Examples of using Safety and tolerability in English and their translations into Swedish
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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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Official/political
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Computer
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Programming
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Political
Long-term safety and tolerability.
Safety and tolerability over an extended 12-week period.
Dosing adjustments may be required based on individual safety and tolerability.
Safety and tolerability was evaluated in the entire study population.
The purpose of the trial is to evaluate the safety and tolerability of T20K in humans.
The safety and tolerability of naltrexone/ bupropion should be assessed at regular intervals.
Dose interruptions may be required based on individual safety and tolerability.
Overall, the safety and tolerability of Cinryze are similar in children and adults.
The phase IIa study's primary endpoint was safety and tolerability of the drug candidate.
Safety and tolerability of repeated use of this product within 24 hours has not been characterised.
Dosing delay or discontinuation may be required based on individual safety and tolerability.
However, to know more about the safety and tolerability, the clinical trial needs to be completed.
Dose increase or reduction is recommended based on individual safety and tolerability.
To assess the safety and tolerability of anagrelide in young(18-50 years)
Subsequent dose adjustments should be based on individual safety and tolerability see section 5.2.
The safety and tolerability of vortioxetine have been established in short-
The primary endpoint of the study was to evaluate the safety and tolerability of the RV001 cancer vaccine.
Post marketing data on safety and tolerability across all pazopanib clinical trials
For pNET, dose modification in 12.5 mg steps may be applied based on individual safety and tolerability.
The trial evaluated pharmacokinetics, safety and tolerability, as well as virologic and immunologic responses through 48 weeks.
The Phase 1 study in healthy volunteers will investigate the safety and tolerability of ABBV-0805.
The safety and tolerability findings for fostamatinib observed in the OSKIRA Phase III programme were generally consistent with those previously reported in earlier studies.
The aim of the study is to confirm Rabeximod's therapeutic effect as well as good safety and tolerability.
The purpose of this study is to evaluate the safety and tolerability of CDNF and the implanted drug delivery system.
Dosing interruption and/or dose reduction may be required based on individual safety and tolerability.
The primary objective is to evaluate safety and tolerability and to find the recommended dose for Phase 2.
For GIST and MRCC, dose modifications in 12.5 mg steps may be applied based on individual safety and tolerability.
The primary objective of the trial was to evaluate the safety and tolerability of Aladote® in combination with N-acetylcysteine(NAC).
Temporary dose interruption and/or dose reduction of Zykadia may be required based on individual safety and tolerability.
The aim of the Phase 1 trial is to evaluate safety and tolerability and to establish a recommended dose for a clinical Phase 2 study.