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  2. List of veterinary drugs - Wikipedia

    en.wikipedia.org/wiki/List_of_veterinary_drugs

    This article lists veterinary pharmaceutical drugs alphabetically by name. Many veterinary drugs have more than one name and, therefore, the same drug may be listed more than once. Abbreviations are used in the list as follows: INN = International Nonproprietary Name; BAN = British Approved Name; USAN = United States Adopted Name

  3. Clonidine - Wikipedia

    en.wikipedia.org/wiki/Clonidine

    Clonidine, sold under the brand name Catapres among others, is an α 2A-adrenergic receptor agonist [12] medication used to treat high blood pressure, ADHD, drug withdrawal (e.g., alcohol, opioids, or nicotine), menopausal flushing, diarrhea, spasticity, and certain pain conditions. [13]

  4. Category:Dog medications - Wikipedia

    en.wikipedia.org/wiki/Category:Dog_medications

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  5. 7 Alternatives to Chemotherapy for Lymphoma in Dogs - AOL

    www.aol.com/7-alternatives-chemotherapy-lymphoma...

    1. Ketogenic Diet. Cancer cells rely on glucose for energy to grow. The ketogenic diet is a way to provide an alternative energy source to normal cells in the dog's body while starving the cancer ...

  6. Romifidine - Wikipedia

    en.wikipedia.org/wiki/Romifidine

    Romifidine is a drug that is used in veterinary medicine as a sedative mainly in large animals such as horses, [1] although it may be used in a wide variety of species. [2] [3] It is not used in humans, but is closely related in structure to the commonly used drug clonidine. Romifidine acts as an agonist at the α 2 adrenergic receptor subtype.

  7. Urapidil - Wikipedia

    en.wikipedia.org/wiki/Urapidil

    Urapidil is a sympatholytic antihypertensive drug.It acts as an α 1-adrenoceptor antagonist and as an 5-HT 1A receptor agonist. [1] Although an initial report suggested that urapidil was also an α 2-adrenoceptor agonist, [2] this was not substantiated in later studies that demonstrated it was devoid of agonist actions in the dog saphenous vein and the guinea-pig ileum. [3]

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