Difference between revisions of "Clomipramine-paroxetine"

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| to = paroxetine
 
| to = paroxetine
 
| stop =  
 
| stop =  
* '''Before day 1:''' gradually reduce dosage of clomipramine to a maximum of 50 mg/day.
+
{{stopClomipramine}}
* '''Day 1:''' reduce dosage of clomipramine to 25 mg/day.
 
* '''Day 8:''' stop clomipramine.
 
 
| start =  
 
| start =  
* '''Day 8:''' start administration of paroxetine in a normal dosage of 20 mg/day.
+
* '''Day 9:''' start administration of paroxetine in a normal dosage of 20 mg/day.
 
| info =  
 
| info =  
* Occurrence of serotonin syndrome is theoretically possible, so caution is necessary.
+
* {{theorSS}}
 
* Paroxetine is a strong inhibitor of CYP2D6, which metabolizes clomipramine.
 
* Paroxetine is a strong inhibitor of CYP2D6, which metabolizes clomipramine.
{{review}}
 
 
}}
 
}}

Latest revision as of 12:02, 4 November 2015

Clomipramine
Type Antidepressant
Group TCA
links
ATC-code N06AA04
Medscape Clomipramine
PubChem 2801
PubMed Clomipramine
Kompas (Dutch) Clomipramine
Wikipedia Clomipramine
paroxetine
Type Antidepressant
Group SSRI
links
Medscape paroxetine
PubChem 43815
PubMed paroxetine
Kompas (Dutch) paroxetine
Wikipedia paroxetine

Switch medication from clomipramine to paroxetine.[1] [2]

Nietinrijdenbord.png Stop clomipramine
  • Before day 1: gradually reduce dosage of clomipramine to a maximum of 75 mg/ day, when this dosage is > 75 mg/day.
  • Day 1-3: reduce dosage of clomipramine to 50 mg/day.
  • Day 4-7: reduce dosage of clomipramine to 25 mg/day.
  • Day 8: stop administration of clomipramine.
Eenrichtingbord.png Start paroxetine
  • Day 9: start administration of paroxetine in a normal dosage of 20 mg/day.
Infobord.png More information
  • Occurrence of the serotonin syndrome is not likely, but theoretically possible, so caution is necessary.
  • Paroxetine is a strong inhibitor of CYP2D6, which metabolizes clomipramine.
  1. 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
  2. Stahl, S. M. (2013). Stahl's essential psychopharmacology: Neuroscientific basis and practical applications (4th ed.). Cambridge University Press.
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