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VT Pharmacology Ch.1
Romich 2nd edition "A Brief History Of Veterinary Pharmacology"
Question | Answer |
---|---|
What country established the first five veterinary colleges? year? | France 1760s |
What year were veterinary colleges established in America? which state? | 1850s Philadelphia |
What did the establishment of veterinary colleges have to do with the birth of veterinary pharmacology? | These veterinary college were founded as supplements to schools of medicine and the study of physical and chemical characteristics of materials used as medicines. |
What examples come from a mineral source? | sulfur, iron, electrolytes |
What examples come from a botanical source? | digitalis,opioids |
What examples come from an animal source? | insulin, thyroid hormone, lanolin |
What examples come from a synthetic (manmade or engineered) source? | aspirin, steroids, procaine |
What examples come from biological (molds or bacteria) source? | antibiotics, ergot |
What is the FDA's role in drug approval? | The FDA would approve a drug and advise medical professionals of the side effects of the drug. |
What is the FDA's role in drug monitoring? | Monitoring of the FDA-approved drugs continues as long as the drug is on the market so that adverse reactions can be reported and documented for further investigation. |
Describe a veterinarian/client/patient relationship. | Animals need to be seen and examined by a veterinarian, who assumes responsibility for making clinical assessments based on sufficient knowledge about the health of the animals and their need for treatment and follow-up care. |
Explain the difference between C-I , C-II, C-III, C-IV, and C-V drugs. | The higher the drugs schedule, the lower risk of abuse potential. |
What are some examples of Schedule IV (C-IV) drugs? | butorphanol, diazepam, phenobarbital |
What are some examples of Schedule V (C-V) drugs? | codeine cough syrups, buprenophrine, diphenoxylate |
Drug Enforcement Administration (DEA) | enforces the control of these drugs through the Comprehensive Drug Abuse Prevention and Control Act of 1970 |
Extra-Label Drug | the use of a drug in a manner not specifically described on the FDA-approved label |
Food and Drug Administration (FDA) | a government agency to enforce the federal Pure Food and Drugs Act of 1906 |
Kinetics | medical term for the scientific study of motion |
Over-the-Counter (OTC) Drugs | drugs that may be purchased by the client without a prescription |
Pharmacodynamics | studying the mechanisms of action of a drug and understanding the interactions between the chemical components of living systems and the drugs that enter those systems |
Pharmacokinetics | studying the absorption, distribution, biotransformation (metabolism), and excretion of drugs |
Pharmaocology | study of drugs |
Pharmacotherapeutics | study of drug use in the treatment of disease |
Pharmacotherapy | treatment of disease with medicines |
Prescription Drugs (FDA regulates) | limited to use under the supervision of a veterinarian or physician because of their potential danger, toxicity concerns, administration difficulty, or other considerations |
Veterinarian/Client/Patient | animals need to be seen and examined by a veterinarian, who assumes responsibility for making clinical assessments based on sufficient knowledge about the healthy of the animals and their need for treatment and follow-up care |
Biologics (USDA regulates) | therapeutic agents derived from living organisms, such as vaccines, antibodies, and toxoids |
Controlled Substances | drugs considered dangerous because of their potential for human abuse or misuse |
Drug | a substance used to treat, prevent, or diagnose disease in animals |
What are some examples of Schedule I (C-I) drugs? | heroin, LSD, marijuana |
What are some examples of Schedule II (C-II) drugs? | cocaine, morphine, amphetamines, codeine |
What are some examples of Schedule III (C-III) drugs? | hydrocodone, ketamine |