100908 Gen Pharm History (pt1) 1801KB
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Transcript 100908 Gen Pharm History (pt1) 1801KB
GENERAL
PHARMACOLOGY
Better living through pharmacology, pharmokinetics,
and pharmodynamics,
P. Andrews
CAREFUL AND JUDICIOUS USE OF
MEDICATIONS CAN TRULY MAKE A
DIFFERENCE
Things to know
about drugs
Pharmokinetics
Pharmodynamics
Generic names
Trade names
Schedules of drugs
FDA approval process
The Harrison Narcotic
act of 1914
Enteral drug
administration
Parenteral drug
administration
Mechanism of action
Route of
administration
Pure food and drug act
of 1906
Things to
know, cont.
The Federal Food,
Drug and Cosmetic act
of 1938
The DurhamHumphrey
Amendments to the
1938 Act
The Controlled
Substance Act of 1970
OTC medications
Absorption
Six rights of
medication
administration
Bioavailability
Biotransformation
First-pass effect
More things
to know!
Blood-brain barrier
Placental barrier
Oxidation
Hydrolysis
Elimination
Agonist
Antagonist
Agonist-antagonist
Extrapyramidal
symptoms
Idiosyncratic response
Tolerence
Side effect
Cumulative effect
Synergism
Potentiation
Onset of action
Therapeutic index
Half-life
Minimum effective
concentration
Historical trends
Ancient health care
Herbs & minerals - 2,000 BC
Pharmacology by end of Renaissance;
separate from medicine
Vaccinations 1796 (Smallpox)
Insulin, Penicillin early 20th century
Modern health care
Human insulin
tPA
Pharmacology
Chemical name
Precise description chemical composition and
molecular structure
Vecuronium Bromide:
Chemical compound: piperidinum, 1-[(2, 3, 5,
16, 17)-3, 17-bis (acetyloxy)-2-(1piperidinyl)androstan-16yl]-1-methyl-, bromide.
Molecular structure C34H57BrN2O4
Generic name –
Non-proprietary name
FDA approved
First manufacturer
vecuronium bromide
Trade (Proprietary) name
Registered to a specific manufacturer
Marsam Pharmaceuticals, Inc.
Vecuronium
TM
Official name
Assigned by USP
Vecuronium Bromide USP
Drug Sources
Plants
Atropine – Deadly
nightshade plant
Morphine – Opium
plant
Digitalis – Foxglove
Animals and Humans
Insulin
Glucagon
Minerals
Calcium chloride
Sodium
Bicarbonate
Magnesium Sulfate
Synthetics
Bretylium tosylate
Lidocaine
Procainamide
Drug Profiles
Names
Classification
Mechanism of Action
Indications
Pharmacokinetics
Side effects/ adverse reactions
Routes of administration
Contraindications
Dosage
How supplied
Special considerations
Legal stuff
- Federal
Protect the public
Pure Food and Drug Act, 1906
Improve quality and labeling of drugs
Harrison Narcotic Act, 1914
Regulating importation, manufacture, sale, use of
opium, cocaine, derivatives
Federal Food, Drug, Cosmetic Act, 1938
Empowers FDA to enforce, set premarket safety
standards
More Federal stuff
Durham-Humphrey Amendments, 1951
Prescription drug amendments, 1938 act; requires
written or verbal prescription from physician to
dispense some drugs
Created OTC category
Comprehensive Drug Abuse Prevention &
Control Act, 1970 (Controlled substance
act)
Replaces Harrison Narcotic Act
Establishes 5 schedules of drugs
Prohibits refilling of Rx for Schedule II drugs, &
requires original Rx to be filled within 72 hours
Other regulations
Prescription drugs
Designated sufficiently dangerous to require
supervision
OTC
Available in small doses; present low risk
General issues
Drugs must be secured
State laws vary; generally set scope of
practice for EMS
Medical directors can delegate authority to
paramedics
New Drug Development
You Are Responsible!
Know precautions and
contraindications
Practice proper technique
Know how to observe and
document effects
Establish and maintain
professional relationships
with other health care
providers
In disease, all systems are
affected
The three systems can’t exist without each
other
The actions of one impact the actions of the
others
I.e., stress (nervous system) disrupts endocrine
system which may respond with glucocorticoid
production = suppressed immune response
Drug Class Examples
Nitroglycerin
Body system: “Cardiac drug”
Action of the agent: “Anti-anginal”
Mechanism of action: “Vasodilator”
Indications for nitroglycerin
Cardiac chest pain
Pulmonary edema
Hypertensive crisis
Which drug class best describes this drug?
