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  2. Tramadol - Wikipedia

    en.wikipedia.org/wiki/Tramadol

    The estimated median effective dose (ED 50) for SERT occupancy hence was 98.1 mg, which was associated with a plasma tramadol level of about 330 ng/mL (1,300 nM). [99] The estimated maximum daily dosage of tramadol of 400 mg (100 mg q.i.d. ) would result in as much as 78.7% occupancy of the SERT (in association with a plasma concentration of ...

  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. Tramadol/paracetamol - Wikipedia

    en.wikipedia.org/wiki/Tramadol/paracetamol

    Tramadol/paracetamol, also known as tramadol/acetaminophen and sold under the brand name Ultracet among others, is a fixed-dose combination medication used for the treatment of moderate to severe pain. [3] [4] It contains tramadol, as the hydrochloride, an analgesic; and paracetamol an analgesic. [3] [4] It is taken by mouth. [3] [4]

  5. Celecoxib/tramadol - Wikipedia

    en.wikipedia.org/wiki/Celecoxib/tramadol

    Celecoxib/tramadol sold under the brand name Seglentis, is a fixed-dose combination of the anti-inflammatory celecoxib and the opioid tramadol used for the management and treatment of pain. [ 1 ] Developed by Spanish pharmaceutical company Esteve , it was approved for medical use in the United States in October 2021.

  6. 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 ...

  7. Paracetamol - Wikipedia

    en.wikipedia.org/wiki/Paracetamol

    Paracetamol's bioavailability is dose-dependent: it increases from 63 % for 500 mg dose to 89 % for 1000 mg dose. [6] Its plasma terminal elimination half-life is 1.9–2.5 hours, [ 6 ] and volume of distribution is roughly 50 L. [ 132 ] Protein binding is negligible, except under the conditions of overdose, when it may reach 15–21 %. [ 6 ]

  8. Dirty drug - Wikipedia

    en.wikipedia.org/wiki/Dirty_drug

    In pharmacology, a dirty drug is an informal term for drugs that may bind to many different molecular targets or receptors in the body, and so tend to have a wide range of effects and possibly adverse drug reactions.

  9. List of Schedule IV controlled substances (U.S.) - Wikipedia

    en.wikipedia.org/wiki/List_of_Schedule_IV...

    This is the list of Schedule IV controlled substances in the United States as defined by the Controlled Substances Act. [1] The following findings are required for substances to be placed in this schedule: [2]