Difference between revisions of "Mianserine-paroxetine"

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(Created page with '{{Drugswitch | from = mianserine | to = paroxetine | stop = * '''Day 0:''' gradually reduce dosage of mianserine to a maximum of 60 mg/ day. * '''Day 1:''' reduce a dosage of...')
 
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| start =   
 
| start =   
 
* '''Day 1:''' simultaneously start paroxetine in a normal dosage of 20 mg/day.
 
* '''Day 1:''' simultaneously start paroxetine in a normal dosage of 20 mg/day.
* '''Day 8:''' stop administration of mianserine and only continue administration of paroxetine only.
+
* '''Day 8:''' stop administration of mianserine and only continue administration of paroxetine.
 
* If necessary, increase the dosage of paroxetine .
 
* If necessary, increase the dosage of paroxetine .
 
| info =  
 
| info =  
 
* Caution with this switch is necessary, because paroxetine slows the metabolism of mianserine via CYP2D6. }}
 
* Caution with this switch is necessary, because paroxetine slows the metabolism of mianserine via CYP2D6. }}

Revision as of 12:59, 6 May 2009

Mianserine
Type Antidepressant
Group other
links
PubChem 4184
PubMed Mianserine
Kompas (Dutch) Mianserine
Wikipedia Mianserine
paroxetine
Type Antidepressant
Group SSRI
links
Medscape paroxetine
PubChem 43815
PubMed paroxetine
Kompas (Dutch) paroxetine
Wikipedia paroxetine

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

Nietinrijdenbord.png Stop mianserine
  • Day 0: gradually reduce dosage of mianserine to a maximum of 60 mg/ day.
  • Day 1: reduce a dosage of 60 mg/day to 30 mg/day.
Eenrichtingbord.png Start paroxetine
  • Day 1: simultaneously start paroxetine in a normal dosage of 20 mg/day.
  • Day 8: stop administration of mianserine and only continue administration of paroxetine.
  • If necessary, increase the dosage of paroxetine .
Infobord.png More information
  • Caution with this switch is necessary, because paroxetine slows the metabolism of mianserine via CYP2D6.
  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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