Vitamin D deficiency and anemia: a cross-sectional study
Batch: GF-TESA20-B242 Assay Content: 17.30 mg Purity: 99.7 percent Identification by FTIR Spectrum: 987 Identification by Retention Time: 0.991 Molecular Ion Mass Identification: 5135 Da Bacterial Endotoxins: 0.002 EU/mg Total Aerobic Microbial Count: 0 CFU/g Total Yeast and Mold Count: 0 CFU/g Independent elemental impurity analysis confirmed no detectable arsenic, cadmium, cobalt, lead, mercury, nickel or vanadium, with all measured concentrations remaining below the laboratory detection limit
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All original trials included in our analysis have been documented to have adhered to the Good Clinical Practice guidelines and/or the principles of the Declaration of Helsinki
The main benefit of these medications is that, in large randomized controlled trials, there is an observed weight reduction of on average 15% over 18 months of use
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