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Patients should always follow the specific instructions provided with any licensed transdermal medication, as optimal sites will vary depending on the formulation's characteristics and the manufacturer's validated application protocols as detailed in the product's Summary of Product Characteristics (SmPC) and Patient Information Leaflet (PIL)

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29 Antiliraglutide Antibodies: In three of the six phase III LEAD trials, anti-liraglutide antibodies were reported and developed as follows: in 9% to 13% of subjects receiving 0.6 mg to 1.8 mg (LEAD-1)