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Annual review of public health, 38, 295313
After four weeks of treatment, the dose is recommended to be increased to 7.5 mg, administered subcutaneously once weekly
The tricky question there is about balancing incentives for future innovation in this space against near-term sort of maximizing access for patients right now, he said
Food and Drug Administration includes gallbladder disease in the labelled adverse-effect information for these drugs precisely because the signal is real and worth disclosing, not because it is common or usually severe
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