SECOND EXAM REVIEW (CH. 10) Flashcards
(86 cards)
the scientific study of how various substances interact with or alter the function of living organisms.
Pharmacology
organization that approves new medications and removes unsafe medications from use
FDA
The United States has a comprehensive system of medication and drug regulation
The Food, Drug, and Cosmetic Act (1938)
- A purpose not approved by the FDA
- At doses different from the recommended doses
- By a route of administration not approved by the FDA
off-label
Classifies certain medications with the potential of abuse into five categories (schedules)
Controlled Substances Act of 1970
Schedule I drugs
heroin, marijuana, LSD
Schedule II drugs
fentanyl (Sublimaze), methylphenidate (Ritalin) cocaine
Schedule III drugs
Hydrocodone (Vicodin), acetaminophen with codeine, ketamine
Schedule IV drugs
Diazepam (Valium), lorazepam (Ativan)
Schedule V drugs
Narcotic cough medicines
heroin, marijuana, LSD
Schedule I drugs
fentanyl (Sublimaze), methylphenidate (Ritalin) cocaine
Schedule II drugs
Hydrocodone (Vicodin), acetaminophen with codeine, ketamine
Schedule III drugs
Diazepam (Valium), lorazepam (Ativan)
Schedule IV drugs
Narcotic cough medicines
Schedule V drugs
what are schedule I drugs?
high abuse potential with no recognized medical purpose
what are schedule II drugs?
high abuse potential with a legitimate medical purpose
Made completely in a laboratory
Synthetic
Made from chemicals derived from plant, animal, or mineral
Semisynthetic
What variables do pharmaceutical companies control?
Concentration
Purity
Preservatives
Other ingredients
medication name used during development
chemical name
medication name used to promote consistency and avoids duplication
nonproprietary name
medication name selected for marketing
brand name
Unites States Pharmacopeia-National Formulary (USP-NF)
Physicians’ Desk Reference (PDR) are sources that provides this type of medical profile
medication monograph