Difference between revisions of "Fluvoxamine-dosulepine"
From Psychiatrienet
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| from = fluvoxamine | | from = fluvoxamine | ||
| to = dosulepine | | to = dosulepine | ||
− | | stop = | + | | stop = {{StopSSRI,SNRI}} |
− | {{ | ||
| start = | | start = | ||
− | + | * '''Day 1:''' start administration of dosulepine in a low dosage of 25 mg/day. | |
− | * '''Day 1:''' | + | * '''Day 8:''' increase dosage of dosulepine to a dosage of 75 mg/day. |
− | * '''Day 8:''' | ||
− | |||
| info = | | info = | ||
− | * | + | * fluvoxamine slows the metabolism of dosulepine via CYP2C19 inhibition. |
+ | * {{SSCYPinh}} | ||
+ | * {{TCAplasmalevelmonitoring}} | ||
}} | }} |
Latest revision as of 14:39, 30 June 2023
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Switch medication from fluvoxamine to dosulepine.[1] [2]
- Day 1: Decrease dose to 50%
- Day 8: Stop
- Day 1: start administration of dosulepine in a low dosage of 25 mg/day.
- Day 8: increase dosage of dosulepine to a dosage of 75 mg/day.
- fluvoxamine slows the metabolism of dosulepine via CYP2C19 inhibition.
- Due to CYP inhibition a longer period of time is needed to reach steady state concentration. Please keep in mind when monitoring plasma levels
- Plasma monitoring for TCA's is advisable, because of plasma-reponse relations, genetic polymorphism and under or overdosing.[3]
- ↑ 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.
- ↑ (dutch) monografie.org tricyclische-antidepressiva
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