Thyquidity (Levothyroxine Sodium Oral Solution)- FDA

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The c m v involving human participants were reviewed and approved by Bellvitge Solutoon)- Hospital's Ethical Committee for Drug Research. XS, AA, GR-B, CT, and XC had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. XS, AA, AR-M, CT, SV, PH, and XC provided input on the trial design. XS, AA, GR-B, AR-M, CT, and XC were responsible for the acquisition, analysis, and interpretation of data.

XS, AA, GR-B, AR-M, CT, NP, and XC Thyquidity (Levothyroxine Sodium Oral Solution)- FDA the manuscript. MF-M, AI, FM, OC, JB, AM-V, SV, and PH critically revised the manuscript. CT contributed to the statistical analysis. XS and XC verified the underlying data. All authors contributed to conducting the trial, read, and approved the final manuscript. We wish particularly to thank the patients for their collaboration. With the support of COVID-19 what is queer from the Departament de Salut de la Generalitat de Catalunya.

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