Pharmacology Flashcards
QD
once/day
BID
twice/day
TID
Three times/day
QID
4 times/ day
PC
After meals
AC
before meals
PO
by mouth
PRN
as needed
HS
at bedtime
Brand Name
manufactures name - first letter capitalized
Generic Name
chemical makeup of drug; all letters lowercase
Enteral Administration
uses GI tract
safest, slowest, most variable route
can be sublingual, oral, or rectal
sublingual and rectal administration avoid first pass effect
Parenteral Administration
by-pass GI tract
IV ⇒ most rapid, complete absorption
IM ⇒ high blood volume
Subcutaneous ⇒ under skin
Intradermal ⇒ in dermis
Topical ⇒ absorbed by capillaries under skin
Inhalation ⇒ nitrous, albuterol
Pharmacokinetics
(Absorption)
entry of the therapeutic agent into bloodstream
depends on: food, pH, route, solubility
IV drugs skip this step
Pharmacokinetics
(Distribution)
from bloodstream to body
oral - liver
sublingual - heart
Bioavailability
x amount of drug will be available after administration to produce a biologic effect
Pharmacokinetics
(Metabolism)
breakdown of drugs for excretion
primary site is the liver
Pharmacokinetics
(Excretion)
removal of drug from body
Primary site is kidney
drug excretion occurs through urine/respiratory system
Glomerulus in nephrons filter blood and produce urine
Sympathetic Nervous System
“Fight or Flight”
Norepinephrine and epinephrine mediate response at the adrenergic receptors
Drugs contraindicated for angina, uncontrolled hypertension, uncontrolled hyperthyroidism
Parasympathetic Nervous System
“rest and digest”
acetylcholine mediates response at cholinergic response
Drugs contraindicated for asthma
Allergic Effects
Unpredictable, not dose related
Type 1 - intermediate
Type 2 - slowest
Therapeutic Index
determines safety of a drug
LD50/ED50
Therapeutic Action
desired result
Therapeutic Range
range between dose-causing minimum effect and
dose-causing minimum adverse effect