Примери за използване на Patients who took на Английски и техните преводи на Български
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compared with 1.4 flare-ups in the patients who took placebo.
According to a clinical trial by The Department of Neurology at The University of Gessen in Germany, patients who took butterbur saw a 52% decrease in their migraines.
The cumulative median duration exposure to Votubia(361 patients who took at least one dose of everolimus)
The cumulative median duration of exposure to Votubia(112 patients who took at least one dose of everolimus)
All randomised patients who took at least one dose of double-blind study medication during the short-term double-blind period.
All randomised patients who took at least one dose of double-blind study medicinal product during the shortterm double-blind period.
The Baptist University study found that patients who took Gouteng together with levodopa experienced fewer side effects from the drug while showing a marked improvement in their communication skills.
The other study included 150 patients who took Sifrol for six months,
The following side effects have been reported by patients who took this medicine. You should tell your doctor promptly about these
In the first study, the patients who took Xiaflex along with penile modeling stated that their bother domain score fell by 37% at the end of 52 weeks.
In the third study, after 8 weeks of treatment patients who took Kalydeco had an average improvement of 10.7 percentage points more than those who took placebo.
Patients who took Gouteng together with levodopa experienced fewer side effects from the drug while showing a marked improvement in their communication skills.
After 8 weeks of treatment patients who took Kalydeco had an average improvement of 10.7 percentage points more than those who took placebo.
Patients who took designated treatment as randomised in combination with the correct background treatment
According to reviews of patients who took the drug Neurosystem 7,
The second included 150 patients who took Sifrol for six months,
The studies lasted from four months to two years and involved 1,305 patients who took the combination.
The studies lasted from 4 months to 2 years and involved 1,305 patients who took the combination.
in liver damage assessed in a biopsy, compared with about a quarter of the patients who took placebo.
Among the patients who took Tarceva, the average survival was 8.6 months in those whose tumours were‘EGFR IHC-positive'(had EGFRs on the cell surface),