VarroMed Evrópusambandið - íslenska - EMA (European Medicines Agency)

varromed

beevital gmbh - oxalsýru tvíhýdrat, maurasýru - ectoparasiticides fyrir baugi nota, meðtalin. skordýraeitur - býflugur - meðferð á bláæðasegareki (varroa destructor) í býflugum af býflugur með og án nautgripa.

Sonata Evrópusambandið - íslenska - EMA (European Medicines Agency)

sonata

meda ab - zaleplon - svefntruflun og viðhald - psycholeptics - sonata er ætlað til meðferðar hjá sjúklingum með svefnleysi sem eiga erfitt með að sofna. Það er ætlað aðeins þegar röskun er alvarlegt, slökkva eða láta einstaka til mikillar neyð.

Rivaroxaban Viatris (previously Rivaroxaban Mylan) Evrópusambandið - íslenska - 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.

Dymista Nefúði, dreifa 137 míkróg / 50 míkróg/skammt Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dymista nefúði, dreifa 137 míkróg / 50 míkróg/skammt

viatris aps - azelastinum hýdróklóríð; fluticasonum própíónat - nefúði, dreifa - 137 míkróg / 50 míkróg/skammt

EpiPen Stungulyf, lausn 300 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

epipen stungulyf, lausn 300 míkróg

viatris aps - adrenalinum (epinephrinum inn) - stungulyf, lausn - 300 míkróg

EpiPen Jr. Stungulyf, lausn 150 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

epipen jr. stungulyf, lausn 150 míkróg

viatris aps - adrenalinum (epinephrinum inn) - stungulyf, lausn - 150 míkróg

Imurel Filmuhúðuð tafla 25 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

imurel filmuhúðuð tafla 25 mg

aspen pharma trading limited - azathioprinum inn - filmuhúðuð tafla - 25 mg

Imurel Filmuhúðuð tafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

imurel filmuhúðuð tafla 50 mg

aspen pharma trading limited - azathioprinum inn - filmuhúðuð tafla - 50 mg

Norgesic 35 mg/450 mg Tafla 35+450 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

norgesic 35 mg/450 mg tafla 35+450 mg

viatris aps - orphenadrinum cítrat; paracetamolum inn - tafla - 35+450 mg

Puri-nethol Tafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

puri-nethol tafla 50 mg

aspen pharma trading limited - mercaptopurinum inn - tafla - 50 mg