Examples of using Luminity in English and their translations into Slovak
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How has Luminity been studied?
Other information about Luminity.
How has Luminity been studied?
Patients can also develop a severe allergic reaction to Luminity, and must be closely monitored.
Why has Luminity been approved?
Patients with unstable cardiopulmonary status should be monitored during and for at least 30 minutes following Luminity administration.
Why has Luminity been approved?
Before use, the medicine must be activated by shaking it using a mechanical device called Vialmix,which is supplied to doctors who need to prepare Luminity.
Luminity is for diagnostic use only.
What benefit has Luminity shown during the studies?
Luminity is a gas and solvent for dispersion for injection or infusion.
Therefore, caution should be exercised when Luminity is administered to breast-feeding women.
Luminity 150 microlitres/ml gas and solvent for dispersion for injection/infusion.
As experience is limited in patients with certain severe statesof cardiac and pulmonary diseases, Luminity should be used only after careful consideration and such use should be monitored closely during administration.
Luminity has not been studied in patients with liver or kidney problems, or in the elderly.
During contrast-enhanced echocardiography, serious cardiopulmonary reactions, including fatalities,have occurred during or within 30 minutes of Luminity administration in patients including those with severe cardiac and pulmonary diseases(see section 4.8).
Before activation, Luminity contains a gas, perflutren, and a solution of fatty substances called phospholipids.
Luminity is a solution for dispersion for injection or infusion and is available in a pack containing one or four single-use 1.5 ml vials.
Luminity may be diluted with sodium chloride 9 mg/ml(0.9%) solution for injection or glucose 50 mg/ml(5%) solution for injection.
Luminity is a solution for injection or infusion(drip into a vein) that contains microspheres(tiny bubbles) of perflutren gas as the active substance.
Luminity is given to you before or during your ultrasound examination by healthcare professionals such as doctors who are experienced in this type of examination.
Luminity was effective in enhancing the image of the left ventricle, and it was more effective than placebo in the studies where Luminity and placebo were compared.
As Luminity consists of microspheres that are stable and small enough for transpulmonary passage, enhanced echo signals in the left heart and systemic circulation are obtained.
Luminity is used in adults to obtain a clearer scan of the chambers of the heart, especially of the left ventricle, during echocardiography(a diagnostic test where an image of the heart is obtained using ultrasound).
Luminity is used in patients with suspected or confirmed coronary artery disease(obstruction of the blood vessels supplying the heart muscle), when the image obtained with non- contrast echocardiography is not optimal.
Luminity is used in patients with suspected or confirmed coronary artery disease(obstruction of the blood vessels supplying the heart muscle), when the image obtained with non-contrast echocardiography is not optimal.
Luminity should only be administered by trained physicians with technical expertise in performing and interpreting contrast echocardiograms, and appropriate resuscitation equipment should be available in case of hypersensitivity reactions.
Rats treated with Luminity for 1 month exhibited dose-related, reversible perivascular and peribronchiolar eosinophil infiltration, alveolar macrophage accumulation and increased goblet cell size and number in the lungs.
Luminity should only be given by doctors trained in performing and reading images obtained with contrast echocardiography, in hospitals or clinics where appropriate resuscitation equipment is available in case of allergic reactions.
Luminity should only be administered by trained physicians with technical expertise in performing and interpreting contrast echocardiograms, and appropriate resuscitation equipment should be available in case of cardiopulmonary or hypersensitivity reactions(see section 4.4).