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Difference between revisions of "Bupropion-clomipramine"

 
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| to = clomipramine  
 
| to = clomipramine  
 
| stop =  
 
| stop =  
* '''Before day 1:''' Gradually reduce dosage of bupropion to a maximum of 150 mg/ day.
+
{{stopBupropion}}
* '''Day 1:''' Stop administration of bupropion
+
| start =  
| start =
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* '''Day 1:''' start administration of clomipramine in a low dosage of 37,5mg/day.  
* '''Day 1-3:''' start administration of clomipramine the next day in a low dosage of 25-50 mg/day.
+
* '''Day 8:''' increase dosage of clomipramine to a dosage of 75 mg/day.
* '''Day 4:''' increase dosage of clomipramine to 75 mg/day and continue slowly increasing the dosage depending on the condition of the patient.
 
 
| info =   
 
| info =   
 
* Bupropion slows the metabolism of clomipramine via CYP2D6.
 
* Bupropion slows the metabolism of clomipramine via CYP2D6.
* Caution is necessary at the start of administration of clomipramine.
 
 
* {{RiskSeizureBupropionTCA}}
 
* {{RiskSeizureBupropionTCA}}
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* {{TCAplasmalevelmonitoring}}
 
}}
 
}}

Latest revision as of 10:55, 4 August 2023

Bupropion
Type Antidepressant
Group other
links
ATC-code N06AX12
Medscape Bupropion
PubChem 444
PubMed Bupropion
Kompas (Dutch) Bupropion
Wikipedia Bupropion
Clomipramine
Type Antidepressant
Group TCA
links
ATC-code N06AA04
Medscape Clomipramine
PubChem 2801
PubMed Clomipramine
Kompas (Dutch) Clomipramine
Wikipedia Clomipramine

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

Nietinrijdenbord.png Stop bupropion
  • Day 1: Stop bupropion.
  • bupropion can be stopped abruptly for every dosage.[3]
Eenrichtingbord.png Start clomipramine
  • Day 1: start administration of clomipramine in a low dosage of 37,5mg/day.
  • Day 8: increase dosage of clomipramine to a dosage of 75 mg/day.
Infobord.png More information
  • Bupropion slows the metabolism of clomipramine via CYP2D6.
  • 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.
  • Plasma monitoring for TCA's is advisable, because of plasma-reponse relations, genetic polymorphism and under or overdosing.[4]
  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.
  3. Multidisciplinair document Afbouwen Overige Antidepressiva 2023
  4. (dutch) monografie.org tricyclische-antidepressiva
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