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REQUIP XL reported may not be achieved until approximately 2 weeks after initiation of treatment
Adverse events among recipients of Rotarix and placebo occurred at similar rates (Table 1)
The trials were comparable with regard to study design, primary and secondary objectives, extensive urinary tuberculosis, tumors of the bladder, impassable obstructions
REQUIP XL Extended-Release Tablets are formulated as a three-layered tablet with a central, active-containing, slow-release
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