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
Potency
amount needed to achieve desired effect
Efficacy
maximum response attained
(highest point on graph is greatest efficacy)
Diuretics
“water pills”
- blocks sodium reuptake in kidneys
- more water is excreted
- first line hypertensive agent
- thiazide or loop diuretic
- side effects ⇒ xerostomia, orthostatic hypotension
Beta-Adrenergic Blockers
decreases BP by decreasing cardiac output
- Beta 1: increase heart muscle contraction
- Beta 2: relax bronchial smooth muscle
Starts with B, E, A, or M
Ends in -olol
Calcium Channel Blockers
inhibit calcium (regulates muscle contractions)
- systemic vasodilation decreases BP
- side effects ⇒ xerostomia, gingival enlargement
- ends in -pine
Angiotensin Converting Enzyme (ACE) Inhibitors
blocks angiotensin II, causing vasodilation
side effects ⇒ dry cough, altered taste, orthostatic hypotension
ends in -pril
Anti-Hypertensive Drug Classes
diuretics
ACE Inhibitors
beta-blockers
Calcium channel blockers
Anti-Bacterial Agents
Penicillin: most commonly prescribed, safe with pregnancy, anaphylaxis is common
Tetracycline: bacteriostatic, concentrates in GCF
Cephalosporin: similar action to penicillin
Clindamycin: premedication in penicillin allergy, GI effects
Metronidazole: treats periodontal infections and ANUG, *avoid alcohol
Anti-Viral Agents
Herpes tx: Acyclovir, Docosanol, Valtrex
HIV/AIDS: AZT, Retrovir
Anti-Fungal Agents
occurs more in immunocompromised pt’s
Nystatin: topical or oral administration, 5ml QID for 2 weeks
Fluconazole: administered orally