This document provides information about pharmacy internship programs and pharmaceutical dosage forms. It describes minor and major internships in community pharmacy, hospital pharmacy, and manufacturing pharmacy. It also outlines the specific objectives of community pharmacy internships. The document then discusses various pharmaceutical dosage forms including liquids, emulsions, suspensions, gels, and oral solid dosage forms like tablets and capsules. It provides examples of different dosage forms.
This document discusses solutions and provides information on:
- The three types of solutions - solid, liquid, and gaseous solutions depending on whether the solvent is solid, liquid, or gas.
- Factors that affect the rate of solubility such as particle size, agitation, and temperature.
- Factors that affect the solubility of a solute such as temperature, molecular structure, effects of other substances, and pH.
- Examples of oral solutions from different categories such as antidepressants, bronchodilators, antipsychotics, and vitamins.
- Characteristics and preparation methods of aqueous solutions and aromatic waters.
Powders are mixtures of finely divided drugs and chemicals that can be used internally or externally. Powders consist of particles that can range in size from 10 mm to 1 μm. The particle size distribution and properties influence how powders can be used. Before using powders to make pharmaceutical products, their chemical and physical characteristics like morphology, purity, solubility, and stability are analyzed. Proper blending and avoiding segregation of powder mixtures is important for ensuring uniform and consistent dosing.
The document outlines labeling requirements for pharmaceutical products in the Philippines according to Administrative Order No. 55 s. 1988. Key points include:
- The generic name must be the most prominently printed element and enclosed in an outlined box. For products with a brand name, the generic name must be above the brand name and one point size bigger.
- Labels must include the product name, dosage form and strength, category, manufacturer info, net contents, formulation, indications, warnings, batch/lot numbers, and expiration date.
- Specific formatting and font requirements are provided for different label elements and sections. Additional details may be included in package inserts.
- Biological and injectable products have additional labeling elements that
Pharmaceutical dosage forms and drug delivery systemsVIJAY SINGH
This document provides an overview of basic information on pharmaceutical dosage forms and drug delivery systems. It discusses active drug substances and the need for dosage forms to deliver drugs effectively. Common dosage forms are described for oral, rectal, and other systemic routes of administration. These include tablets, capsules, liquids, and suppositories. Immediate and controlled release solid oral dosage forms are also covered. The document aims to familiarize readers with common dosage forms and factors influencing drug delivery through different systems.
The document describes a prescription for Seidlitz powder to treat acute functional constipation in a 30-year-old male patient. Seidlitz powder contains sodium potassium tartarate, sodium bicarbonate, and tartaric acid. It is packaged in two packets - one containing the tartarate and bicarbonate which produces effervescence when mixed with water from the second packet containing tartaric acid. When taken as directed, the powder acts as a saline cathartic to treat constipation.
This document outlines the goals and organization of a hospital pharmacy service. It discusses that the pharmacy service aims to (1) provide qualified pharmacy services to patients and health professionals, (2) assure high quality practice through standards and promotion, (3) promote research, and (4) disseminate pharmaceutical knowledge. It also describes the roles and responsibilities of pharmacy staff, including effective administration, developing patient-oriented clinical services, compounding preparations, providing drug information, participating in research and education, and ensuring quality assurance. The pharmacy is organized under the hospital administration and led by a licensed pharmacist to achieve its objectives through proper management.
This lecture discusses pharmaceutical powders. It begins by defining a pharmaceutical powder as a solid dosage form containing finely divided drugs or chemicals meant for internal or external use. Powders permit drugs to be reduced to a very fine state, enhancing dissolution rate, absorption, and masking unpleasant tastes. The lecture then covers various types of powders including divided powders for internal use (simple, compound, cachet-enclosed), bulk powders (antacids, laxatives), and powders for external use. Methods for reducing particle size like trituration, pulverization, and levigation are also summarized.
Pastes, plasters, and glycerogelatins are semisolid preparations for application to the skin. Pastes contain a high proportion of solids, making them stiff so they remain in place and absorb secretions. Plasters are adhesive masses spread on backing that provide prolonged contact or protection at the application site. Glycerogelatins are plastic masses containing gelatin, glycerin, and medication that are applied while melted and harden on the skin. Examples provided are Lassar's zinc paste and salicylic acid plasters for corns. Preparation methods include mixing or melting components.
