Sie suchten nach: reactions were generally mild to moderate (Englisch - Slowakisch)

most of these reactions were mild to moderate.
väčšina z týchto reakcií bola mierna až stredne ťažká.

severity was generally mild to moderate.
závažnosť bola spravidla mierna až stredná.

most reactions were of mild-to-moderate grade.
väčšina reakcií bola mierneho až stredne závažného stupňa.

most adverse reactions were mild to moderate in severity.
väčšina neţiaducich reakcií bola mierna aţ stredne závaţná.

adverse reactions were usually mild to moderate in intensity.
nežiaduce reakcie boli zvyčajne ľahkej až strednej intenzity.

reversible cutaneous reactions have been observed and were generally considered as mild to moderate.
pozorovali sa reverzibilné kožné reakcie, väčšinou sa hodnotili ako mierne až stredne ťažké.

most of the adverse reactions were mild to moderate in intensity.
väčšina nežiaducich účinkov má miernu až stredne závažnú intenzitu.

epistaxis was generally mild to moderate in intensity.
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most adverse reactions were mild to moderate and transient in nature.
väčšina nežiaducich reakcií bola slabá až stredne silná a prechodná.

these reactions were primarily mild to moderate in severity and were reversible.
tieto reakcie boli primárne miernej až stredne závažnej intenzity a boli reverzibilné.

most of these reactions were non-serious, mild to moderate in intensity.
väčšina z týchto reakcií bola nezávažná, miernej až strednej intenzity.

the severity of the adverse events was generally mild to moderate.
nezistili sa žiadne signifikantné rozdiely, keď sa bezpečnostné údaje analyzovali podľa veku, rasy alebo pohlavia.

adverse reactions were transient, self limiting and usually mild to moderate in intensity.
nežiaduce reakcie boli prechodné, obmedzené a zvyčajne miernej až strednej intenzity.

the most common adverse reactions were mild to moderate nausea, dizziness, and headache.
najčastejšie nežiaduce reakcie boli mierna a stredne závažná nauzea, závraty a bolesť hlavy.

adverse reactions were generally of mild to moderate severity and occurred with similar frequency across indications and dosages tested.
vyskytovali sa s podobnou frekvenciou pri všetkých indikáciách a testovaných dávkach.

in the twoplacebo-controlled studies adverse events were generally mild to moderate in severity.
v dvoch placebom kontrolovaných štúdiách boli nežiaduce účinky obyčajne mierne až stredne závažné.

in the two-placebo controlled studies adverse events were generally mild to moderate in severity.
v dvoch placebom kontrolovaných štúdiách boli nežiaduce účinky obyčajne mierne až stredne závažné.

the reports of oedema were generally mild to moderate and usually did not require discontinuation of treatment.
opuchy boli mierne až stredne závažné a zvyčajne si nevyžadovali ukončenie liečby.

overall, these increases were generally mild to moderate and usually did not require discontinuation of treatment.
zvýšenie cholesterolu bolo väčšinou mierne až stredne závažné a zvyčajne si nevyžadovalo prerušenie liečby.

in the two-placebo controlled oral revatio studies adverse events were generally mild to moderate in severity.
v dvoch placebom kontrolovaných štúdiách s perorálnym revatiom boli nežiaduce účinky obyčajne mierne až stredne závažné.