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Overview of Pharmacology
Overview of Pharmacology
PNUR 1104 Online Pharmacology for Health Professionals
Objectives
Define selected key pharmacological terms Identify common sources of drugs Discuss how drugs are classified Differentiate between chemical, generic, and trade names of drugs Identify sources of drug information
Objectives
Summarize the standards and laws which govern drug use. Discuss the categories of controlled substances. Discuss the role of the Food and Drug Administration.
Definition of Terms
Pharmacology Drug Drug therapy Medication Local effects Systemic effects Prototype Drug classification Therapeutic classification Pharmacologic or chemical classification Chemical name Generic name
Definition of Terms
Trade or brand name Bioequivalent Prescription drugs Non-prescription or over-the-counter (OTC) drugs Controlled substances
Sources of Drugs
Historically derived from plants Synthetic drugs manufactured in labs Semisynthetic drugs are naturally occurring substances that have been chemically altered. Biotechnology ( recombinant deoxyribonucleic acid technology)
Drug Classification
Similar drugs are grouped together for purpose of study & for ease of prescribing. Drugs are classified according to their effects on particular body systems, their therapeutic uses & their chemical characteristics.
Drug Classification
Pharmacologic classification Therapeutic classification Chemical classification Other classifications: Body system, General use, Family, Primary action, and indication.
Drug Classification
Example: Morphine is a CNS depressant, narcotic analgesic & opiate as well as the prototype of narcotic analgesics.
Uses of Drugs
Therapeutic uses Palliative uses Prophylactic uses Diagnostic uses Replacement uses
Drug Nomenclature
Chemical name
Generic or nonproprietary name Trade (Brand) or proprietary name
Testing Process
Begins with animal studies reviewed by the FDA for approval to go to next step. Next is clinical trials in humans:
Phase I, Phase II, Phase III, Phase IV (FDA evaluates data) Double-blind, placebo controlled, crossover studies, control studies and subject matching
Cellular physiology
Because all body functions, disease processes, and most drug interactions take place at the cellular level, we must understand cellular physiology.
Cellular physiology
Each body cell has the capacity to function and respond to injury. Although cells differ in various tissues according to location & function, they have common characteristics:
Exchange materials with their environment Communicate with each other
Questions?
Objectives
Identify factors that decrease absorption of an oral drug. Identify mechanisms of drug movement in the body. Discuss absorption, distribution, metabolism, and excretion of drugs in the body.
Objectives
Discuss the main elements of the receptor theory of drug action. Discuss variables that effect drug actions in the body. Identify adverse effects of drugs on the body.
Definition of Terms
Pharmacotherapeutics Pharmacokinetics Passive diffusion Facilitated diffusion Active transport Absorption Distribution
Metabolism Excretion Serum half-life Pharmacodynamics Dose Dosage Toxic dose
Definition of Terms
Lethal dose Route of administration Drug-diet interaction drug-drug interaction Additive effects Synergism Interference Displacement Agonist Antagonist Pharmacogenetics Pharmacoanthropology
Definition of Terms
Adverse effects or side effects Therapeutic effects Toxic effects Hepatotoxicity Nephrotoxicity Ototoxicity Hypersensitivity or allergic reaction Drug fever Idiosyncrasy Anaphylactic reaction Drug dependence
Definition of Terms
Carcinogenicity Teratogenicity Tolerance Cross tolerance Metabolite Drug action Onset of action Peak of action Duration of action Therapeutic blood level Peak blood level Toxic blood level Indication(s) Contraindications
Definition of Terms
Precautions Incompatibility Loading dose Maintenance dose Cumulative effects
Pharmacokinetics
Absorption:
Dosage form Route of administration GI function Increased gastric emptying Food in the stomach SQ or IM injections IV therapy Skin absorption Mucous membrane Lungs
Pharmacokinetics
Distribution: involves the transport of drug molecules within the body.
Carried to sites of action, metabolism & excretion Depends largely on adequacy of circulation Protein binding Only free or unbound portion of drug acts on body cells
Drug distribution in CNS is unique Drug distribution during pregnancy & lactation is unique
Pharmacokinetics
Metabolism: method by which drugs are inactivated or biotransformed by the body.
Changed into one or more inactive metabolites & excreted Kidney can only excrete water soluble substances Most drugs are metabolized by enzymes in the liver
Pharmacokinetics
Metabolism:
Enzyme induction Enzyme inhibition Rate of metabolism Oral drugs absorbed in the GI tract that are extensively metabolized in the liver reduce systemic circulation
Pharmacokinetics
Excretion: refers to elimination of a drug from the body.
Requires adequate functioning of the circulatory system & organs of excretion Most drugs are excreted by the kidneys
Bile Feces Lungs Skin
Pharmacokinetics
Serum half-life: also called elimination half-time, is the time required for the serum concentration of a drug to decrease by 50%. Determined primarily by drugs rates of metabolism & excretion
Short half life require more frequent administration 4-5 half lives are required to achieve steadystate concentrations Eliminated gradually over several half-lives
Pharmacodynamics
Receptor theory of drug action
Specific receptors: enzymes, proteins, nucleic acids Changes in cellular metabolism Changes permeability of cell membrane Modifies physiologic process of cell Receptors vary in type, location & number
Pharmacodynamics
When drug molecules chemically bind with cell receptors, pharmacologic effects are agonism or antagonism:
Agonists Antagonists
Pharmacodynamics
Nonreceptor drug actions: relatively few drugs act by other mechanisms.
Antacids Osmotic diuretics Structurally similar to nutrients Metal chelating agents
Drug-Drug Interactions
Additive effects Synergism or potentiation Interference Displacement Specific antidote Decreased intestinal absorption due to binding activation of enzymes Increased excretion
AGE
Children Pregnancy Newborns Older infants 1 -12 year olds After age 12 Older adults (65 & over)
Body Weight
Larger than average person requires more than average person. Nurse may have to calculate by mg per kg of weight. Fat cells may store drug and release later.
Gender
Altered responses to drugs have been demonstrated possibly due to hormonal influence.
Pathologic Conditions
Disorders may cause an alteration in the pharmacokinetic process:
Hypotension, shock, low plasma Vomiting, diarrhea, malabsorption Liver or kidney disease Malnutrition
Psychological Considerations
Placebo response Attitude and expectations Compliance
Questions?
Objectives
Discuss general principles of drug therapy. Identify information to be included in a medication history. Identify the Food and Drug Administration Pregnancy Categories for drugs.
Introduction
Drug therapy is one of the many nursing responsibilities in client care. To fulfill this responsibility the nurse must be:
Be knowledgeable about pharmacology Monitor responses to drug therapy Teach clients and families about drugs
Drug therapy is guided by childs age, weight, and level of growth and development. Choices of drug is often restricted. Safe therapeutic dosage ranges are less well defined for children. Use the oral route of administration when possible. Use thigh muscle for IM injections. Child-proof containers.
Physiologic age (organ function) is more important than chronological age. S&S attributed to age may be caused by drug therapy. Medications should be taken only when necessary. Review current meds before prescribing new medications.
Questions?