This document discusses solutions and provides information on:
- The three types of solutions - solid, liquid, and gaseous solutions depending on whether the solvent is solid, liquid, or gas.
- Factors that affect the rate of solubility such as particle size, agitation, and temperature.
- Factors that affect the solubility of a solute such as temperature, molecular structure, effects of other substances, and pH.
- Examples of oral solutions from different categories such as antidepressants, bronchodilators, antipsychotics, and vitamins.
- Characteristics and preparation methods of aqueous solutions and aromatic waters.
Powders are mixtures of finely divided drugs and chemicals that can be used internally or externally. Powders consist of particles that can range in size from 10 mm to 1 μm. The particle size distribution and properties influence how powders can be used. Before using powders to make pharmaceutical products, their chemical and physical characteristics like morphology, purity, solubility, and stability are analyzed. Proper blending and avoiding segregation of powder mixtures is important for ensuring uniform and consistent dosing.
The document outlines labeling requirements for pharmaceutical products in the Philippines according to Administrative Order No. 55 s. 1988. Key points include:
- The generic name must be the most prominently printed element and enclosed in an outlined box. For products with a brand name, the generic name must be above the brand name and one point size bigger.
- Labels must include the product name, dosage form and strength, category, manufacturer info, net contents, formulation, indications, warnings, batch/lot numbers, and expiration date.
- Specific formatting and font requirements are provided for different label elements and sections. Additional details may be included in package inserts.
- Biological and injectable products have additional labeling elements that
Pharmaceutical dosage forms and drug delivery systemsVIJAY SINGH
This document provides an overview of basic information on pharmaceutical dosage forms and drug delivery systems. It discusses active drug substances and the need for dosage forms to deliver drugs effectively. Common dosage forms are described for oral, rectal, and other systemic routes of administration. These include tablets, capsules, liquids, and suppositories. Immediate and controlled release solid oral dosage forms are also covered. The document aims to familiarize readers with common dosage forms and factors influencing drug delivery through different systems.
The document describes a prescription for Seidlitz powder to treat acute functional constipation in a 30-year-old male patient. Seidlitz powder contains sodium potassium tartarate, sodium bicarbonate, and tartaric acid. It is packaged in two packets - one containing the tartarate and bicarbonate which produces effervescence when mixed with water from the second packet containing tartaric acid. When taken as directed, the powder acts as a saline cathartic to treat constipation.
This document outlines the goals and organization of a hospital pharmacy service. It discusses that the pharmacy service aims to (1) provide qualified pharmacy services to patients and health professionals, (2) assure high quality practice through standards and promotion, (3) promote research, and (4) disseminate pharmaceutical knowledge. It also describes the roles and responsibilities of pharmacy staff, including effective administration, developing patient-oriented clinical services, compounding preparations, providing drug information, participating in research and education, and ensuring quality assurance. The pharmacy is organized under the hospital administration and led by a licensed pharmacist to achieve its objectives through proper management.
This lecture discusses pharmaceutical powders. It begins by defining a pharmaceutical powder as a solid dosage form containing finely divided drugs or chemicals meant for internal or external use. Powders permit drugs to be reduced to a very fine state, enhancing dissolution rate, absorption, and masking unpleasant tastes. The lecture then covers various types of powders including divided powders for internal use (simple, compound, cachet-enclosed), bulk powders (antacids, laxatives), and powders for external use. Methods for reducing particle size like trituration, pulverization, and levigation are also summarized.
Pastes, plasters, and glycerogelatins are semisolid preparations for application to the skin. Pastes contain a high proportion of solids, making them stiff so they remain in place and absorb secretions. Plasters are adhesive masses spread on backing that provide prolonged contact or protection at the application site. Glycerogelatins are plastic masses containing gelatin, glycerin, and medication that are applied while melted and harden on the skin. Examples provided are Lassar's zinc paste and salicylic acid plasters for corns. Preparation methods include mixing or melting components.
