Venlafaxin insättningssymtom
Venlafaxine
Antidepressant medication
Pharmaceutical compound
Pronunciation | VEN-lə-FAK-seen |
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Trade names | Effexor, others[1] |
AHFS/ | Monograph |
MedlinePlus | a |
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Routes of administration | Oral |
Drug class | Serotonin–norepinephrine reuptake inhibitor |
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Bioavailability | 42±15%[2] |
Protein binding | 27±2% (parent compound), 30±12% (active metabolite, desvenlafaxine)[6] |
Metabolism | Extensively metabolised by the liver,[2][6] primarily via CYP2D6[8] |
Metabolites | O-desmethylvenlafaxine (ODV), see desvenlafaxine |
Elimination half-life | 5±2 h (parent compound for immediate release preparations), 15±6 h (parent compound for extended-release preparations), 11±2 h (active metabolite)[2][6] |
Excretion | Kidney (87%; 5% as unchanged drug; 29% as desvenlafaxine and 53% as other metabolites)[2][6] |
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CompTox Dashbo Utredningen som riktar sig mot hälso- samt sjukvårdspersonal, besitter utformats utefter tillgänglig litteratur och tillgångar vid tidpunkten för analys. Innehållet inom utredningen uppdateras inte. Hälso- och sjukvårdspersonal är ansvarig för hur de använder informationen nära rådgivning alternativt behandling från patienter. Utsättningssymtom från venlafaxinFråga: Jag har ett patient liksom haft venlafaxin under flera år samt nu besitter vi trappat ut läkemedlet pga utebliven effekt. beneath egentligen bota nedtrappningen (som skett inneliggande på sjukhus) har patienten haft huvudvärk, yrsel, illamående och ”stötar igenom kroppen”, vilket tolkats som utsättningssymptom. Nu existerar venlafaxin exponerad helt sedan en sju dagar men symptomen finns kvar. Jag fråga vad senaste forskningen säger om venlafaxins nedtrappning, utsättningssymptom och eventuell behandling från dessa? Svar: VenlafaxineBoxed WarningSuicidality and antidepressant drugs: Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use of venlafaxine or any other antidepressant in a child, adolescent, or young adult must balance this risk with the clinical need. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24; there was a reduction in risk with antidepressants compared to placebo in adults aged 65 and older. Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients of all ages who are started on antidepressant therapy should be monitored appropriately and observed closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Venlafaxine is not approved for use in pediatric patients. Dosage FormsExcipie |