Examples of using Bioequivalent in English and their translations into German
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Ecclesiastic
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Political
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Computer
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Programming
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Official/political
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Political
Ebilfumin hard capsules are bioequivalent formulations.
The 150 mg tablet is bioequivalent and dose proportional to the 300 mg tablet with respect to AUC∞, Cmax, and tmax.
Tamiflu capsules and Tamiflu suspension are bioequivalent formulations.
EVOTAZ is bioequivalent to atazanavir 300 mg once daily in combination with cobicistat 150 mg once daily coadministered as single agents see section 5.2.
Tamiflu suspension and Tamiflu capsules are bioequivalent formulations.
Insulin lispro 200 units/ml solution for injection was bioequivalent to insulin lispro 100 units/ml solution for injection after subcutaneous administration of a single 20 unit dose in healthy subjects.
The company carried out‘bioequivalence'studies to show that Aripiprazole Sandoz is bioequivalent to the reference medicine, Abilify.
Rilpivirine exposures were bioequivalent when comparing Odefsey 200/25/25 mg to one rilpivirine(as hydrochloride) 25 mg film-coated tablet following single dose administration to healthy subjects(n 95) under fed conditions.
A single 50 mg/ mlinjection of Enbrel was found to be bioequivalent to two simultaneous injections of 25 mg/ ml.
The CHMP concluded that, in accordance with EU requirements, Ibandronic Acid Sandoz hasbeen shown to have comparable quality and to be bioequivalent to Bondronat.
A single 50 mg/mlinjection of etanercept was found to be bioequivalent to two simultaneous injections of 25 mg/ml.
The Agency's Committee for Medicinal Products for Human Use(CHMP) concluded that Pheburane has been shown to have comparable quality andto be bioequivalent to Ammonaps.
Lamivudine in the fixed- dose combination tablet was bioequivalent with the lamivudine(single agent) after administration of the individual component.
The alendronate component in the ADROVANCE(70 mg/2,800 IU) combination tablet and the ADROVANCE(70 mg/5,600 IU)combination tablet is bioequivalent to the alendronate 70 mg tablet.
A generic drug can be defined as an identical, or bioequivalent to a brand name drug in its dosage form, safety, strength, route of administration, quality, performance characteristics and intended use.
The CHMP concluded that, in accordance with EU requirements, Ibandronic Acid Teva has been shownto have comparable quality and to be bioequivalent to Bondronat and Bonviva.
In the laboratory study, Cardalis was shown to be bioequivalent to combined treatment with products containing the single active substances medicines are bioequivalent when they produce the same levels of active substance in the body.
CABOMETYX(cabozantinib) tablets and COMETRIQ(cabozantinib) capsules are not bioequivalent and should not be used interchangeably see section 5.2.
In a study in which the potency of ReFacto AF, ReFacto and FVIII activity in patient plasma were measured using the chromogenic substrate assay,ReFacto AF was shown to be bioequivalent to ReFacto.
Bioequivalence studies have shown that vardenafil 10mg orodispersible tablet is not bioequivalent to vardenafil 10 mg film-coated tablets; therefore, the orodispersible formulation should not be used as an equivalent to vardenafil 10 mg film-coated tablets.
The CHMP concluded that, in accordance with EU requirements, Repaglinide Accord has been shown to have comparable quality andto be bioequivalent to the reference medicine.
Because Zalasta is a generic medicine,studies have been limited to tests to demonstrate that it is bioequivalent to the reference medicines i. e. that the medicines produce the same levels of the active substance in the body.
The Committee for Medicinal Products for Human Use(CHMP) concluded that, in accordance with EU requirements,Zalasta has been shown to have comparable quality and to be bioequivalent to Zyprexa and Zyprexa Velotab.
Because Olanzapine Neopharma is a generic medicine,studies have been limited to tests to demonstrate that it is bioequivalent to the reference medicine i. e. that the two medicines produce the same levels of the active substance in the body.
The CHMP concluded that, in accordance with EU requirements, Olazax Disperzi has been shown to have comparable quality andto be bioequivalent to Zyprexa and Zyprexa Velotab.
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.
In an open-label, single-dose, two- treatment, crossover study in healthy volunteers, etanercept administered as a single 50 mg/ml injection was found to be bioequivalent to two simultaneous injections of 25 mg/ ml.