pharmacy 1

Proper Utilization of PDR and Drug Handbook

  • PDR (Physician's Desk Reference): A comprehensive resource intended for healthcare professionals, particularly for safe medication practices.

    • Contains drug listings including:

    • Chemical name

    • Brand name(s) (trade name)

    • Generic name

    • Properties

    • Indications

    • Side effects

    • Contraindications

    • Dosages

    • Visual representations of medications

    • Can be obtained from libraries or bookstores and may be provided to physicians free of charge.

Key Terms

  • Allergy: An adverse immune response to a substance that can cause symptoms such as hives, dyspnea, or wheezing.

  • Anaphylaxis: A severe, potentially life-threatening allergic reaction that requires immediate medical attention.

  • Antagonism: A drug interaction where one drug decreases the effect of another drug.

  • Chemical Name: The scientific name that identifies the chemical composition of a drug.

  • Contraindications: Specific situations or conditions that indicate the use of a drug could be harmful.

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

  • Generic Name: The non-proprietary name given to a drug that is usually lower-cased and indicates its chemical makeup.

  • Interactions: The ways in which two or more drugs can affect each other's effects in the body.

  • Pharmacodynamics: The study of the physiological effects of drugs on the body.

  • Pharmacokinetics: The study of how drugs are absorbed, distributed, metabolized, and excreted in the body.

  • Pharmacology: The scientific study of drugs, including their properties and effects.

  • Potentiation: An interaction wherein one drug increases the effectiveness of another.

  • Side Effect: A secondary effect of a medication that may be undesirable but is often expected.

  • Synergism: An interaction wherein two drugs work together to produce an enhanced effect.

  • Trade Name: The brand name under which a drug is marketed and sold.

Understanding Drug Nomenclature

  • Drug Naming Conventions: Each drug has three distinct names:

    1. Chemical Name:

    • E.g., 7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one

    1. Trade Name: (Registered trademark)

    • E.g., Valium

    1. Generic Name:

    • E.g., Diazepam

  • Commercial Aspects:

    • Trade names are registered with the U.S. Patent Office and can only be used by the original manufacturer until the patent expires.

    • After expiration, other companies can produce generic equivalents, which will generally use lowercase letters.

Classification of Drugs

  • Drug Classes: Drugs can be classified by their therapeutic effects and their mechanisms of action.

    • Examples:

    • Adrenergic blocking agents

    • Analgesics

    • Antibiotics

    • Anticoagulants

    • Sedatives

  • Therapeutic Classification:

    • Describes the intended purpose of the drug (e.g., cardiotonic, antiarrhythmic).

Legal Regulations in Pharmacology

  • FDA Regulations:

    • Enacted to protect consumers and ensure drug safety.

    • Key Acts:

    • 1906 Pure Food and Drug Act: Initial regulatory framework.

    • 1938 Federal Food, Drug, and Cosmetic Act: Required safety testing before public distribution.

    • 1952 Durham-Humphrey Amendment: Established prescription requirements for certain drugs.

    • 1962 Kefauver-Harris Amendment: Mandated efficacy testing for medications.

  • Controlled Substances Act (1970):

    • Regulates manufacturing and distribution of drugs prone to abuse and dependency.

    • Controlled substances categorized into schedules (I-V) based on potential for abuse:

    • Schedule I: No accepted medical use and high potential for abuse.

    • Schedule II: High potential for abuse with accepted medical use, strict prescription rules.

    • Schedule V: Lower potential for abuse, can be refilled up to five times in six months.

Pharmacodynamics

  • Definition: The study of how drugs interact with the body.

    • All drugs lead to chemical and physiological changes.

    • Types of Effects:

    • Local Effects: Limited to the area where applied (e.g., topical ointments).

    • Systemic Effects: Effects throughout the body, absorbed into the bloodstream and distributed (e.g., antibiotics).

  • Factors Influencing Drug Action:

    • Age: Elderly may metabolize medications slower; children may respond more sharply.

    • Weight: Dosages often adjusted according to weight.

    • Sex: Hormonal levels and body composition may result in varying reactions to drugs.

    • Health Conditions: Diseases may alter drug metabolism and effects.

    • Tolerance: Extended use of drugs may require higher doses due to decreased effectiveness over time.

Pharmacokinetics

  • Definition: Studies the movement of drugs within the body including:

    1. Absorption: How the drug enters the bloodstream.

    2. Distribution: Movement from blood to tissues.

    3. Metabolism: The breakdown of drugs, typically by the liver.

    4. Excretion: Removal of drugs (or their byproducts) from the body, primarily through the kidneys.

  • Implications: Monitoring is crucial especially in patients with liver or kidney dysfunctions to avoid toxicity.

Drug Actions and Interactions

  • Food-Drug Interactions: Certain medications are best absorbed on an empty stomach while others require food to mitigate side effects.

    • Example:

    • Ampicillin needs to be taken on an empty stomach.

    • Ibuprofen should be taken with food.

  • Drug Interactions: Risk of interactions that can enhance or diminish drug effects, including:

    • Synergism: Combined effect is greater than individual effects.

    • Antagonism: Drug effects diminish when given together.

    • Potentiation: One drug prolongs or exaggerates the effect of another drug.

Side Effects and Allergies in Drug Administration

  • Distinguishing Allergies from Side Effects:

    • Drug Allergy: Life-threatening responses requiring immediate attention; documented clearly in patient records.

    • Side Effects: Expected reactions that might occur, generally not life-threatening (e.g., drowsiness).

  • Monitoring Patient Reactions: Patients should wait in-office post-injection or medication administration to monitor for allergic reactions.

Sources of Information for Drug Safety

  • Utilize reliable resources for up-to-date drug information, including:

    1. PDR

    2. USPDI (U.S. Pharmacopeia Dispensing Information)

    3. AHFS (American Hospital Formulary Service)

    4. Compendium of Drug Therapy

  • These resources provide vital information on drug properties, contraindications, and appropriate usage for healthcare providers.

Prescribing Medications

  • Types of Medication Orders:

    • Administered in-office

    • Dispensed for future use

    • Prescribed with appropriate protocols

  • Instructions for Writing a Prescription:

    • Must include physician's signature, patient's details, medication name, dosage, and instructions.

    • Important to document prescriptions in patient records to maintain legal integrity.

  • Refilling Prescription Protocol:

    • Standard procedure generally requires a patient appointment for controlled substances.

    • Emergency refills require physician verification before calling into pharmacies.