Difference between revisions of "Dosulepine-bupropion"
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* '''Day 1:''' simultaneously start administration of bupropion in a dosage of 150 mg/day and continue administration of dosulepine according to the scheme above. | * '''Day 1:''' simultaneously start administration of bupropion in a dosage of 150 mg/day and continue administration of dosulepine according to the scheme above. | ||
− | * '''Day 8:''' stop administration of dosulepine and continue administration of bupropion | + | * '''Day 8:''' stop administration of dosulepine and continue administration of bupropion. |
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− | * Bupropion is a strong inhibitor of CYP2D6, which metabolises dosulepine. }} | + | * Bupropion is a strong inhibitor of CYP2D6, which metabolises dosulepine. |
+ | * {{RiskSeizureBupropionTCA}} | ||
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Latest revision as of 16:06, 28 October 2015
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Switch medication from dosulepine to bupropion.[1] [2]
- Before day 1: gradually reduce dosage of dosulepine to a maximum of 75 mg/ day, when this dosage is > 75 mg/day.
- Day 1-3: reduce dosage of dosulepine to 50 mg/day.
- Day 4-7: reduce dosage of dosulepine to 25 mg/day.
- Day 8: stop administration of dosulepine.
- Day 1: simultaneously start administration of bupropion in a dosage of 150 mg/day and continue administration of dosulepine according to the scheme above.
- Day 8: stop administration of dosulepine and continue administration of bupropion.
- Bupropion is a strong inhibitor of CYP2D6, which metabolises dosulepine.
- The concomitant use of bupropion and tricyclic antidepressants (TCAs) may potentiate the risk of seizures. These agents are all epileptogenic and may have additive effects on the seizure threshold.
- ↑ Switches are based on literature references on this page and expert opinions of the authors. The authors have used pharmacokinetic and receptor affinity properties to determine the switch schedules
- ↑ Stahl, S. M. (2013). Stahl's essential psychopharmacology: Neuroscientific basis and practical applications (4th ed.). Cambridge University Press.
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