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Strong CYP2D6 inhibitors (paroxetine, fluoxetine, quinidine) increase venlafaxine AUC by approximately 60% [3]
These compounds enter via ingestion, inhalation or dermal absorption and primarily accumulate in the GI tract (Hawkins et al., 2020)
Its clinical use is currently limited to a single product, known as pramlintide, which is approved as an adjunct therapy in persons with insulin-treated diabetes
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