Actikerall 5 mg/ g / 100 mg/ g Norge - norsk - Statens legemiddelverk

actikerall 5 mg/ g / 100 mg/ g

almirall hermal gmbh - fluorouracil / salisylsyre - liniment, oppløsning - 5 mg/ g / 100 mg/ g

Diprosalic 0.5 mg/ g / 30 mg/ g Norge - norsk - Statens legemiddelverk

diprosalic 0.5 mg/ g / 30 mg/ g

n.v. organon - kloosterstraat - betametasondipropionat / salisylsyre - salve - 0.5 mg/ g / 30 mg/ g

Diprosalic 0.5 mg/ g / 20 mg/ g Norge - norsk - Statens legemiddelverk

diprosalic 0.5 mg/ g / 20 mg/ g

n.v. organon - kloosterstraat - betametasondipropionat / salisylsyre - liniment, oppløsning - 0.5 mg/ g / 20 mg/ g

Dermanolon vet 1.77 mg/ ml / 17.7 mg/ ml Norge - norsk - Statens legemiddelverk

dermanolon vet 1.77 mg/ ml / 17.7 mg/ ml

le vet beheer b.v. - triamcinolonacetonid / salisylsyre - hudspray, oppløsning - 1.77 mg/ ml / 17.7 mg/ ml

Recicort vet 1.77 mg/ ml / 17.7 mg/ ml Norge - norsk - Statens legemiddelverk

recicort vet 1.77 mg/ ml / 17.7 mg/ ml

le vet beheer b.v. - triamcinolonacetonid / salisylsyre - Øredråper, oppløsning - 1.77 mg/ ml / 17.7 mg/ ml

Angiox Den europeiske union - norsk - EMA (European Medicines Agency)

angiox

the medicines company uk ltd - bivalirudin - akutt koronarsyndrom - antithrombotic agents - angiox er indisert som antikoagulant hos voksne pasienter som gjennomgår perkutan koronar intervensjon (pci), inkludert pasienter med st-segment-forhøyet myokardinfarkt (stemi) under primær pci. angiox er også indisert for behandling av voksne pasienter med ustabil angina / ikke-st-segment-elevation myocardial infarction (ua / nstemi) planlagt for påtrengende eller tidlig intervensjon. angiox bør administreres med acetylsalisylsyre og klopidogrel.

Kaletra Den europeiske union - norsk - EMA (European Medicines Agency)

kaletra

abbvie deutschland gmbh co. kg - lopinavir, ritonavir - hiv-infeksjoner - antivirals for systemic use, protease inhibitors - kaletra er angitt i kombinasjon med andre antiretrovirale legemidler til behandling av hiv-1-infiserte voksne, ungdommer og barn i alderen 14 og eldre. valg av kaletra til å behandle protease inhibitor opplevd hiv-1 infiserte pasienter bør være basert på individuelle viral motstand testing og behandling historie av pasienter.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Den europeiske union - norsk - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - klopidogrelhydroklorid - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antithrombotic agents - , , , , 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. , , ,.

VidPrevtyn Beta Den europeiske union - norsk - EMA (European Medicines Agency)

vidprevtyn beta

sanofi pasteur - sars-cov-2 prefusion spike delta tm protein, recombinant (b.1.351 strain) - covid-19 virus infection - vaksiner - vidprevtyn beta is indicated as a booster for active immunisation to prevent covid-19 in adults who have previously received an mrna or adenoviral vector covid-19 vaccine (see sections 4. 2 og 5. 1 in product information document). bruk av denne vaksinen skal være i samsvar med offisielle anbefalinger.

Vumerity Den europeiske union - norsk - EMA (European Medicines Agency)

vumerity

biogen netherlands b.v. - diroximel fumarate (biib098) - multippel sklerose, relapsing-remitting - immunsuppressive - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).