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  2. Tramadol - Wikipedia

    en.wikipedia.org/wiki/Tramadol

    Of these, desmetramadol (O-desmethyltramadol) is the most significant, since it has 200 times the μ-affinity of (+)-tramadol, and furthermore has an elimination half-life of 9 hours, compared with 6 hours for tramadol itself. As with codeine, in the 6% of the population who have reduced CYP2D6 activity (hence reducing metabolism), a reduced ...

  3. Equianalgesic - Wikipedia

    en.wikipedia.org/wiki/Equianalgesic

    An equianalgesic chart can be a useful tool, but the user must take care to correct for all relevant variables such as route of administration, cross tolerance, half-life and the bioavailability of a drug. [5] For example, the narcotic levorphanol is 4–8 times stronger than morphine, but also has a much longer half-life. Simply switching the ...

  4. Tapentadol - Wikipedia

    en.wikipedia.org/wiki/Tapentadol

    Tramadol has several enantiomers, and each forms metabolites after processing in the liver. These tramadol variants have varying activities at the μ-opioid receptor, the norepinephrine transporter, and the serotonin transporter, and differing half-lives, with the metabolites having the best activity. Using tramadol as a starting point, the ...

  5. Absorption rate constant - Wikipedia

    en.wikipedia.org/wiki/Absorption_rate_constant

    The absorption rate constant K a is a value used in pharmacokinetics to describe the rate at which a drug enters into the system. It is expressed in units of time −1. [1] The K a is related to the absorption half-life (t 1/2a) per the following equation: K a = ln(2) / t 1/2a.

  6. Extended-release morphine - Wikipedia

    en.wikipedia.org/wiki/Extended-release_morphine

    Conversion between extended-release and immediate-release (or "regular") morphine is easier than conversion to or from an equianalgesic dose of another opioid with different half-life, with less risk of altered pharmacodynamics.

  7. Benzodiazepine - Wikipedia

    en.wikipedia.org/wiki/Benzodiazepine

    A benzodiazepine can be placed into one of three groups by its elimination half-life, or time it takes for the body to eliminate half of the dose. [196] Some benzodiazepines have long-acting active metabolites, such as diazepam and chlordiazepoxide, which are metabolised into desmethyldiazepam. Desmethyldiazepam has a half-life of 36–200 ...

  8. Oxazepam - Wikipedia

    en.wikipedia.org/wiki/Oxazepam

    [26] [27] The half-life of oxazepam is between 6 and 9 hours. [5] [4] [28] It has been shown to suppress cortisol levels. [29] Oxazepam is the most slowly absorbed and has the slowest onset of action of all the common benzodiazepines according to one British study. [30]

  9. Rebound effect - Wikipedia

    en.wikipedia.org/wiki/Rebound_effect

    The rebound effect, or pharmaceutical rebound phenomenon, is the emergence or re-emergence of symptoms that were either absent or controlled while taking a medication, but appear when that same medication is discontinued, or reduced in dosage.