Origins of veterinary pharmacology date back to the early 1700s in Europe
Materia medica is the study of the physical and chemical characteristics of materials used as medicine
Scientists extracted and synthesized drugs from plant components, bacteria, and animal sources
Most drugs today are made synthetically in laboratories
Pharmaco means drug
Pharmacology is the study of drugs
Therapy means treatment of disease
Pharmacotherapy is the treatment of disease with medicines
Kinetics is the scientific study of motion
Pharmacokinetics is the study of drug motion, which includes absorption, blood levels, distribution, metabolism, and excretion of drugs
Bioavailability is the quantity of drug available for use by the target tissue
Metabolism is the enzymatic breakdown of a drug making it ready for elimination by the body
Excretion is the process by which a drug is eliminated from the body via kidney, respiratory
Chemical name is the exact designation of the chemical structure of a drug as determined by rules of accepted systems of chemical nomenclature
Generic name is an official name given to a drug and it is licensed under this name. All manufacturers of the drug list it by its generic name
Trade name is a name assigned to a product by its manufacturer (registered or not registered) for identification
Effective dose is the amount of the test drug that causes a defined effect in 50% of the animals that receive it
Lethal dose is the amount of the test drug that kills 50% of the animals that receive it
Therapeutic index is the drug dosage or dose that produces the desired effect with minimal or no signs of toxicity
LD 50 / ED 50
Prescription drugs are regulated by authorities like FDA and Pharmacy Board of Trinidad and Tobago
Prescription drugs are limited to use under the supervision of a veterinarian or physician due to potential danger, toxicity concerns, administration difficulty, or other considerations
Prescription drugs are prescribed to animals once a veterinarian/client/patient relationship has been established
Extra-label drugs are drugs used in a manner that is not specifically described on the FDA-approved label
Extra-label drug use is allowed under the Animal Medicinal Drug Use ClarificationAct of 1994 (AMDUCA)
Over-the-counter drugs (OTC drugs) do not have a significant potential for toxicity and do not require special administration
Controlled substances are drugs considered dangerous because of their potential for human abuse or misuse
Controlled substances must be registered annually with the DEA by veterinarians who use or prescribe them
Authorized handlers of controlled substances must keep records of orders, receipts, uses, discards, and thefts of controlled substances for two years following each transaction
New veterinary drugs must go through a series of tests by regulatory bodies like FDA, European Medicines Agency, and Medicine Control Center
There are four major steps in drug development: Synthesis/discovery of a new drug compound, Safety/effectiveness evaluation, Submission and review of the New Animal Drug Application (NADA), Postmarketing surveillance stage
Injectable routes of administration include IV, IM, and SQ
Drugs given IV have rapid onset of action, higher initial body levels of drug, and shorter duration of activity
Drugs given IM have relatively rapid onset of action and longer duration of activity than IV drugs
Drugs given SQ have slower onset of action and longer duration of activity than IV and IM drugs
Inhalation administration introduces drug to the animal by having it breathe the drug into the lungs
Oral administration delivers the drug directly to the animal’s gastrointestinal tract
The dose of a drug is the amount of drugadministered at one time to achieve the desired effect
Loading dose is the initial dose of drug given to get the drug concentration up to the therapeutic range in a very short period of time
Maintenance dose is the dose of drug that maintains or keeps the drug in the therapeutic range