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  2. Tramadol - Wikipedia

    en.wikipedia.org/wiki/Tramadol

    [99] [100] [101] [91] Tramadol does not inhibit the reuptake or induce the release of dopamine. [99] [91] A positron emission tomography imaging study found that single oral 50-mg and 100-mg doses of tramadol to human volunteers resulted in 34.7% and 50.2% respective mean occupation of the serotonin transporter (SERT) in the thalamus. [102]

  3. List of side effects of tramadol - Wikipedia

    en.wikipedia.org/wiki/List_of_side_effects_of...

    Bradycardia; Hypertension (high blood pressure); Allergic reactions (e.g. dyspnoea (shortness of breath), bronchospasm, wheezing, angioneurotic oedema) Anaphylaxis; Changes in appetite

  4. Dexketoprofen - Wikipedia

    en.wikipedia.org/wiki/Dexketoprofen

    Dexketoprofen is a nonsteroidal anti-inflammatory drug (NSAID). It is manufactured by Menarini, under the tradename Keral.It is available in the UK, as dexketoprofen trometamol, as a prescription-only drug and in Latin America as Enantyum, produced by Menarini.

  5. N,O-Didesmethyltramadol - Wikipedia

    en.wikipedia.org/wiki/N,O-didesmethyltramadol

    N,O-Didesmethyltramadol (tramadol metabolite M5) is an opioid derivative which is one of two active metabolites of the opioid analgesic medication tramadol.It is many times less potent than the other active metabolite O-Desmethyltramadol but is still more potent as a mu opioid receptor agonist than tramadol itself, unlike the other metabolites N-desmethyltramadol, N,N-didesmethyltramadol, and ...

  6. Desmetramadol - Wikipedia

    en.wikipedia.org/wiki/Desmetramadol

    (+)-Desmetramadol is a G-protein biased μ-opioid receptor full agonist. [5] It shows comparatively far lower affinity for the δ-and κ-opioid receptors. [6] The two enantiomers of desmetramadol show quite distinct pharmacological profiles; [7] both (+) and (−)-desmetramadol are inactive as serotonin reuptake inhibitors, [8] but (−)-desmetramadol retains activity as a norepinephrine ...

  7. 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 ...

  8. Opioid-induced hyperalgesia - Wikipedia

    en.wikipedia.org/wiki/Opioid-induced_hyperalgesia

    Opioid-induced hyperalgesia (OIH) or opioid-induced abnormal pain sensitivity, also called paradoxical hyperalgesia, is an uncommon condition of generalized pain caused by the long-term use of high dosages of opioids [1] such as morphine, [2] oxycodone, [3] and methadone.

  9. μ-opioid receptor - Wikipedia

    en.wikipedia.org/wiki/Μ-opioid_receptor

    Tramadol and tapentadol carry additional risks associated with their dual effects as SNRIs and can cause serotonin syndrome and seizures. Despite these risks, there is evidence to suggest that these drugs have a lower risk of respiratory depression compared to morphine.

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