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Like many emerging therapies, Dihexas clinical profile has its gaps: For this reason, Dihexa should always be used with functional lab support and under physician supervision

This approach uses real-world electronic health records to simulate what a randomized clinical trial might show

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FDA was also clear that compounders must immediately begin transitioning patients taking compounded tirzepatide knockoffs to FDA-approved tirzepatide medicines. The FDA originally declared the tirzepatide shortage over in October