Pharm Chapters 1-4 Flashcards
Pharmacology (Pharmacotherapeutics)
area of pharmacy that refers to use of specific drugs to prevent, treat, and diagnose disease
Pharmacokinetics
study of how body deals with the drug in terms of ADME
ADME
absorption, distribution, metabolism, excretion
Pharmacodynamics
what drug does in body including its excretion
Types of Drug nomenclature
Chemical Name
Generic Name
Brand Name
Chemical Name
Organic Chemistry Name
Generic name
like acetaminophen
Brand name
like “Tylenol”
FDA Therapeutic Equivalency Standards
Drug products are considered to be therapeutic equivalents only if they are pharmaceutical equivalents and if they can be expected to have the same clinical effect and safety profile when administered to patients under the conditions specified in the labeling.
Preclinical Testing
Animal trials for safety and efficacy
Human Studies Phase 1
safe dose, effect, kinetics (mostly tested on rats)
Human Studies Phase 2
effectiveness in disorder
Human Studies Phase 3
large scale safety and efficacy (used to determine safe dosages)
- phase where papers to FDA for drug approval are submitted and rejected/accepted
- highly controlled patient studies conducted (minimal medical conditions and other currently taken meds present - potentially poses future problems)
Human Studies Phase 4
post marketing (approved by FDA, but still need to keep track for 3 years minimum of how the general public responds to the drug) **this is where hc community really finds out if drug is safe or not
OTC (over the counter) vs Prescription Medications
OTCs are safe for use by the general population without guidance of a health professional
Prescription meds are for those that have seen a Dr. first, not always safe for the general population
Classes of controlled substances
C1- are illegal (like LSD and cocaine= the good stuff)
C2- major pain meds, like morphine
C3- hydrocodone
C4
C5
**The Lower the class, the higher the potential for abuse
Threshold Effect
the start of efficacy