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2. Cefovecin - Wikipedia

   en.wikipedia.org/wiki/Cefovecin

   Cefovecin is an antibiotic of the cephalosporin class, licensed for the treatment of skin infections in cats and dogs. It is marketed by Zoetis under the trade name Convenia. It is used to treat skin infections caused by Pasteurella multocida in cats, and Staphylococcus intermedius and Streptococcus canis in dogs. The advantage of using a long ...

3. List of antibiotics - Wikipedia

   en.wikipedia.org/wiki/List_of_antibiotics

   The following is a list of antibiotics. The highest division between antibiotics is bactericidal and bacteriostatic . Bactericidals kill bacteria directly, whereas bacteriostatics prevent them from dividing.

4. 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

5. FDA Issues Urgent Warning on Dangers of Common Dog Medication

   www.aol.com/lifestyle/fda-issues-urgent-warning...

   The United States Food and Drugs Administration is warning pet owners about a common medication given to pets to treat arthritis. The F.D.A. now says that the drug Librela may be associated with ...

6. Levofloxacin - Wikipedia

   en.wikipedia.org/wiki/Levofloxacin

   Unlike ciprofloxacin, levofloxacin does not appear to deactivate the drug metabolizing enzyme CYP1A2. Therefore, drugs that use that enzyme, like theophylline, do not interact with levofloxacin. It is a weak inhibitor of CYP2C9, [37] suggesting potential to block the breakdown of warfarin and phenprocoumon. This can result in more action of ...

7. CYP1A2 - Wikipedia

   en.wikipedia.org/wiki/CYP1A2

   Following is a table of selected substrates, inducers and inhibitors of CYP1A2. Inhibitors of CYP1A2 can be classified by their potency, such as: Strong inhibitor being one that causes at least a 5-fold increase in the plasma AUC values of sensitive substrates metabolized through CYP1A2, or more than 80% decrease in clearance thereof. [18]

8. Category:CYP1A2 inhibitors - Wikipedia

   en.wikipedia.org/wiki/Category:CYP1A2_inhibitors

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9. Cytochrome P450 (individual enzymes) - Wikipedia

   en.wikipedia.org/wiki/Cytochrome_P450...

   Clozapine, imipramine, paracetamol, phenacetin Heterocyclic aryl amines Inducible and CYP1A2 5-10% deficient oxidize uroporphyrinogen to uroporphyrin (CYP1A2) in heme metabolism, but they may have additional undiscovered endogenous substrates. are inducible by some polycyclic hydrocarbons, some of which are found in cigarette smoke and charred ...