Difference between revisions of "Paroxetine-moclobemide"

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(Created page with '{{Drugswitch | from = paroxetine | to = moclobemide | stop = Depending on the condition of the patient, there are two scenarios possible: # Gradually reduce dosage of paroxeti...')
 
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* Then the administration of moclobemide can be started in normal dosage of 300 mg/day (2 times a day 150 mg).
 
* Then the administration of moclobemide can be started in normal dosage of 300 mg/day (2 times a day 150 mg).
 
| info =  
 
| info =  
* A switch from paroxetine to moclobemide is not obvious, given the necessary prolonged wash-out period in this case.
 
 
* Occurrence of serotonin syndrome is reported when a wash-out period (of one week) is not considered.}}
 
* Occurrence of serotonin syndrome is reported when a wash-out period (of one week) is not considered.}}

Revision as of 11:05, 15 July 2009

paroxetine
Type Antidepressant
Group SSRI
links
Medscape paroxetine
PubChem 43815
PubMed paroxetine
Kompas (Dutch) paroxetine
Wikipedia paroxetine
Moclobemide
Type Antidepressant
Group MAO-I
links
Medscape Moclobemide
PubChem 4235
PubMed Moclobemide
Kompas (Dutch) Moclobemide
Wikipedia Moclobemide

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

Nietinrijdenbord.png Stop paroxetine

Depending on the condition of the patient, there are two scenarios possible:

  1. Gradually reduce dosage of paroxetine to a maximum of 20 mg/day, and then stop administration abruptly.
  2. Phase out paroxetine from 20 mg/day, to 10 mg/day for one week, and then stop administration abruptly.
Eenrichtingbord.png Start moclobemide
  • Both scenarios are followed by a wash-out period of one week.
  • Then the administration of moclobemide can be started in normal dosage of 300 mg/day (2 times a day 150 mg).
Infobord.png More information
  • Occurrence of serotonin syndrome is reported when a wash-out period (of one week) is not considered.
  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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