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[1] [2] [3] Subgroup J01 is part of the anatomical group J Antiinfectives for systemic use. [4] Codes for veterinary use (ATCvet codes) can be created by placing the letter Q in front of the human ATC code: for example, QJ01. [5] ATCvet codes without corresponding human ATC codes are cited with the leading Q in the following list.
carprofen – COX-2 selective NSAID used to relieve pain and inflammation in dogs and cats; cefpodoxime – antibiotic; cephalexin – antibiotic, particularly useful for susceptible Staphylococcus infections; ciprofloxacin – antibiotic of quinolone group
Doxycycline was patented in 1957 and came into commercial use in 1967. [7] [8] It is on the World Health Organization's List of Essential Medicines. [9] Doxycycline is available as a generic medicine. [1] [10] In 2022, it was the 68th most commonly prescribed medication in the United States, with more than 9 million prescriptions. [11] [12]
The term dosage form may also sometimes refer only to the pharmaceutical formulation of a drug product's constituent substances, without considering its final configuration as a consumable product (e.g., capsule, patch, etc.). Due to the somewhat ambiguous nature and overlap of these terms within the pharmaceutical industry, caution is ...
Proligestone is used to control estrus in dogs and cats and has also been used to treat hypersexuality in dogs and cats. [4] Pharmacology ... [1] [2] It is a C14α ...
This is not to be confused with dose regimen, which is a type of drug therapy in which the dose [mg] of a drug is given at a regular dosing interval on a repetitive basis. Continuing the maintenance dose for about 4 to 5 half-lives (t 1/2 ) of the drug will approximate the steady state level. [ 1 ]
Acetaminophen (paracetamol, Tylenol) can cause liver damage in dogs. The toxic dose is 150 mg/kg. [174] Ibuprofen * can cause gastrointestinal irritation, stomach ulcers, and kidney damage in dogs. [175] Naproxen (Aleve)* has a long half-life in dogs and can cause gastrointestinal irritation, anemia, melena (digested blood in feces), and vomiting.
Modified-release dosage is a mechanism that (in contrast to immediate-release dosage) delivers a drug with a delay after its administration (delayed-release dosage) or for a prolonged period of time (extended-release [ER, XR, XL] dosage) or to a specific target in the body (targeted-release dosage). [1]