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Six mice were assigned per dose group.
Patients of the fixed dose group received only predetermined dose.
This study compares a 400-mcg dose (Group I) to an 800-mcg dose (Group II) of buccal misoprostol.
At baseline, 76 women in the high dose group and 82 in the standard dose group reported any LUTS.
The mice were injected with 0 mg (control group), 0.1 mg (low dose group, LD), 0.25 mg (medium dose group, MD), and 0.4 mg (high dose group, HD GOO per mouse.
The mice were injected with 200 μl of FMNPs with the concentrations of 0 mg/ml (control group), 0.1 mg/ml (low dose group, LD), 0.3 mg/ml (medium dose group, MD), and 0.5 mg/ml (high dose group, HD).
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Dr. Bezwoda reported that the high-dose group had fared much better than the controls.
Moreover, nine patients in the high-dose group, 0.4percentt, and none in the low-dose group, suffered from myopathy, a muscle disorder estimated to affect one in 1,000 people who take statins.
Asthma symptoms, like chest tightness or wheezing were reduced by 42percentt among the high-dose group, 40percentt in the low-dose group, and 30percentt in the placebo group.
The enrolled patients were divided into the normal-dose group and low-dose group.
The mice were randomly divided into the blank group, model group, high-dose group, middle-dose group and the low-dose group of TSRDN.
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