Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - osimertinib mesilate - karcinoma, nesīkšūnu plaušas - citi antineoplastiskie līdzekļi pārstāvji, proteīnkināzes inhibitori - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - metformīns hidrohlorīds, dapagliflozin propāndiola monohidrāts - cukura diabēts, 2. tips - drugs used in diabetes, combinations of oral blood glucose lowering drugs - xigduo ir norādīts ārstēšanai pieaugušajiem 2. tipa cukura diabēts, kā palīglīdzekli, lai diētu un vingrinājumiem:• pacientiem, nepietiekami kontrolē to maksimāli pieļaujama devu metformīns vienatnē. • kombinācijā ar citām zālēm, lai ārstētu diabēta pacientiem nepietiekami kontrolēta ar metformīnu un šīs zāles• pacientiem, kas jau tiek ārstēti ar kombināciju dapagliflozin un metformīnu kā atsevišķas tabletes. par pētījuma rezultātiem attiecībā uz ogļūdeņražu terapiju, ietekmi uz glycaemic kontroles un sirds un asinsvadu notikumi, un populācijas izpēte, skatīt 4. 4, 4. 5 un 5.

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - saksagliptīns - cukura diabēts, 2. tips - cukura diabēts - add-on combination therapyonglyza is indicated in adult patients aged 18 years and older with type-2 diabetes mellitus to improve glycaemic control:as monotherapy:in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance;as dual oral therapy:in combination with metformin, when metformin alone, with diet and exercise, does not provide adequate glycaemic control;in combination with a sulphonylurea, when the sulphonylurea alone, with diet and exercise, does not provide adequate glycaemic control in patients for whom use of metformin is considered inappropriate;in combination with a thiazolidinedione, when the thiazolidinedione alone with diet and exercise, does not provide adequate glycaemic control in patients for whom use of a thiazolidinedione is considered appropriate;as triple oral therapy:in combination with metformin plus a sulphonylurea when this regimen alone, with diet and exercise, does not provide adequate glycaemic control;as combination therapy with insulin (with or without metformin), when this regimen alone, with diet and exercise, does not provide adequate glycaemic control.

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - benralizumabs - astma - zāles obstruktīvu elpceļu slimību, - fasenra ir norādīts, kā pievienot uz tehniskās apkopes ārstēšana pieaugušiem pacientiem ar smagu eosinophilic astmas nepietiekami kontrolē, neskatoties uz lielu devu inhalējamo kortikosteroīdu plus ilgstošas darbības beta agonistus.

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - nātrija cirkonija cyclosilicate - hiperkalēmija - visi pārējie terapeitiskie produkti - lokelma ir indicēts, lai ārstētu hyperkalaemia pieaugušo pacientu.

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - glycopyrronium, formoterol fumarate dihydrate - plaušu slimība, hroniska obstruktīva - formoterol un glycopyrronium bromide - bevespi aerosphere ir norādīts, kā tehniskās apkopes bronchodilator ārstēšana, lai mazinātu simptomus pieaugušiem pacientiem ar hronisku obstruktīvu plaušu slimību (hops).

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - andexanet alfa - narkotiku lietošanu saistītās blakusparādības un blakusparādības - visi pārējie terapeitiskie produkti - pieaugušiem pacientiem, kas ārstēti ar tiešu faktors xa (fxa) inhibitoru (apixaban vai rivaroxaban), kad pretēja antikoagulācijas ir vajadzīgi, jo apdraud dzīvību vai nekontrolētas asiņošanas.

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - formoterol fumarate dihydrate, glycopyrronium bromide, budesonide - plaušu slimība, hroniska obstruktīva - zāles obstruktīvu elpceļu slimību, - trixeo aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long acting beta2 agonist or combination of a long-acting beta2 agonist and a long acting muscarinic antagonist.

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - acalabrutinib - leikēmija, limfocītu, hroniska, b-šūna - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

astrazeneca ab - moxetumomab pasudotox - leikēmija, matiņu šūna - antineoplastiski līdzekļi - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).