TOLERABILITY in Danish translation

• tolerance
• tolerans
• tolerabiliteten
• tolerancen
• hudvenlighed

Examples of using Tolerability in English and their translations into Danish

A Phase IIIb, randomised study to compare the efficacy, tolerability and safety of anagrelide hydrochloride versus hydroxyurea in high-risk patients with essential thrombocythaemia.
En randomiseret fase IIIb undersøgelse til sammenligning af virkning, tolerans og sikkerhed for anagrelid hydroklorid vs hydroxyurea hos højrisikopatienter med essentiel trombocytæmi.

More research into the safety and tolerability of some additives, such as aspartame, would be desirable,
Det er ønskeligt, at der forskes mere i visse tilsætningsstoffers sikkerhed og tolerance, f. eks.

One clinical and three dermatological studies have also been conducted to test the efficacy and tolerability of Eucerin Volume-Filler Concentrate on women between the ages of 40 and 75.
Desuden er et klinisk og tre dermatologiske studier gennemfà ̧rt for at teste Eucerin Volume-Filler Concentrate's effekt og hudvenlighed på kvinder mellem 40 og 75 år.

To assess the safety and tolerability of anagrelide in young(18-50 years) and elderly(≥ 65 years) ET patients.
At vurdere sikkerhed og tolerans for anagrelid hos unge(18- 50 år) og ældre(≥ 65 år) patienter med ET.

No important safety or tolerability difference between rosuvastatin 5 mg and 10 mg is
At der ikke ses at være væsentlig forskel i sikkerheden eller tolerabiliteten af rosuvastatin 5 mg

Risperidone can be administered in flexible doses over a range of 1 to 6 mg per day to optimize each patient' s level of efficacy and tolerability.
Risperidon kan administreres i fleksible doser fra 1 mg til 6 mg daglig for at optimere effekt og tolerance hos den enkelte patient.

Depending on the disease and the tolerability of the drug, the course can last a long time,
Afhængigt af sygdommen og tolerancen af stoffet kan kurset vare lang tid,

Thereafter, based on individual patient response and tolerability, the dose can be further increased in 300 mg/ day increments every 2-3 days up to a maximum dose of 3600 mg/ day.
På baggrund af patientens respons og tolerans, kan dosis derefter øges med en dosistilvækst på 300 mg dagligt hver 2.- 3. dag op til maksimalt 3600 mg dagligt.

the dose increase should be preceded by an evaluation of the individual response and tolerability.
skal øgningen af dosis ledsages af en evaluering af den enkeltes respons og tolerance.

Patients with renal impairment There is no evidence of a reduction in tolerability associated with an increase in exposure to ibandronate in patients with various degrees of renal impairment.
Patienter med nedsat nyrefunktion Der er ikke påvist, at tolerancen reduceres i forbindelse med en øgning i eksponeringen af ibandronat hos patienter med forskellige grader af nedsat nyrefunktion.

Sufficient data on the tolerability of efavirenz with low-dose ritonavir(100 mg,
Tilstrækkelige data vedrørende tolerans af efavirenz sammen med ritonavir 100 mg i lav dosis(én

constantly increase it if necessary based on individual tolerability and efficiency.
konstant øge den om nødvendigt baseret på individuel tolerance og effektivitet.

There is no evidence of a reduction in tolerability associated with an increase in exposure.
Der er ingen tegn på, at tolerancen reduceres i forbindelsen med en øgning i eksponeringen.

based on careful monitoring of the tolerability.
5 mg dagligt med omhyggelig monitorering af tolerans.

as its pharmacological properties successfully combine with good tolerability in most cases of the drug.
dets farmakologiske egenskaber kombineres med god tolerance i de fleste tilfælde af lægemidlet.

BYETTA therapy should be initiated at 5 µg exenatide per dose administered twice daily(BID) for at least one month in order to improve tolerability.
BYETTA- behandling kan initieres med 5 µg exenatid pr. dosis indgivet to gange dagligt i mindst en måned for at forbedre tolerancen.

Target whole blood trough concentration recommendations Dosing should primarily be based on clinical assessments of rejection and tolerability in each individual patient aided by whole blood tacrolimus trough level monitoring.
Anbefalede dalværdier for koncentrationer i fuldblod Dosering skal baseres primært på kliniske vurderinger af afstødning og tolerans hos den enkelte patient og ved overvågning af tacrolimusniveauet i blod.

At very high doses, a poor gastric tolerability(gastritis, gastric erosions and/ or vomiting) of clopidogrel was also reported in rat and baboon.
Ved meget høje doser clopidogrel blev der hos rotter og bavianer observeret dårlig gastrisk tolerans gastritis, gastriske erosioner og/ eller opkastning.

To investigate the tolerability of anagrelide and hydroxyurea in short
At undersøge toleransen for anagrelid og hydroxyurea ved kort-

The primary endpoint of the study is safety and tolerability, and secondary endpoints include immunologic responses, as measured by an increase in brachyury-specific T-cells
Det primære endemål for forsøget er sikkerhed og tolerabilitet og sekundære endemål omfatter immunologiske responser målt i stigninger i brachyury-specifikke T-celler