Примери за използване на Mostly mild to moderate на Английски и техните преводи на Български
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These effects were mostly mild to moderate.
These adverse reactions are mostly mild to moderate.
ADRs were mostly mild to moderate in severity.
When observed during Zinbryta clinical studies,lymphopenia was mostly mild to moderate(≥ 500/mm3).
Adverse events were mostly mild to moderate in severity.
These events consisted predominantly of rash anddermatitis acneiform and were mostly mild to moderate in severity.
Skin reactions are mostly mild to moderate and usually resolve within a few days.
In double-blind controlled clinical trials, application site reactions were mostly mild to moderate in severity.
These reactions were mostly mild to moderate in severity and generally subsided within one to two weeks.
However, only about half of them are typically found to have detectable changes in their cervical cells as a result(mostly mild to moderate).
Adverse reactions were mostly mild to moderate in severity.
Rash was mostly mild to moderate, often occurring within the first four weeks of treatment and resolving with continued dosing.
The most frequently reported adverse reactions were mostly mild to moderate in severity and transient in nature.
Rash was mostly mild to moderate, often occurring within the first four weeks of treatment and resolving with continued dosing(see section 4.4).
The most common infusion-related side effects,which are mostly mild to moderate, are fever, chills, feeling sick and vomiting.
Visual disturbances(< 1%) associated with the use of Ketek, including blurred vision, difficulty focusing and diplopia,were mostly mild to moderate.
Application site reactions were mostly mild to moderate in severity and were rated as severe in less than 2% of patients.
Post-marketing experience of infusion associated reactions revealed reporting of pyrexia,chills and vomiting, mostly mild to moderate in intensity.
These reactions are dosedependent, mostly mild to moderate, generally transient and mostly resolve even if treatment is continued.
Visual disturbances(< 1%) associated with the use of Ketek, including blurred vision, difficulty focusing and diplopia,were mostly mild to moderate, but severe reactions have also been reported.
These GI adverse reactions are mostly mild to moderate in severity, with 0.3% of diarrhoea and 0.3% of nausea reported as severe.
Gastrointestinal reactions like abdominal pain, feeling sick, vomiting and diarrhoea occur in more than 1 in 10 patients(very common),but are mostly mild to moderate and respond well to additional treatment.
In clinical trials, rash was mostly mild to moderate, often occurring within the first four weeks of treatment and resolving with continued dosing.
Injection site reactions were very common, occurring in the vast majority of patients,were mostly mild to moderate in severity and generally subsided within 1-2 weeks post injection.
ADRs were mostly mild to moderate in intensity and almost all occurred during the infusion or during the 2 hours following the infusion(infusion associated reactions, IARs).
The safety profile of Feraccru is considered acceptable,with side effects that are mostly mild to moderate in intensity and in line with those of other iron preparations.
The CPK elevations in the axSpA study were mostly mild to moderate, transient in nature and of unknown clinical significance with no cases leading to withdrawal.
In this study IRESSA exposure did not increase with increasing dose,adverse events were mostly mild to moderate in severity, and were consistent with the known safety profile of IRESSA.
The most frequently reported adverse reactions were mostly mild to moderate in severity and were manageable without the need for modification of doses or discontinuation of therapy.