Voorbeelden van het gebruik van Controlled studies in het Engels en hun vertalingen in het Nederlands
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Table 1- Adverse Reactions reported in patients treated with alirocumab in pooled controlled studies.
It was used with some success in controlled studies of men suffering from various forms of depression.
The proportion of patients who responded to these injections was similar to that in the key controlled studies.
In a few controlled studies, aggression or adverse,
The following adverse reactions were reported in patients treated with alirocumab in pooled controlled studies.
Four randomized controlled studies were performed in dialysis patients treated with darbepoetin alfa or epoetin at the time of enrollment.
Four randomized controlled studies were performed in dialysis patients treated with darbepoetin alfa or epoetinat the time of enrollment.
their effectiveness has not been established in controlled studies.
Since 1987, therapeutic effects of EMDR have been demonstrated by a range of controlled studies.
Although changes in the plasma concentrations of other AEDs have been reported, controlled studies have shown no evidence that lamotrigine affects the plasma concentrations of concomitant AEDs.
The pivotal controlled studies involved 6,089 patients receiving Humira
In seven double blind controlled studies, a total of 5941 patients(3672 given Ipreziv,
In controlled studies, combination treatment with dexamethasone consistently showed better outcomes in terms of survival
The report says:"We know from controlled studies that exposure to violence can breed violence.
No controlled studies have been conducted to evaluate the pharmacokinetics of ipilimumab in the paediatric population
There are no adequate and well controlled studies on pregnancy outcome with darunavir in pregnant women.
Two randomised controlled studies were conducted in 270 haemodialysis patients
Double-blind, controlled studies have shown that the drug does not have a detrimental effect on male power.
The most common clinical toxicity of VIRAMUNE is rash, with VIRAMUNE attributable rash occurring in 13.6% of patients in combination regimens in controlled studies.
The efficacy and safety of Lucentis have been assessed in three randomised, controlled studies of at least 12 months duration.