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  2. Phentermine - Wikipedia

    en.wikipedia.org/wiki/Phentermine

    [6] [6] Peak concentrations of phentermine are reached 6 hours following oral administration of a dose of 15 mg. [6] The steady-state levels of phentermine with continuous administration have been found to be around 200 ng/mL in clinical studies. [6] The oral bioavailability of phentermine is not affected by intake of a high-fat meal. [6]

  3. Anti-obesity medication - Wikipedia

    en.wikipedia.org/wiki/Anti-obesity_medication

    Phentermine: Substituted amphetamine: Approved for weight management (short-term) 5 kilograms (11 lb) [62] Methamphetamine: Desoxyn Substituted amphetamine: Approved for weight management (short-term) Tirzepatide: Mounjaro/ Zepbound Dual GLP-1 receptor agonist and GIP agonist: Approved for weight management (chronic) [63] 18.4 percent [64]

  4. Fenfluramine/phentermine - Wikipedia

    en.wikipedia.org/wiki/Fenfluramine/phentermine

    Phentermine was not shown to have harmful effects. [1] Fenfluramine acts as a serotonin releasing agent, [2] phentermine as primarily a norepinephrine releasing agent. Phentermine also induces the release of serotonin and dopamine, although to a far lesser extent than it induces the release of norepinephrine. [3]

  5. Phenmetrazine - Wikipedia

    en.wikipedia.org/wiki/Phenmetrazine

    For comparison, dextroamphetamine 3 mg/kg i.p. increased striatal dopamine levels by about 5,000% in rats. [21] On the other hand, the maximal increases in brain dopamine levels with phenmetrazine are similar to those with the proposed dopamine transporter (DAT) "inverse agonists" methylphenidate and cocaine (e.g., ~1,500%). [ 21 ]

  6. Tramadol - Wikipedia

    en.wikipedia.org/wiki/Tramadol

    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 1,220 ng/mL or 4,632 nM). [102] This is close to that of SSRIs, which occupy the SERT by 80% or more. [102]

  7. Phentermine/topiramate - Wikipedia

    en.wikipedia.org/wiki/Phentermine/topiramate

    Phentermine and topiramate was developed by Vivus, a California pharmaceutical company. In December 2009, Vivus, Inc. submitted a new drug application (NDA) to the FDA and on 1 March 2010, Vivus, Inc. announced that the FDA accepted the NDA for review.

  8. Adderall - Wikipedia

    en.wikipedia.org/wiki/Adderall

    Adderall and Mydayis [11] are trade names [note 2] for a combination drug containing four salts of amphetamine.The mixture is composed of equal parts racemic amphetamine and dextroamphetamine, which produces a (3:1) ratio between dextroamphetamine and levoamphetamine, the two enantiomers of amphetamine. [13]

  9. Selective serotonin reuptake inhibitor - Wikipedia

    en.wikipedia.org/wiki/Selective_serotonin...

    Selective serotonin reuptake inhibitors (SSRIs) are a class of drugs that are typically used as antidepressants in the treatment of major depressive disorder, anxiety disorders, and other psychological conditions.

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