Examples of using Study medication 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
N randomised patients who received at least 1 dose of study medication.
Subjects were continued on their study medication from week 12 to week 55.
received study medication.
The SVR rates for subjects who received at least one dose of any study medication(Intent-to-Treat population) are shown in Table 9.
received at least one dose of study medication.
In three studies on the effect of 5 HTP in obese patients, the study medication resulted in decreased food intake with resultant weight loss.
Intent-to-treat: all confirmed events up to the end of the trial included patients potentially exposed to non-study interventions following discontinuation of study medication.
Most of the patients received the study medication on top of conventional therapy including platelet inhibitors, lipid lowering agents and beta-blockers.
efficacy of SIFROL prolonged-release tablets, patients were instructed to take study medication without regard to food intake.
Most of the patients received the study medication on top of conventional therapy including platelet inhibitors, lipid lowering agents and beta-blockers.
2,530 received other study medications in 8 active and placebo-controlled phase III clinical trials.
Patients who received at least one dose of study medication and who had a positive culture for Candida species from a normally sterile site before study entry were included in the modified intent.
stabilise disease prior to randomisation to blinded study medication for 52 weeks.
withdrew study medication due to any reason risk ratio:
stabilise disease prior to randomisation to blinded study medication for 52 weeks.
Investigators were instructed to titrate the study medication to 100 mg daily as appropriate;
group who received 1, 2, or 3 doses of study medication with and without rescue medication. .
Treatment-emergent hepatic AEs resulted in permanent discontinuation of study medication for 50 subjects(21.4%)
The mean pre-dose FEV1(average of the values taken at -45 and -15 minutes prior to the morning dose of study medication) was statistically significant in favour of Ultibro Breezhaler at week 26 compared to fluticasone/salmeterol(100 ml,
They're administering them, They're not studying medication.
They're not studying medication, bobbi. They're administering them.
They're not studying medication, Bobbi. They're administering them, giving mandatory supplements to all their employees.