Intro TP

Page 1: Introduction to Pharmacology

  • Overview of pharmacology as a discipline that studies drugs and their effects on the body.

Page 2: Definitions

  • Drug: Any substance that causes a physiological change in the body.

  • Pharmacology: The study of medicine and its effects.

  • Pharmacotherapeutics: The application of drugs to treat diseases and improve health outcomes.

Page 3: Sources of Drugs

  • Plants: Provide various chemicals used in medications.

  • Animals / Humans: Utilize body fluids and glandular secretions.

  • Minerals: Play a role in wound healing.

  • Chemicals: Include synthetic substances created in laboratories.

Page 5: Major Sources of Drugs

  • Plants, Animals, Minerals, Chemicals; with plants being a prominent source.

Page 6: Names of Drugs

  • Chemical Name: Describes the drug's chemical structure.

  • Generic Name: Cheaper imitation of the brand name drug (e.g., ibuprofen).

  • Trade/Brand Name: Market name assigned by pharmaceutical companies (e.g., Motrin).

Page 7: Example of Drug Naming

  • Chemical Name: (RS)-2-(4-(2-methylpropyl)phenyl) propanoic acid

    • Brand Name: Motrin, Advil, Nuprin

    • Generic Name: Ibuprofen

  • Chemical Name: 8-Chloro-1-methyl-6-phenyl-4H-s-triazolo [4,3-α] [1,4] benzodiazepine

    • Brand Name: Xanax

    • Generic Name: Alprazolam

Page 8: Bactroban® Description

  • Brand: Bactroban, a mupirocin ointment for dermatologic use.

  • Composition: Each gram contains 20 mg mupirocin in a polyethylene glycol base.

  • Chemical Name: (E)-(2S,3R,4R,5S)-5-[(2S,3S,4S,5S)-2,3-Epoxy-5-hydroxy-4-methylhexyl)tetrahydro-3,4-dihydroxy-3-methyl-2H-pyran-2-crotonic acid, ester with 9-hydroxynonanoic acid.

Page 10: Cost of Drugs

  • The most expensive drugs to purchase are typically Trade followed by Chemical, then Generic.

Page 11: Types of Drug Therapy

  • Prescription Drugs: Require a doctor's order.

  • BTC (Behind the Counter): Restricted due to potential abuse.

  • Nonprescription Drugs: Available over-the-counter (OTC).

  • Controlled Drugs: Regulated by the DEA (Drug Enforcement Agency).

  • Recreational Drugs: Street drugs that alter the level of consciousness (LOC).

Page 14: Characteristics of an Ideal Drug

  • Effective: Treats a specified condition.

  • Safe: Favorable risk-to-benefit ratio.

  • Selective: Target action in the body.

  • Reversible: Can be reversed with an antidote.

  • Predictable: Known side effects.

  • Free from Interactions: Limited adverse reactions with other drugs.

  • Affordable: Financially accessible.

  • Chemically Stable: Maintains shelf life quality.

Page 15: Sources of Drug Information

  • U.S. Pharmacopeia (USP): Sets drug standards.

  • National Formulary: Drug ingredients reference.

  • PDR (Physician's Desk Reference): Comprehensive drug info.

  • Nursing Drug Handbooks: Provide drug information specific for nursing care.

  • Internet: Verification of credibility required.

  • Pharmaceutical Companies: Offer handouts and resources about drugs.

Page 16: Laws and Legislative Acts in Pharmacology

  • 1906: Pure Food and Drug Act

  • 1938: Food, Drug, and Cosmetic Act

  • 1952: Durham-Humphrey Amendment

  • 1962: Kefauver-Harris Amendment

  • 1970: Controlled Substance Act

  • 1983: Orphan Drug Act

  • 1997: FDA Modernization Act

Page 18: Regulatory Agencies

  • FDA: Regulates medicine and food products.

  • DEA: Monitors controlled substances.

  • CDC: Tracks disease threats.

  • ANA: Advocates for the nursing profession.

  • State Boards of Nursing: Establish standards for nursing practice.

Page 19: Side Effects and ADRs

  • Black Box Warning: Highest level of warning from the FDA.

  • Risks of combining opioids with CNS depressants can lead to severe adverse effects including sedation and respiratory depression.

Page 20: Development of New Drugs

  • Preclinical Research: Laboratory testing prior to human trials.

  • Phase 1: Clinical trials begin with healthy volunteers.

  • Phase 2: Trials performed with patients having the disease.

  • Phase 3: Larger cohort testing.

  • Postmarket Surveillance: Ongoing monitoring for long-term effects.

Page 21: Rights of Medication Administration

  1. Right Patient: Verify name and DOB.

  2. Right Medication: Double-check for look-alikes.

  3. Right Dose: Confirm safe dosage range.

  4. Right Time: Administer based on drug's half-life.

  5. Right Route: Confirm appropriate administration method.

Page 25: Additional Responsibilities in Drug Administration

  • Assessment: Collect relevant data.

  • Documentation: Include name, dose, route, date/time, and patient response.

  • Education: Provide necessary medication information.

  • Evaluation: Determine effectiveness; document refusals with education on risks.

Page 27: Medication Errors Prevention

  • High Alert Medications: Inherent risk involved.

  • Strategies to prevent errors include:

    • Awareness of sound-alike/look-alike medications.

    • Use of Tall Man lettering.

Page 28: The Nursing Process

  • Assessment: Identify patient needs.

  • Diagnosis: Evaluate conditions/needs.

  • Planning: Develop care strategies.

  • Intervention: Execute nursing care plans.

  • Evaluation: Assess outcomes of care.