Prescription writing
Chapter 1: Introduction to Prescription Writing
Regulations:
Republic Act 2382: Only physicians authorized to prescribe medicines, includes dentists.
Republic Act 5921: Only registered pharmacies can dispense and sell medications.
Purpose of Prescription:
Acts as a safeguard for patients against unsafe drugs or incorrect medications.
Defined as a written order instructing pharmacists to prepare or dispense specific medication.
Etymology of Prescription:
Derived from Latin prescriptus (to write) - combining prae (before) and scribere (to write).
Historical complexity of prescriptions required a universal language, historically Latin.
Modern Prescriptions:
Currently predominantly in English, though some Latin terms still used.
Legal Requirements for Prescriptions:
Must contain specific elements: prescriber’s and patient’s information, date.
Professional presentation enhances clarity; preprinted prescriptions are more legible than handwritten ones.
Chapter 2: Instructions to Patients
Elements of a Prescription:
Prescriber Information: Name, address, and contact info necessary for follow-up.
Patient Information: Name, age, sex, and address important for legal records and patient care.
Date: Essential for tracking treatment timelines.
Components of a Prescription:
Rx (Superscription): Means "take thou"; directs the patient on taking medication.
Inscription: Contains main details like drug name, strength, dosage, and directions for use.
Subscription: Instructions to the pharmacist on dispensing.
Signatura (Sig): Directions meant for the patient, typically written clearly and concisely.
Concerns with Directions:
Avoid phrases like "as needed" to prevent patient misuse and potential lawsuits.
Chapter 3: Signature of Patient
Importance of Clear Directions:
Ensure patients clearly understand medication usage; avoid ambiguity to prevent overdosing.
Sig signifies importance and clarity in medication administration.
Special instructions may also be indicated for pharmacists.
Chapter 4: Use of Drugs
Rational Use of Drugs:
Ensures prescribed drugs are both effective and affordable.
Key Factors:
Understand patient's problem and collect detailed history.
Formulate a pertinent diagnosis to guide prescription.
Set clear therapeutic objectives for treatment.
Selection of Drug Treatment:
Evaluate available treatment options based on efficacy, safety, suitability, cost, and ease of administration.
Chapter 5: Forms of Drug
Drug Dosage Forms:
Classified based on physical form (solid, liquid), or route of administration (oral, parenteral).
Discusses the importance of updating knowledge on drug developments post-graduation.
Patient Information:
Clearly communicate drug benefits and potential side effects.
Rational Prescribing:
Empirical and systematic medication selection tailored to patient specifics, avoiding personal biases or external pressures.
Chapter 6: Conclusion
Relevant Laws and Regulations:
Republic Act 3720 (Food, Drug, and Cosmetic Act): Ensures quality standards for products.
Generics Act of 1988: Mandates generic identification of drugs by active ingredients.
Republic Act 9165 (Comprehensive Dangerous Drugs Act): Protects citizens from illegal drugs.
RA 9711: Strengthens regulatory capabilities of BFAD regarding food and drugs.
Cheaper Medicines Act of 2008: Ensures accessibility to affordable quality medications.
Best Practices in Prescription:
Avoid leaving blank spaces on prescription pads to prevent fraud.
Maintain professionalism and ensure proper documentation.
Final Note: Importance of continuously educating oneself on pharmaceutical practices and regulations.