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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. 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.

  4. Fenfluramine/phentermine - Wikipedia

    en.wikipedia.org/wiki/Fenfluramine/phentermine

    Fenfluramine as a single drug was first introduced in the 1970s, but was not popular because it only temporarily reduced weight. [1] A 1984 study found a weight loss of 7.5 kg on average in 24 weeks, as compared to 4.4 kg under placebo. [4]

  5. Menarini - Wikipedia

    en.wikipedia.org/wiki/Menarini

    "Comparison of frovatriptan plus dexketoprofen (25 mg or 37.5 mg) with frovatriptan alone in the treatment of migraine attacks with or without aura: a randomized study". Cephalalgia. 34 (6): 434– 445. doi: 10.1177/0333102413515342. PMID 24363238

  6. Triamterene - Wikipedia

    en.wikipedia.org/wiki/Triamterene

    While there is a lack of randomized controlled trials evaluating the use of triamterene in the treatment of Ménière's disease, the typical treatment is 37.5 mg of triamterene with 25 mg of hydrochlorothiazide 1–2 capsules daily. [25] [26] This recommendation was given a Strength of Recommendation Taxonomy (SORT) grade of C. [citation needed]

  7. Asparaginase - Wikipedia

    en.wikipedia.org/wiki/Asparaginase

    [19] [20] [21] Across all administered dose levels (25 mg/m 2 for the i.m. route of administration and 37.5 mg/m 2 for the i.v. route), JZP-458 exhibited favorable tolerability without any unexpected adverse events (AEs), serious AEs, or AEs of grade 3 or higher. Among the treatment-emergent AEs reported, nausea was the most frequently observed ...

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