Understand pharmacokinetics,
pharmacodynamics
Have current references available
Take careful drug histories
Evaluate compliance, dosage,
adverse reactions
Consult with medical direction when
appropriate
SIX RIGHTS OF MEDICATION
ADMINISTRATION
Right medication
Right dose
Right time
Right route
Right patient
Right documentation
AND SEVEN – Right to refuse
Cells talk to each other
Three distinct languages
Nervous system
neurotransmitters
Endocrine system
hormones
Immune system
cytokines
Another way to classify drugs
Mechanism of Action
Drugs in each category work on similar sites in the
body and will have similar specific effects/side effects
Example: beta blocker actions and impacts
Suppress the actions of the sympathetic nervous
system
Prehospital administration of epinephrine may not
produce as dramatic effects with a patient taking a
drug in this class
Prehospital example:
Hyperglycemics
Dextrose 50% and glucagon
Both will raise blood glucose
Mechanism of action
Glucagon: hormone that works in the liver to convert
stored chains of carbohydrate to glucose
Dextrose 50%: ready-made simple sugar that is ready
to enter into the cell
Which drug is considered first-line for
hypoglycemia? Why?
What are some limitations for glucagon in the
presence of severe hypoglycemia?
Sources of drug information
On-line - be cautious of source
Pharmacy.com
Medline.com
AMA Drug Evaluation
Physician’s Desk Reference (PDR)
Hospital Formulary
Drug Inserts
Other sources
Controlled
substances
Schedule I. High potential for abuse; no
accepted medical indications
Heroin, LSD, Crack, Marijuana
Schedule II. High potential for abuse, but
have accepted medical indications
Morphine, Fentanyl, meperidine, Dilaudid,
Oxycodone, Cocaine, Codeine, Opium,
Methadone
Schedule III. Less potential for abuse, and
accepted medical indications
Tylenol #3, Vicodin
Schedule IV. Low potential for abuse, but
may cause physical or psychological
dependence.
diazepam, midazolam, butorphanol, lorazepam,
Phenobarbital
Schedule V. Low potential for abuse, but
have small quantities of narcotics
Cough medicine (Vicks 44)
Standardization of Drugs
A necessity
Techniques for measuring a drug’s
strength and purity
Assay
Bioassay
The United States Pharmacopeia
(USP)
Official volumes of drug standards
Medical Control
Medication administration is ALS skill
Medical Director
Actively involved in and ultimately responsible for
all clinical and patient care.
We are extension of physician’s license
Special ConsiderationsPregnant patients
Evaluate benefit vs. risk to fetus
FDA has a scale (A,B,C,D,X) to
indicate drugs that may have
documented problems
Many drugs are unknown to cause
problems
Drugs may cross placental barrier or
through lactation
FDA Pregnancy Categories
A
B
Adequate studies have not
demonstrated a risk to the fetus
Animal studies have not demonstrated a
risk to the fetus; no adequate studies in
humans OR
Adequate studies in pregnant women
have not demonstrated a risk to fetus in
first and last trimester BUT animal
studies show adverse effects
FDA Pregnancy Categories, cont.
C
D
X
Animal studies have demonstrated
adverse effects, but there are no
adequate studies in pregnant woman
Fetal risk has been demonstrated; in
certain circumstances, benefits could
outweigh risks
Fetal risk has been demonstrated. This
risk outweighs any possible benefit to
mother. Avoid using in pregnant
patients.
Special Considerations –
Pediatric patients
Based on weight or BSA
Length-based resuscitation tape
(Broslow’s)
Absorption of oral meds less due to
differences in gastric pH, emptying time,
low enzyme levels
Pediatrics, cont.
Unexpected toxicity common in topically applied
meds
Drugs that bind to protein have higher availability
Neonates have much higher % of extracellular fluid
– may require higher doses
Lower metabolic rate & hepatic system ; higher risk
for toxicity
Figure 6-1 ABroselow tape is useful for calculating drug dosages for pediatric patients.
Special Considerations Geriatric patients
MULTIPLE MEDS A PROBLEM
Physiological effects of aging can lead to altered
pharmacodynamics and pharmacokinetics.
Absorb oral meds slower
Distribution altered
Lipid soluble drugs have greater deposition
Drug action delayed or prolonged
Pharmacology
The study of drugs and their interactions with
the body
Drugs do not confer any new properties on cells
or tissues – only modify or exploit existing
functions
Given for local or systemic action
Pharmacokinetics
The study of the basic processes that
determine duration and intensity of a drug’s
effect
Transport
Active transport
Requires energy to move a substance
ATP ADP
Sodium – potassium pump
Facilitated diffusion
Binds with carrier protein, configuration of cell
membrane changes, allows large molecule to enter
body
I.e., Insulin increases glucose transport from 10-20
fold
Transport, cont
Passive transport
movement of substance without energy
Diffusion
Movement of solute in solvent
Osmosis
Movement of solvent
Filtration
Molecules move across membrane down
pressure gradient
Absorption
IM faster than SC
Enteral administration; must survive digestive
process
Enteric coating; dissolve in duodenum
Many drugs ionize
Ionized drugs don’t absorb across cell membranes
Most drugs reach equilibrium
pH affects ionization
Concentration affects absorption
Loading dose – maintenance dose
Bioavailability
Amount of drug still active after reaching target
tissue
Distribution
Some drugs bind to proteins in blood and
remain for prolonged period
Therapeutic effects due to unbound portion
of drug in blood
Drug bound to plasma proteins can’t cross
membranes
Changing blood pH can affect proteinbinding action of drug.
TCA’s are strongly bound to plasma proteins.