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The follow up period used to examine outcomes irrespective of ongoing use of the medication (emulating a modified intention-to-treat analysis of a clinical trial), started from the index date, and continued until study end (October 30, 2021), death, or initiation of a GLP1-RA in the DPP4i group, whichever came first (Fig

All synedica formulationsincluding synedica tirzepatide 40mg and retatrutide synedica are synthesised to a minimum purity level of 99.2%

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