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Patients should be monitored during and for at least 30 minutes after administration
population found that roughly 70% of the non-institutionalized population had 25-hydroxyvitamin D levels below about 30 ng/mL
The US FDA, EMA, UK MHRA, and Health Canada have not authorized them for human therapeutic use
Nausea, changes in skin color, and hormonal effects are only part of the picture
Faced with this huge market potential, many domestic pharmaceutical companies are entering the field, eager to grab a share
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