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  2. Atipamezole - Wikipedia

    en.wikipedia.org/wiki/Atipamezole

    Atipamezole, sold under the brand name Antisedan among others, is a synthetic α 2 adrenergic receptor antagonist used for the reversal of the sedative and analgesic effects of dexmedetomidine and medetomidine in dogs. Its reversal effect works by competing with the sedative for α 2-adrenergic receptors and displacing them.

  3. Maropitant - Wikipedia

    en.wikipedia.org/wiki/Maropitant

    Side effects in dogs and cats include hypersalivation, diarrhea, loss of appetite, and vomiting. [11] [15] Eight percent of dogs taking maropitant at doses meant to prevent motion sickness vomited right after, likely due to the local effects maropitant had on the gastrointestinal tract. Small amounts of food beforehand can prevent such post ...

  4. Life extension - Wikipedia

    en.wikipedia.org/wiki/Life_extension

    Researchers are also exploring ways to mitigate side-effects from such substances (possibly most notably rapamycin and its derivatives) such as via protocols of intermittent administration [114] [106] [105] [115] [116] and have called for research that helps determine optimal treatment schedules (including timing) in general.

  5. Rabeprazole - Wikipedia

    en.wikipedia.org/wiki/Rabeprazole

    Common side effects include constipation, feeling weak, and throat inflammation. [6] Serious side effects may include osteoporosis, low blood magnesium, Clostridioides difficile infection, and pneumonia. [6] Use in pregnancy and breastfeeding is of unclear safety. [1] It works by blocking H + /K +-ATPase in the parietal cells of the stomach. [6]

  6. Sucralfate - Wikipedia

    en.wikipedia.org/wiki/Sucralfate

    The most common side effect seen is constipation (2–3%). Less commonly reported side effects (<0.5%) include flatulence, headache, hypophosphatemia, xerostomia (dry mouth), and bezoar formation. [24] [25] [26] Use of this drug is not recommended for people with chronic kidney failure, as it might cause aluminium accumulation and toxicity.

  7. Naloxegol - Wikipedia

    en.wikipedia.org/wiki/Naloxegol

    Chemically, naloxegol is a pegylated (polyethylene glycol-modified) derivative of α-naloxol.Specifically, the 6-α-hydroxyl group of α-naloxol is connected via an ether linkage to the free hydroxyl group of a monomethoxy-terminated n=7 oligomer of PEG, shown extending at the lower left of the molecule image at right.

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