ShaunG
Bluelighter
- Joined
- Aug 10, 2011
- Messages
- 272
So my doctor prescribed this for me for sleep as I taper from Xanax. He said not to take it unless I really needed it to sleep. The reviews I have read for using this drug to sleep seem to be pretty decent for an anti-depressant. I have tried several SSRIs for anxiety and couldn't stand any of them which is how i landed on low dose daily Xanax which I am proactively attempting to get off. I know this is an SARI and not an SSRI, but just wanted feedback. I also can't believe that I read mCPP is a metabolite of this drug? wtf is that? i dont want pipes lol...this can't be good for your kidneys...
Wikipedia
Pharmacokinetics
Trazodone is well absorbed after oral administration with mean peak blood levels obtained at approximately 1 hour after ingestion. Absorption is somewhat delayed and enhanced by food. The mean blood elimination half-life is biphasic: the first phase's half-life is 3–6 hours, and the following phase's half-life is 5–9 hours. The drug is extensively metabolized with 3 or 4 major metabolites having been identified in the human body, particularly mCPP,[43] which may contribute to the side effect profile of trazodone. mCPP has been shown to activate numerous serotonin receptors, including 5-HT2C. Approximately 70–75% of 14C-labelled trazodone was found to be excreted in the urine within 72 hours.[44] Trazodone is highly protein-bound.
As a consequence of the production of mCPP as a metabolite, patients administered trazodone may test positive on EMIT II urine tests for the presence of MDMA ("ecstasy").[45]
Wikipedia
Pharmacokinetics
Trazodone is well absorbed after oral administration with mean peak blood levels obtained at approximately 1 hour after ingestion. Absorption is somewhat delayed and enhanced by food. The mean blood elimination half-life is biphasic: the first phase's half-life is 3–6 hours, and the following phase's half-life is 5–9 hours. The drug is extensively metabolized with 3 or 4 major metabolites having been identified in the human body, particularly mCPP,[43] which may contribute to the side effect profile of trazodone. mCPP has been shown to activate numerous serotonin receptors, including 5-HT2C. Approximately 70–75% of 14C-labelled trazodone was found to be excreted in the urine within 72 hours.[44] Trazodone is highly protein-bound.
As a consequence of the production of mCPP as a metabolite, patients administered trazodone may test positive on EMIT II urine tests for the presence of MDMA ("ecstasy").[45]