейський Союз - литовська - EMA (European Medicines Agency)

cibinqo

pfizer europe ma eeig  - abrocitinib - dermatitas, atopinis - kiti dermatologiniai preparatai - cibinqo is indicated for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy.

Ebglyss Європейський Союз - литовська - EMA (European Medicines Agency)

ebglyss

almirall, s.a. - lebrikizumab - dermatitas, atopinis - kiti dermatologiniai preparatai - ebglyss is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older with a body weight of at least 40 kg who are candidates for systemic therapy.