Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - vacciner - vaxzevria is indicated for active immunisation to prevent covid 19 caused by sars cov 2, in individuals 18 years of age and older. användning av detta vaccin bör ske i enlighet med officiella rekommendationer.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

taw pharma (ireland) limited - klopidogrelhydroklorid - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antitrombotiska medel - , , , , secondary prevention of atherothrombotic events, , clopidogrel is indicated in: , - adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. , - adult patients suffering from acute coronary syndrome:,    - non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa). ,     - st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy. , , in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic stroke (is), clopidogrel in combination with asa is indicated in:, - adult patients with moderate to high-risk tia (abcd2  score ≥4) or minor is (nihss  ≤3) within 24 hours of either the tia or is event.  , , prevention of atherothrombotic and thromboembolic events in atrial fibrillation, in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. , , for further information please refer to section 5. , , ,.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

gsk vaccines s.r.l. - meningokockgrupp a, c, w-135 och y-konjugatvaccin - immunization; meningitis, meningococcal - bakteriella vacciner - vialsmenveo är indicerat för aktiv immunisering av barn från två års ålder), ungdomar och vuxna med risk för exponering för neisseria meningitidis grupp a, c, w135 och y, för att förhindra att invasiva sjukdomar. användning av detta vaccin bör ske i enlighet med officiella rekommendationer.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir - hiv-infektioner - antivirala medel för systemisk användning - prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adult and paediatric patients from the age of 3 years and at least 15 kg body weight. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). in deciding to initiate treatment with prezista co administered with cobicistat or low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista 75 mg, 150 mg, and 600 mg tablets may be used to provide suitable dose regimens:for the treatment of hiv 1 infection in antiretroviral treatment (art) experienced adult patients, including those that have been highly pre treated. for the treatment of hiv 1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. in deciding to initiate treatment with prezista co administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). prezista 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv 1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are:antiretroviral therapy (art) naïve. art experienced with no darunavir resistance associated mutations (drv rams) and who have plasma hiv 1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 106/l. in deciding to initiate treatment with prezista in such art experienced patients, genotypic testing should guide the use of prezista.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

takeda pharma a/s - alogliptin benzoate, metformin hydroklorid - diabetes mellitus, typ 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - vipdomet is indicated in the treatment of adult patients aged 18 years and older with type-2 diabetes mellitus:as an adjunct to diet and exercise to improve glycaemic control in adult patients, inadequately controlled on their maximal tolerated dose of metformin alone, or those already being treated with the combination of alogliptin and metformin;in combination with pioglitazone (i. triple combination therapy) as an adjunct to diet and exercise in adult patients inadequately controlled on their maximal tolerated dose of metformin and pioglitazone;in combination with insulin (i. trippel kombinationsterapi) som ett komplement till diet och motion för att förbättra glykemisk kontroll hos patienter när insulin på en stabil dos och enbart metformin inte ger tillräcklig glykemisk kontroll.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

mylan pharmaceuticals limited - tenofovirdisoproxil - hiv-infektioner - antivirala medel för systemisk användning - hiv-1 infectiontenofovir disoproxil 245 mg filmdragerade tabletter är indicerat i kombination med andra antiretrovirala läkemedel för behandling av hiv-1 infekterade vuxna. hos vuxna, demonstration av förmån av tenofovir disoproxil i hiv-1-infektion baseras på resultaten av en studie i behandling-naiva patienter, inklusive patienter med hög virusmängd (> på 100 000 kopior/ml) och undersökningar som tenofovir disoproxil lades till stabil bakgrund terapi (främst tritherapy) i antiretrovirala pre-behandlade patienter som drabbats av tidig virologisk fel (< 10.000 kopior/ml, med majoriteten av patienter med < och 5000 kopior/ml). tenofovir disoproxil 245 mg filmdragerade tabletter är också indicerat för behandling av hiv-1-infekterade ungdomar, med nrti motstånd eller toxicitet utgör hinder för användningen av första raden agenter, i åldern 12 till < 18 år. valet av tenofovir disoproxil att behandla antiretroviral-erfarna patienter med hiv-1-infektion bör baseras på individuella viral resistens provning och/eller behandling historia av patienter. hepatit b infectiontenofovir disoproxil 245 mg filmdragerade tabletter är indicerat för behandling av kronisk hepatit b hos vuxna med kompenserad leversjukdom, med tecken på aktiv virusreplikation, kvarstående förhöjda alaninaminotransferas (alat) nivåer och histologiska bevis på aktiv inflammation och/eller fibros. bevis på lamivudin-resistenta hepatit b-virus. dekompenserad leversjukdom. tenofovir disoproxil 245 mg filmdragerade tabletter är indicerat för behandling av kronisk hepatit b hos ungdomar 12 till < 18 år ålder med:kompenserad leversjukdom och bevis för att immunförsvaret aktiv sjukdom, jag. aktiv virusreplikation, kvarstående förhöjda alat-nivåer och histologiska bevis på aktiv inflammation och/eller fibros.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

viatris healthcare limited - tolkapon - parkinsons sjukdom - anti-parkinson läkemedel, Övriga dopaminerga medel - tasmar är indicerat i kombination med levodopa / benserazid eller levodopa / karbidopa för patienter med levodopa-känslig idiopatisk parkinsons sjukdom och motoriska fluktuationer, som inte svarat på eller är intoleranta mot andra katekol-o-metyltransferas (comt) hämmare. på grund av risken för potentiellt livshotande, akut leverskada, tasmar ska inte betraktas som en första linjens tilläggsbehandling till levodopa / benserazid eller levodopa / karbidopa. eftersom tasmar ska bara användas i kombination med levodopa / benserazid och levodopa / carbidopa, förskrivning information för dessa levodopa-preparat är också tillämpliga på deras samtidig användning med tasmar.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

mylan pharmaceuticals limited - anagrelide hydroklorid - trombocytemi, essentiell - antineoplastiska medel - anagrelide är indicerat för minskning av förhöjda trombocyter räknas in vid risk för väsentliga thrombocythaemia (et) patienter som är intoleranta mot sina nuvarande behandling eller vars förhöjda trombocyter räknas inte reduceras till en godtagbar nivå genom att deras nuvarande terapi. an at-risk patientan at-risk essential thrombocythaemia patient is defined by one or more of the following features:>60 years of age ora platelet count >1,000 x 10⁹/l ora history of thrombo-haemorrhagic events.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

astrazeneca ab - tixagevimab, cilgavimab - covid-19 virus infection - prevention of covid-19.

Liên Minh Châu Âu - Tiếng Thụy Điển - EMA (European Medicines Agency)

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabetes mellitus, typ 2 - läkemedel som används vid diabetes - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride mylan is indicated in combination with a sulphonylurea (i. - , trippel kombinationsterapi) som ett komplement till kost och motion hos patienter bristfälligt kontrollerad på deras maximal tolererad dos av metformin och en sulphonylurea. sitagliptin/metformin hydrochloride mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.