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  2. Xylitol - Wikipedia

    en.wikipedia.org/wiki/Xylitol

    Xylitol is poisonous to dogs. [8] Ingesting 100 milligrams of xylitol per kilogram of body weight (mg/kg bw) causes dogs to experience a dose-dependent insulin release; depending on the dose it can result in life-threatening hypoglycemia. Hypoglycemic symptoms of xylitol toxicity may arise as quickly as 30 to 60 minutes after ingestion.

  3. Cefalexin - Wikipedia

    en.wikipedia.org/wiki/Cefalexin

    The U.S. Food and Drug Administration (FDA) has approved it for use in humans and dogs but not for other species. Like other drugs approved for human use, cefalexin may be prescribed by veterinarians for animals in certain situations. [37] Cefalexin (Lexylan) is indicated for the treatment of cattle, dogs, and cats in the European Union. [2]

  4. Penicillin - Wikipedia

    en.wikipedia.org/wiki/Penicillin

    Penicillin molecules are small enough to pass through the spaces of glycoproteins in the cell wall. For this reason Gram-positive bacteria are very susceptible to penicillin (as first evidenced by the discovery of penicillin in 1928 [46]). [47] Penicillin, or any other molecule, enters Gram-negative bacteria in a different manner. The bacteria ...

  5. 6-APA - Wikipedia

    en.wikipedia.org/wiki/6-APA

    6-APA ((+)-6-aminopenicillanic acid) is a chemical compound used as an intermediate in the synthesis of β–lactam antibiotics. The major commercial source of 6-APA is still natural penicillin G. The semi-synthetic penicillins derived from 6-APA are also referred to as penicillins and are considered part of the penicillin family of antibiotics ...

  6. Melting point - Wikipedia

    en.wikipedia.org/wiki/Melting_point

    The melting point (or, rarely, liquefaction point) of a substance is the temperature at which it changes state from solid to liquid. At the melting point the solid and liquid phase exist in equilibrium. The melting point of a substance depends on pressure and is usually specified at a standard pressure such as 1 atmosphere or 100 kPa.

  7. Side effects of penicillin - Wikipedia

    en.wikipedia.org/wiki/Side_effects_of_penicillin

    Destruction of the normal protective flora of beneficial bacteria can occur in dogs and horses. [21] [22] Dogs may have side effects that include: joint pain, loss of appetite, vomiting, flatulence (intestinal gas), fungal infections and digestive problems. [23] Like humans, dogs can have a similar side effect related to developing a serious ...

  8. Monensin - Wikipedia

    en.wikipedia.org/wiki/Monensin

    Monensin is a polyether antibiotic isolated from Streptomyces cinnamonensis. [2] It is widely used in ruminant animal feeds. [2] [3]The structure of monensin was first described by Agtarap et al. in 1967, and was the first polyether antibiotic to have its structure elucidated in this way.

  9. Phenoxymethylpenicillin - Wikipedia

    en.wikipedia.org/wiki/Phenoxymethylpenicillin

    Phenoxymethylpenicillin, also known as penicillin V (PcV) and penicillin VK, is an antibiotic useful for the treatment of a number of bacterial infections. [2] Specifically it is used for the treatment of strep throat, otitis media, and cellulitis. [2] It is also used to prevent rheumatic fever and to prevent infections following removal of the ...