Veyvondi Európska únia - islandčina - EMA (European Medicines Agency)

veyvondi

baxalta innovations gmbh - vonicog alfa - von willebrand sjúkdómar - antihemorrhagics - veyvondi er ætlað í fullorðnir (18 ára og eldri) með von willebrand sjúkdómur (vwd), þegar desmópressín (ddavp) meðferð einn er ófullnægjandi eða ekki ætlað til - meðferð blæðing og skurðaðgerð blæðingar - koma í veg skurðaðgerð blæðingar. veyvondi ætti ekki að vera notuð í meðferð með dreyrasýki.

Apixaban Accord Európska únia - islandčina - EMA (European Medicines Agency)

apixaban accord

accord healthcare s.l.u. - apixaban - venous thromboembolism; stroke; arthroplasty - blóðþurrðandi lyf - prevention of venous thromboembolic events (vte) in adult patients who have undergone elective hip or knee replacement surgery. fyrirbyggja heilablóðfall og almenn stíflu í fullorðinn sjúklinga með ekki-valvular gáttum tif (nvaf), með einum eða fleiri hættu þættir, eins og áður en heilablóðfall eða tímabundin blóðþurrðar árás (tia); aldri stærri 75 ár; háþrýstingur; sykursýki; einkennum hjartabilun (nyha flokki sem stóð ii). meðferð djúpt æð blóðtappa (hjá sjúklingum sem fengu) og í lungum stíflu (pe), og koma í veg fyrir endurteknum hjá sjúklingum sem fengu pe í fullorðnir (sjá kafla 4. 4 fyrir haemodynamically óstöðug pe sjúklingar). prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation (nvaf), with one or more risk factors, such as prior stroke or transient ischaemic attack (tia); age≥ 75 years; hypertension; diabetes mellitus; symptomatic heart failure (nyha class ≥ ii). meðferð djúpt æð blóðtappa (hjá sjúklingum sem fengu) og í lungum stíflu (pe), og koma í veg fyrir endurteknum hjá sjúklingum sem fengu pe í fullorðnir (sjá kafla 4. 4 fyrir haemodynamically óstöðug pe sjúklingar).

Rivaroxaban Viatris (previously Rivaroxaban Mylan) Európska únia - islandčina - EMA (European Medicines Agency)

rivaroxaban viatris (previously rivaroxaban mylan)

mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - blóðþurrðandi lyf - rivaroxaban mylan co-administered with acetylsalicylic acid (asa) alone or with asa plus clopidogrel or ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers.  rivaroxaban mylan co-administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events.  ------prevention of venous thromboembolism (vte) in adult patients undergoing elective hip or knee replacement surgery.  treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and prevention of recurrent dvt and pe in adults. -------adults prevention of stroke and systemic embolism in adult   patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Ertapenem SUN Európska únia - islandčina - EMA (European Medicines Agency)

ertapenem sun

sun pharmaceutical industries (europe) b.v. - natríum ertapenem - bakteríusýkingar - ertapenem - treatmentertapenem sun is indicated in paediatric patients (3 months to 17 years of age) and in adults for the treatment of the following infections when caused by bacteria known or very likely to be susceptible to ertapenem and when parenteral therapy is required (see sections 4. 4 og 5. 1):- intra-abdominal infections- community acquired pneumonia- acute gynaecological infections- diabetic foot infections of the skin and soft tissue (see section 4. 4)preventionertapenem sun is indicated in adults for the prophylaxis of surgical site infection following elective colorectal surgery (see section 4. Íhuga ætti að opinbera leiðsögn á réttri notkun af sýklalyfjum.

Bufomix Easyhaler Innöndunarduft 160 míkróg/4,5 míkróg/skammt Island - islandčina - LYFJASTOFNUN (Icelandic Medicines Agency)

bufomix easyhaler innöndunarduft 160 míkróg/4,5 míkróg/skammt

orion corporation - budesonidum inn; formoterolum fúmarat - innöndunarduft - 160 míkróg/4,5 míkróg/skammt

Bufomix Easyhaler Innöndunarduft 320 míkróg/9 míkróg/skammt Island - islandčina - LYFJASTOFNUN (Icelandic Medicines Agency)

bufomix easyhaler innöndunarduft 320 míkróg/9 míkróg/skammt

orion corporation - budesonidum inn; formoterolum fúmarat - innöndunarduft - 320 míkróg/9 míkróg/skammt

Symbicort forte Turbuhaler Innöndunarduft 320/9 míkróg/skammt Island - islandčina - LYFJASTOFNUN (Icelandic Medicines Agency)

symbicort forte turbuhaler innöndunarduft 320/9 míkróg/skammt

astrazeneca a/s - budesonidum inn; formoterolum fúmarat - innöndunarduft - 320/9 míkróg/skammt

Symbicort mite Turbuhaler Innöndunarduft 80/4,5 míkróg/skammt Island - islandčina - LYFJASTOFNUN (Icelandic Medicines Agency)

symbicort mite turbuhaler innöndunarduft 80/4,5 míkróg/skammt

astrazeneca a/s - budesonidum inn; formoterolum fúmarat - innöndunarduft - 80/4,5 míkróg/skammt

Symbicort Turbuhaler Innöndunarduft 160/4,5 míkróg/skammt Island - islandčina - LYFJASTOFNUN (Icelandic Medicines Agency)

symbicort turbuhaler innöndunarduft 160/4,5 míkróg/skammt

astrazeneca a/s - budesonidum inn; formoterolum fúmarat - innöndunarduft - 160/4,5 míkróg/skammt