Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

ucb pharma s.a.   - bimekizumab - псориазис - Имуносупресори - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

teva b.v. - салметерол, флутиказона пропионат - pulmonary disease, chronic obstructive; asthma - Лекарства за обструктивна заболявания на дихателните пътища, - airexar spiromax е показан за употреба само при възрастни на възраст над 18 години. asthmaairexar spiromax is indicated for the regular treatment of patients with severe asthma where use of a combination product (inhaled corticosteroid and long-acting β2 agonist) is appropriate:- patients not adequately controlled on a lower strength corticosteroid combination productor- patients already controlled on a high dose inhaled corticosteroid and long-acting β2 agonist. Хронична обструктивна белодробна болест (ХОББ)spiromax airexar е показан за симптоматично лечение на пациенти с хронична обструктивна белодробна болест с ОФВ1.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

les laboratoires servier - ивабрадин хидрохлорид - angina pectoris; heart failure - Сърдечна терапия - Симптоматично лечение на хронична стабилна ангина пекторис ivabradine е показан за симптоматично лечение на хронична стабилна ангина пекторис в коронарна артерия болест възрастни с нормален синусов ритъм и сърдечната честота ≥ 70 bpm. ivabradine is indicated :in adults unable to tolerate or with a contraindication to the use of beta-blockersor in combination with beta-blockers in patients inadequately controlled with an optimal beta-blocker dose. Лечение на хронична сърдечна недостатъчност ivabradine е посочена в хронична сърдечна недостатъчност nyha ii до iv клас със систолното дисфункция, при пациентите в синусов ритъм и чиито пулс е ≥ 75 bpm, в комбинация със стандартна терапия, включително бета-блокер терапия или Когато терапия с бета-блокер е противопоказано или не понася.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

eli lilly nederland b.v. - тадалафил - Ерективна дисфункция - urologicals - Лечение на еректилна дисфункция. За да бъде ефективен тадалафил, се изисква сексуална стимулация. cialis не е показан за употреба при жени.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

eli lilly nederland b.v. - тадалафил - Хипертония, белодробна - urologicals - adultstreatment of pulmonary arterial hypertension (pah) classified as who functional class ii and iii, to improve exercise capacity (see section 5. Ефикасността е доказана при идиопатична ПАХ (ПАХ) и при ПАÕ, свързана с колагенно съдово заболяване. paediatric populationtreatment of paediatric patients aged 2 years and above with pulmonary arterial hypertension (pah) classified as who functional class ii and iii.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

bayer ag  - варденафил - Ерективна дисфункция - urologicals - Лечение на еректилна дисфункция при възрастни мъже. Ерективната дисфункция е невъзможността да се постигне или поддържа ерекция на пениса, достатъчна за задоволително сексуално представяне. За да levitra е било ефективно, е необходимо сексуално стимулиране . levitra не е показан за употреба от жени.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

viatris limited - тадалафил - Хипертония, белодробна - urologicals - talmanco е показан за лечение на пулмонална артериална хипертония (pah), класифицирани като който функционален клас ii и iii, за подобряване на физическия капацитет. Ефикасността е доказана при идиопатична ПАХ (ПАХ) и при ПАÕ, свързана с колагенно съдово заболяване.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

bayer ag  - варденафил - Ерективна дисфункция - urologicals - Лечение на еректилна дисфункция при възрастни мъже. Ерективната дисфункция е невъзможността да се постигне или поддържа ерекция на пениса, достатъчна за задоволително сексуално представяне. За това за vivanza, за да бъде ефективен, е необходимо сексуално стимулиране . vivanza не е показан за употреба от жени.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - Хемоглобинурия, пароксизма - Селективни имуносупресори - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.

Ευρωπαϊκή Ένωση - Βουλγαρικά - EMA (European Medicines Agency)

chanelle pharmaceuticals manufacturing ltd - имидаклоприд, моксидектин - antiparasitic products, insecticides and repellents, macrocyclic lactones, milbemycins - cats; dogs; ferrets - for cats suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the treatment of ear mite infestation (otodectes cynotis),• the treatment of notoedric mange (notoedres cati),• the treatment of the lungworm eucoleus aerophilus (syn. capillaria aerophila) (adults),• the prevention of lungworm disease (l3/l4 larvae of aelurostrongylus abstrusus),• the treatment of the lungworm aelurostrongylus abstrusus (adults),• the treatment of the eye worm thelazia callipaeda (adults),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis),• the treatment of infections with gastrointestinal nematodes (l4 larvae, immature adults and adults of toxocara cati and ancylostoma tubaeforme). Ветеринарният лекарствен продукт може да бъде използван като част от терапевтичната стратегия за алергичен дерматит при бълхи (fad).  for ferrets suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis).  for dogs suffering from, or at risk from, mixed parasitic infections:• the treatment and prevention of flea infestation (ctenocephalides felis),• the treatment of biting lice (trichodectes canis),• the treatment of ear mite infestation (otodectes cynotis), sarcoptic mange (caused by sarcoptes scabiei var. canis), demodicosis (caused by demodex canis),• the prevention of heartworm disease (l3 and l4 larvae of dirofilaria immitis),• the treatment of circulating microfilariae (dirofilaria immitis),• the treatment of cutaneous dirofilariosis (adult stages of dirofilaria repens)• the prevention of cutaneous dirofilariosis (l3 larvae of dirofilaria repens),• the reduction of circulating microfilariae (dirofilaria repens),• the prevention of angiostrongylosis (l4 larvae and immature adults of angiostrongylus vasorum),• the treatment of angiostrongylus vasorum and crenosoma vulpis,• the prevention of spirocercosis (spirocerca lupi),• the treatment of eucoleus (syn. capillaria) boehmi (adults),• the treatment of the eye worm thelazia callipaeda (adults),• the treatment of infections with gastrointestinal nematodes (l4 larvae, immature adults and adults of toxocara canis, ancylostoma caninum and uncinaria stenocephala, adults of toxascaris leonina and trichuris vulpis). Ветеринарният лекарствен продукт може да бъде използван като част от терапевтичната стратегия за алергичен дерматит при бълхи (fad).