Examples of using Luminity in English and their translations into Romanian
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Ecclesiastic
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Computer
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Programming
How has Luminity been studied?
What is the risk associated with Luminity?
Immediately after activation, Luminity appears as a.
Luminity has not been specifically studied in patients with hepatic impairment.
Luminity is an ultrasound contrast agent that contains tiny gas bubbles.
Luminity 150 microlitres/ ml solution for dispersion for injection or infusion.
It is not known whether Luminity is excreted in human breast milk.
Luminity has no effect on the ability to drive
Immediately after activation, Luminity appears as a milky white dispersion.
Therefore, caution should be exercised when Luminity is administered to breast-feeding women.
Luminity 150 microlitres/ml gas
If you are allergic to perflutren or any of the other ingredients of Luminity.
Luminity should only be administered to such patients after careful risk/benefit assessment.
In two of these studies, Luminity was compared with placebo(a dummy treatment).
Luminity 150 microlitres/ ml solution for dispersion for injection
The perflutren component of Luminity was rapidly cleared from the systemic circulation via the lungs.
Doppler ultrasound measurements were performed with Luminity in conjunction with the pharmacokinetic evaluation of perflutren.
During echocardiography, the perflutren microspheres in Luminity reflect ultrasound waves differently from the surrounding tissues.
Do not use Luminity after the expiry date which is stated on the carton and label.
Patients can also develop a severe allergic reaction to Luminity, and must be closely monitored.