Pharmacology Flashcards
Highest abuse potential, no accepted medical use. Heroin and LSD.
Schedule I
High abuse potential, written RX w/signature only, no refills. Morphine, codeine alone, amphetamines and oxycodone.
Schedule II
Moderate abuse potential, may phone in, 5 RX in 6 months. Tylenol 3
Schedule III
Lower abuse potential, may phone in, 5 RX in 6 months. Valium (Diazepam) And Darvon.
Schedule IV
Lowest abuse potential, some available OTC. Codeine-containing cough meds (not OTC).
Schedule V
Graph of the relationship between dose of a drug and the response
Log Dose-effect curve
Where the dose is increasing sharply
Therapeutic range
Where the curve plateaus (flattens out)
Maximum response
Amount of drug necessary to produce an effect, it is greater when dose is smaller.
Potency
Maximum response of a drug, regardless of the dose
Efficacy
Time it takes for the drug to have an effect
Onset
Length of time that a drug has an effect
Duration
One measure of duration, amount of time necessary for a drug to fall to 1/2 of its original blood level.
Half life
Placed directly in GI tract, oral route and rectal route.
Enteral
Bypasses the GI tract, IV, IM, SQ, Intradermal, inhalation, topical and sublingual.
Parenteral
Safest, least expensive and most convenient, less predictable blood levels, large area for absorption (small intestine).
Oral route of administration
Occurs when orally-administered drugs initially pass through the hepatic portal circulation (liver), which reduces the amount of effective drug.
First-pass effect
Suppositories, creams, enema. Patient is vomiting, unconscious, poor and irregular absorption rectally.
Rectal route of administration
Most rapid drug response, best for emergency situations, absorption phased bypassed, disadvantages include phlebitis, irretrievability and allergy.
IV (intravascular)
Provides sustained effect, massaging muscle will increase the drugs absorption, Deltoid or gluteal muscles common injection sites.
IM (intramuscular)
Used to administer protein products, insulin is administered subcutaneously-it is activated by GI acid/enzymes, local anesthesia in dentistry is delivered this way, side effects include sterile abscess or hematoma
Subcutaneous
Injection into epidermis, example is tuberculin skin test
Intradermal
Rapid delivery across large surface area of respiratory mucosa. Includes inhalers and nitrous oxide/oxygen.
Inhalation
Applied to body surface (skin, mucosa), most effective in non-keratinized areas, require an increased concentration of the drug, contraindicated in ulcerated burned or abraded surfaces.
Topical
Study how a drug enters the body, circulates in the body, and leaves the body.
Pharmacokinetics
Transfer of a drug from the site of administration to the blood stream.
Absorption
What is most important for absorption of oral drugs?
Small intestine
Process by which a drug leaves the blood stream and enters the body systems.
Distribution
What step does IV administered drugs bypass?
Absorption
Where are drugs distributed?
To organs with highest blood flow
Breaking down of a drug for its removal from the body, also known as biotransformation.
Metabolism
What is the most important site for metabolism of drugs?
Liver
Removal of the drug from the body, terminates drug affects.
Elimination
What is the most important organ for elimination?
Kidneys
Dose-related reaction
Side effects
Occurs when the desired effect is excessive, dose-related
Toxic effects
Hypersensitivity response to a drug, NOT dose related
Allergy
Causal relationship between the drug use of a mother and congenital abnormalities.
Teratogenic effect
Functions without conscious effort.
Autonomic nervous system
“Fight or flight” Increase BP thru vasoconstriction Increase HR Dilates bronchioles and pupils Reduce saliva flow Adrenergic drugs (sympathomimetics) Preganglionic: acetylcholine Postganglionic: norepinephrine
Sympathetic (SANS)
“Rest and digest” Increased blood flow to digestive organs Accelerated peristalsis Constricts bronchioles and pupils Increase saliva Pre and postganglionic: acetylcholine Cholinergic drugs (parasympathomimetics)
Parasympathetic (PANS)
Effects mimic the sympathetic nervous system. Should be avoided with angina, uncontrolled HTN and hyperthyroidism.
Adrenergic Drugs
What are the adverse effects of adrenergic drugs?
CNS(anxiety, fear, tremor, headache)
Cardiac arrhythmia
Hypertension
Xerostomia
Examples of Adrenergic Drugs.
Epinephrine (treats anaphylactic reaction, in local anesthetic as vasoconstrictor, to stimulate heart muscle)
Dopamine (treats shock, low BP and Parkinson’s)
Examples of Adrenergic-blocking Drugs?
Inderal (propranolol): non-selective bets blocker to treat HTN
Tenormin (atenolol): selective beta-blocker to treat HTN
Lopressor (metoprolol): selective beta-blocker to treat HTN
Timoptic (timolol): treat glaucoma
Effects mimic parasympathetic nervous system, contraindicated with asthma, ulcers and cardiac disease.
Cholinergic Drugs
Examples of Cholinergic Drugs?
Pilocarpine used to increase saliva flow in patient’s with Sjogren’s syndrome and can treat glaucoma.
These block the parasympathetic nervous system. Adverse reactions include blurred vision, bladder retention, constipation and dry mouth.
Anticholinergic Drugs
Examples of anticholinergic Drugs.
Atropine: decreases saliva for dental procedures
Imodium: treat diarrhea
Scopolamine: treat motion sickness
Dramamine: treat motion sickness
Nonopioid, mechanism of action is inhibition of prostaglandin synthesis. It is an analgesic, antipyretic, anti-inflammatory, and anti-platelet.
Aspirin
What are the adverse effects of aspirin?
Interferes with clotting, contraindicated with Coumadin (warfarin), GI irritation, hypersensitivity, association with Reye’s syndrome, and tinnitus
Nonopioid, NSAID, Motrin, Advil, mechanism of action is inhibition of prostaglandin synthesis. It is an analgesic, antipyretic and anti-inflammatory. Contraindicated with gastric ulcers, decrease effect of many drugs, and interferes with clotting.
Ibuprofen