Difference between revisions of "Bupropion-dosulepine"

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| to = dosulepine  
 
| to = dosulepine  
 
| 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 =
+
* '''Day 1:''' start administration of dosulepine in a low dosage of 25 mg/day.  
* '''Day 1-3:''' start administration of dosulepine the next day in a low dosage of 50 mg/day.
+
* '''Day 8:''' increase dosage of dosulepine to a dosage of 75 mg/day.
* '''Day 4:''' increase dosage of dosulepine to 75 mg/day and continue slowly increasing the dosage depending on the condition of the patient.
 
 
| info =   
 
| info =   
 
* Bupropion slows the metabolism of dosulepine via CYP2D6.
 
* Bupropion slows the metabolism of dosulepine via CYP2D6.
* Caution is necessary at the start of administration of dosulepine.
 
 
* {{RiskSeizureBupropionTCA}}
 
* {{RiskSeizureBupropionTCA}}
 +
* {{TCAplasmalevelmonitoring}}
 
}}
 
}}

Latest revision as of 10:59, 4 August 2023

Bupropion
Type Antidepressant
Group other
links
ATC-code N06AX12
Medscape Bupropion
PubChem 444
PubMed Bupropion
Kompas (Dutch) Bupropion
Wikipedia Bupropion
dosulepin
Type antidepressant
Group TCA
links
ATC-code N06AA16
PubChem 13473
PubMed dosulepin
Kompas (Dutch) dosulepin
Wikipedia dosulepin

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

Nietinrijdenbord.png Stop bupropion
  • Day 1: Stop bupropion.
  • bupropion can be stopped abruptly for every dosage.[3]
Eenrichtingbord.png Start dosulepine
  • 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.
Infobord.png More information
  • Bupropion slows the metabolism of dosulepine 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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