Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

abacus medicine a/s - montelukastnatrium - granulat - 4 mg - mannitol hjälpämne; montelukastnatrium 4,16 mg aktiv substans

Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

ct arzneimittel gmbh - montelukastnatrium - tuggtablett - 4 mg - mannitol hjälpämne; aspartam hjälpämne; montelukastnatrium 4,15 mg aktiv substans - montelukast

Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

laboratoire aguettant - fenylefrinhydroklorid - injektionsvätska, lösning i förfylld spruta - 50 mikrogram/ml - fenylefrinhydroklorid 60,9 mikrog aktiv substans

Euroopan unioni - ruotsi - EMA (European Medicines Agency)

sanofi winthrop industrie - klopidogrelvätesulfat - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - antitrombotiska medel - secondary prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six 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 patients undergoing percutaneous coronary intervention (including patients undergoing a stent replacement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic 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. förebyggande av atherothrombotic och tromboemboliska händelser i samband med fibrillationin vuxna patienter med förmaksflimmer som har minst en riskfaktor för vaskulära händelser, är inte lämpliga för behandling med vitamin-k-antagonister och som har låg risk för blödning, clopidogrel är indicerat i kombination med asa för förebyggande av atherothrombotic och tromboemboliska händelser, inklusive stroke.

Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

biogaran - brimonidintartrat - Ögondroppar, lösning - 2 mg/ml - brimonidintartrat 2 mg aktiv substans; bensalkoniumklorid hjälpämne

Euroopan unioni - ruotsi - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinuri, paroxysmal - selektiva immunsuppressiva medel - 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.

Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

abboxia ab - tiopentalnatrium - pulver till injektionsvätska, lösning - tiopentalnatrium 1 g aktiv substans

Euroopan unioni - ruotsi - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - cd19-directed genetically modified autologous cell-based product consisting of purified cd8+ t-cells (cd8+ cells), cd19-directed genetically modified autologous cell-based product consisting of purified cd4+ t cells (cd4+ cells) - lymphoma, large b-cell, diffuse; lymphoma, follicular; mediastinal neoplasms - antineoplastiska medel - breyanzi is indicated for the treatment of adult patients with diffuse large b-cell lymphoma (dlbcl), high grade b-cell lymphoma (hgbcl), primary mediastinal large b-cell lymphoma (pmbcl) and follicular lymphoma grade 3b (fl3b), who relapsed within 12 months from completion of, or are refractory to, first-line chemoimmunotherapy.

Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

krka d.d., novo mesto - fipronil - kutan spray, lösning - 2,5 mg/ml - fipronil 2,5 mg aktiv substans - fipronil - hund, katt

Ruotsi - ruotsi - Läkemedelsverket (Medical Products Agency)

krka d.d., novo mesto - fipronil - kutan spray, lösning - 2,5 mg/ml - fipronil 2,5 mg aktiv substans - fipronil - hund, katt