Examples of using Ezetimibe in English and their translations into German
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Showing prices on Zetia active ingredient is Ezetimibe.
Ezetimibe, a medicine that inhibits the uptake of cholesterol in the gastrointestinal tract.
Showing prices on Vytorin active ingredient is Simvastatin Ezetimibe.
EZETIMIBE; SIMVASTATIN blocks the body's ability to absorb and make cholesterol.
Your prescriber may decide to temporarily stop taking ezetimibe;
Ezetimibe should be reinfected during acomplia work far if the shikimic goi justifies the fiancee to the fetus.
Are hypersensitive to the active substances simvastatin or ezetimibe;
Patients received either alirocumab 75 mg Q2W or ezetimibe 10 mg once daily in addition to their existing statin therapy.
Repatha significantly reduced LDL-C compared with ezetimibe p< 0.001.
Zetia Ezetimibe Zetia is used to treat high cholesterol(hypercholesterolemia) and sitosterolemia by reducing the amount of cholesterol… more.
Patients received either alirocumab 75 mg Q2W or ezetimibe 10 mg once daily.
Ezetimibe Zetia is used to treat high cholesterol(hypercholesterolemia) and sitosterolemia by reducing the amount of cholesterol your… more.
In parallel Esperionwill submit an NDA for a fixed-dose combination with ezetimibe.
Patients received either alirocumab 75 mg Q2W or ezetimibe 10 mg once daily, or atorvastatin 20 mg once daily as a re-challenge arm.
Strictly follow all instructions provided to you by your physician or pharmacist while using Ezetrol Ezetimibe.
EZETIMIBE blocks the absorption of cholesterol from the stomach. It can help lower blood cholesterol for patients who are at risk of getting heart disease or a stroke.
Repatha significantly reduced LDL-C from baseline to mean of weeks 10 and12 compared with both placebo and ezetimibe p< 0.001.
Fenofibrate, niacin and ezetimibe: When lomitapide was administered to steady state prior to micronised fenofibrate 145 mg, extended release niacin 1000 mg, or ezetimibe 10 mg, no clinically significant effects on the exposure of any of these medicinal products were observed.
On its own, Praluent produced a 24 to 36%greater reduction in blood levels of LDL-cholesterol than ezetimibe.
Key: Q2W once every 2 weeks, QM once monthly, HMD Primary hypercholesterolaemia and mixed dyslipidaemia, a p value< 0.05 when compared with ezetimibe, b p value< 0.001 when compared with ezetimibe, c nominal p value< 0.001 when compared with ezetimibe.
The effect on lipids was similar whether Pelzont was given as monotherapy orwas added to ongoing statin therapy with or without ezetimibe.
Repatha was compared to placebo for the rosuvastatin and simvastatin groups andcompared with placebo and ezetimibe for the atorvastatin group.
In phase 3 studies, 4.8% of patients treated with alirocumab 75 mg and/or 150 mg every 2 weeks exhibited an ADA response after initiating treatment ascompared to 0.6% in the control group placebo or ezetimibe.
A significantly higher proportion of patients achieved an LDL-C of˂70 mg/dL(˂1.81 mmol/L) in the alirocumab groupas compared to placebo or ezetimibe at week 12 and week 24.
The primary efficacy endpoint in all of the phase 3 studies was themean percent reduction from baseline in LDL-C at week 24 as compared to placebo or ezetimibe.
Repatha significantly reduced TC, ApoB, non-HDL-C, TC/HDL-C, ApoB/ApoA1 and Lp(a), from baseline to meanof weeks 10 and 12 compared with both placebo and ezetimibe(p< 0.001) see table 3.
When given on top of standard treatment or on top of placebo, Praluent produced a 24 to 36%greater reduction in blood levels of LDL-cholesterol than ezetimibe.
Repatha significantly reduced LDL-C from baseline to mean of weeks 10 and 12 compared with placebo for the rosuvastatin and simvastatin groups andcompared with placebo and ezetimibe for the atorvastatin group p< 0.001.
DESCARTES was an international, multicentre, double-blind, randomised, placebo-controlled, 52-week study in 901 patients with hyperlipidaemia who received diet alone, atorvastatin,or a combination of atorvastatin and ezetimibe.
Patients receiving Pelzont, nicotinic acid(prolonged-released formulation), or placebo were also taking statins(29% atorvastatin[5-80 mg], 54% simvastatin[10-80 mg], 17% other statins[2.5-180 mg](pravastatin, fluvastatin, rosuvastatin, lovastatin)),of which 9% were also taking ezetimibe 10 mg.