Difference between revisions of "Paroxetine-doxepine"

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| from = paroxetine  
 
| from = paroxetine  
 
| to = doxepin
 
| to = doxepin
| stop =  
+
| stop = {{StopSSRI,SNRI}}
* '''Day 0:''' gradually reduce dosage of paroxetine to a maximum of 20 mg/day when this dosage is > 20 mg/day.
 
* '''Day 1:''' reduce dosage of paroxetine to a maximum of 10 mg/day.
 
* '''Day 8:''' stop dosage of paroxetine.
 
 
| start =  
 
| start =  
Caution is necessary.
+
* '''Day 1:''' start administration of doxepinne in a low dosage of 25mg/day.  
* '''Day 8:''' start administration of doxepin in a low dosage of 25 mg/day.  
+
* '''Day 8:''' increase dosage of doxepine to a dosage of 75 mg/day.
* '''Day 15:''' continue administration of doxepin in a dosage of 50 mg/day.
+
| info =
 
+
* Paroxetine slows the metabolism of doxepine via CYP2D6 inhibition.
 +
* {{SSCYPinh}}
 +
* {{TCAplasmalevelmonitoring}}
 
}}
 
}}

Latest revision as of 14:33, 30 June 2023

paroxetine
Type Antidepressant
Group SSRI
links
Medscape paroxetine
PubChem 43815
PubMed paroxetine
Kompas (Dutch) paroxetine
Wikipedia paroxetine
Doxepin
Type antidepressant
Group TCA
links
ATC-code N06AA12
Medscape Doxepin
PubChem 3158
PubMed Doxepin
Drugs.com doxepin
Kompas (Dutch) Doxepin
Wikipedia Doxepin

Switch medication from paroxetine to doxepin.[2] [3]

Nietinrijdenbord.png Stop paroxetine
  • Day 1: Decrease dose to 50%
  • Day 8: Stop
Eenrichtingbord.png Start doxepin
  • Day 1: start administration of doxepinne in a low dosage of 25mg/day.
  • Day 8: increase dosage of doxepine to a dosage of 75 mg/day.
Infobord.png More information
  • Paroxetine slows the metabolism of doxepine via CYP2D6 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.[4]
  1. 1.0 1.1 1.2 1.3 1.4 KNMP; Informatorium Medicamentorum 2023; Monografie "doxepine" (Dutch)
  2. 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
  3. Stahl, S. M. (2013). Stahl's essential psychopharmacology: Neuroscientific basis and practical applications (4th ed.). Cambridge University Press.
  4. (dutch) monografie.org tricyclische-antidepressiva
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