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FDA, the Food and Drug Administration, they looked at presentations from Moderna and Pfizer and what they said is, you know, that's all well and good, but even within Omicron, we have all these subvariants right

Given the initial safety and efficacy outcomes and potential for patient benefit relative to the risk of adverse events and given the shortage of donor tissue, the present results motivate the need for randomized, controlled studies

Laboratory reference ranges can vary between NHS trusts and private facilities, so it is essential to interpret results in the context of the specific laboratory's normal values

Ataga et al