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Participants who received tranylcypromine were more likely to exit the trial early and more likely to exit because of side effects. Possible reasons for this result include a lower comfort level with tranylcypromine treatment, among both participants and clinicians; a lower tolerance of, or slower accommodation to, tranylcypromine-associated side effects; and the loss of five participants from the tranylcypromine group during the 2-week washout period. Previous studies of tranylcypromine for treatment-resistant depression suggest that using doses higher than the FDA-recommended maximum may produce better outcomes 8, 9.


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