Examples of using Bioequivalent in English and their translations into Danish
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Medicine
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Colloquial
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Financial
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Ecclesiastic
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Official/political
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Computer
The capsule and liquid dosage forms are bioequivalent.
And s. c. doses(0.5 mg)are bioequivalent in terms of serum AUCs.
The 50 mg and 150 mg capsules have been shown to be bioequivalent.
The studies showed that Stalevo is bioequivalent to the separate tablets.
Two medicines are bioequivalent when they produce the same levels of the active substance in the body.
Comparable quality and to be bioequivalent to CellCept.
The 150 mg tablet is bioequivalent and dose proportional to the 300 mg tablet with respect to AUC∞, Cmax, and tmax.
Has been shown to have comparable quality and to be bioequivalent to Glivec.
The two formulations were bioequivalent in terms of AUC but not in terms of Cmax.
Shown to have comparable quality and to be bioequivalent to CellCept.
The 4 mg granule formulation is bioequivalent to the 4 mg chewable tablet when administered to adults in the fasted state.
The alendronate component in the FOSAVANCE(70 mg/ 2800 IU)combination tablet is bioequivalent to the alendronate 70 mg tablet.
Aripiprazole orodispersible tablet is bioequivalent to aripiprazole tablets, with a similar rate and extent of absorption.
The alendronate component in the ADROVANCE(70 mg/ 2800 IU)combination tablet is bioequivalent to the alendronate 70 mg tablet.
Olanzapine orodispersible tablet is bioequivalent to olanzapine tablets, with a similar rate and extent of absorption.
In conclusion a Potential Serious Risk to Public Health was no longer identified andthe CHMP concluded that the products are bioequivalent and that the benefit-risk ratio is positive.
Cysteamine bitartrate(CYSTAGON) is bioequivalent to cysteamine hydrochloride and phosphocysteamine.
The Committee for Medicinal Products for Human Use(CHMP) concluded that, in accordance with EU requirements,Oprymea has been shown to have comparable quality and to be bioequivalent to Sifrol.
The CHMP concluded that the products are bioequivalent and that the benefit-risk ratio is positive.
Combivir was shown to be bioequivalent to lamivudine 150 mg and zidovudine 300 mg given as separate tablets, when administered to fasting subjects.
A single 50 mg/ ml injection of Enbrel was found to be bioequivalent to two simultaneous injections of 25 mg/ ml.
Trizivir was shown to be bioequivalent to abacavir 300 mg, lamivudine 150 mg and zidovudine 300 mg given as separate tablets for AUC0-∞ and Cmax.
A component interaction study demonstrated that the exposure(Cmax and AUC)of pseudoephedrine following administration of pseudoephedrine alone was bioequivalent to pseudoephedrine exposure following administration of the Aerinaze tablet.
Since it has been demonstrated that Nifedipine Pharmamatch retard tablets are bioequivalent with the nifedipine containing product Adalat OROS tablets, the Nifedipine Pharmamatch retard tablets are interchangeable with Adalat OROS tablets at all times.
Janumet A bioequivalence study in healthy subjects demonstrated that the Janumet(sitagliptin/ metformin hydrochloride)combination tablets are bioequivalent to co-administration of sitagliptin phosphate and metformin hydrochloride as individual tablets.
The combination product can be considered as bioequivalent to products containing the individual components.
Studies in human volunteers have shown Tandemact to be bioequivalent to the administration of pioglitazone and glimepiride given as separate tablets.
After single doses,nimesulide β-cyclodextrin 400 mg sachets were found bioequivalent to< Nimesulide containing medicinal products> 100 mg sachets, with respect to AUC and Cmax. parameters.
Moreover,< Nimesulide containing medicinal products>200 mg suppositories were found bioequivalent to< Nimesulide containing medicinal products> 100 mg tablets, despite a longer Tmax and a reduced Cmax.
