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  2. Levobunolol - Wikipedia

    en.wikipedia.org/wiki/Levobunolol

    Levobunolol is the pure L-enantiomer of bunolol and has more than 60 times the pharmacological activity of D-bunolol. [3] It is used as the hydrochloride, which melts at 209 to 211 °C (408 to 412 °F) and is soluble in water and methanol and slightly soluble in ethanol. [2]

  3. Betaxolol - Wikipedia

    en.wikipedia.org/wiki/Betaxolol

    Betaxolol is most commonly ingested orally alone or with other medications for the management of essential hypertension. [4] It is a cardioselective beta blocker, targeting beta-1 adrenergic receptors found in the cardiac muscle.

  4. Bambuterol - Wikipedia

    en.wikipedia.org/wiki/Bambuterol

    Concomitant administration of bambuterol with corticosteroids, diuretics, and xanthine derivatives (such as theophylline) increases the risk of hypokalemia (decreased levels of potassium in the blood).

  5. Levobetaxolol - Wikipedia

    en.wikipedia.org/wiki/Levobetaxolol

    It is marketed as a 0.25 or 0.5% ophthalmic solution of levobetaxolol hydrochloride under the trade name Betaxon. Levobetaxolol is a beta-adrenergic receptor inhibitor ( beta blocker ). Indications

  6. Vernakalant - Wikipedia

    en.wikipedia.org/wiki/Vernakalant

    Vernakalant was initially developed by Cardiome Pharma, and the intravenous formulation was bought for further development by Merck in April 2009. [5] In September 2012, Merck terminated its agreements with Cardiome and has consequently returned all rights of the drug back to Cardiome, which as of 2018 is known as Correvio Pharma .

  7. Guanfacine - Wikipedia

    en.wikipedia.org/wiki/Guanfacine

    Guanfacine, sold under the brand name Tenex (immediate-release) and Intuniv (extended-release) among others, is an oral alpha-2a agonist medication used to treat attention deficit hyperactivity disorder (ADHD) and high blood pressure.

  8. Clenbuterol - Wikipedia

    en.wikipedia.org/wiki/Clenbuterol

    [20] Clenbuterol is a growth-promoting drug in the β agonist class of compounds. It is not licensed for use in China, [21] the United States, [20] or the EU [22] for food-producing animals, but some countries have approved it for animals not used for food, and a few countries have approved it for therapeutic uses in food-producing animals.

  9. Labetalol - Wikipedia

    en.wikipedia.org/wiki/Labetalol

    [20] [21] Intravenously, α to β blockade ratio is 1:7. [ 19 ] [ 16 ] Thus, the labetalol can be thought to be a beta blocker with some α-blocking effects. [ 16 ] [ 18 ] [ 22 ] By comparison, labetalol is a weaker β-adrenergic receptor blocker than propranolol , and has a weaker affinity for α-adrenergic receptors compared to phentolamine .