This document outlines the requirements for obtaining and renewing a license to operate (LTO) for a drug establishment. It lists 11 documents required for an initial inspection, including documents proving ownership or lease of the establishment, permits, pharmacist qualifications, and standard operating procedures. An additional 13 documents are required for importers, wholesalers, or exporters. Reference materials and standard operating procedures must be presented at inspection. Reissuance of an LTO requires surrender of the original LTO, a picture of the establishment, and proof of renewal fees.
The document outlines the process for generic drug dispensing. A prescription is first evaluated to determine if it is correct, erroneous, or violative/impossible. If correct, the prescription is filled and filed. If erroneous, the prescription is filled but also reported. If violative or impossible, it is not filled but still reported. The customer is then informed of generic alternatives and prices before dispensing their selection.
This document outlines administrative order no. 2014-0034 from the Philippines Department of Health Food and Drug Administration. It establishes rules for licensing drug establishments to ensure compliance with Good Manufacturing Practice, Good Distribution Practice, and other standards. It prescribes the use of electronic submissions and signatures. The order classifies different types of drug establishments and outlines requirements for licensing, variations, renewals, and inspections. It aims to align drug establishment operations with laws and international regulatory standards to ensure safety, efficacy and quality of drugs.
This document provides information on suppositories, including their uses, advantages, challenges, and formulation considerations. Suppositories can be used to deliver drugs locally or systemically when oral administration is not possible. They melt or dissolve at body temperature for drug release and absorption. The document discusses important properties of suppository bases like cocoa butter and synthetic triglycerides, as well as factors that influence drug release and absorption from suppositories. It also provides details on the anatomy and physiology of the rectum relevant to suppository administration.
The document discusses the subdivisions of hospital pharmacy. It begins with introducing hospital pharmacy and its objectives like ensuring availability of right medication. It then describes the various subdivisions like administrative service division, education and training division, in-patient services division, out-patient services division, drug information services division, departmental services division, purchasing and inventory control division, central supply services division, assay and quality control division, manufacturing and packaging division, sterile products division, radiopharmaceutical services division, and intravenous admixture division. Each subdivision is assigned specific responsibilities for efficient functioning of the hospital pharmacy.
Common abbreviations used in the prescriptions by great ngwaziSalum Mkata
The document provides a list of common abbreviations used in medical prescriptions. It includes abbreviations for body parts, directions, frequencies, and forms of medication. It then provides examples of prescription directions to test understanding of the abbreviations. The answers show the translations of mixing instructions, dosages, frequencies, and directions to the patient in plain English. The take home question asks for the instruction to the patient for a prescription of eye drops to be used twice daily.
Pharmaceutical powders are mixtures of finely divided drugs or chemicals meant for internal or external use. Powders have advantages like good chemical stability and ease of swallowing large doses. However, powders also have disadvantages such as the potential for misunderstanding correct usage and difficulty making uniform individually wrapped doses. Proper mixing and particle size reduction are important to ensure homogeneity and the desired properties of pharmaceutical powders.
This document discusses syrups, elixirs, and spirits. It defines syrups as concentrated aqueous preparations for oral use containing sugar, a flavoring agent, and a medicinal agent. Elixirs are clear, sweetened, hydroalcoholic solutions intended for oral use that are usually flavored. Spirits are alcoholic or hydroalcoholic solutions of volatile substances. The document provides details on the classification, components, preparation, storage, and uses of these three types of preparations.
This document discusses different types of liquid pharmaceutical preparations including syrups, elixirs, tinctures, spirits, aromatic waters, liniments, and collodions. It describes the common methods used to prepare these solutions, such as solution with heat, agitation, percolation, and maceration. Key points include that syrups are typically prepared via one of four methods depending on ingredient characteristics, while elixirs are preferred over syrups for maintaining both water-soluble and alcohol-soluble components. Tinctures contain 15-80% alcohol and are prepared from plant or chemical substances. Stability testing ensures formulations meet shelf-life requirements.
This document discusses various types of liquid dosage forms including pharmaceutical solutions, galenicals, decoctions, infusions, percolations, douches, enemas, gargles, washes, juices, sprays, sweeteners, honey, mucilage, jellies, and non-aqueous solutions. Pharmaceutical solutions are homogenous mixtures that can be aqueous or non-aqueous depending on the solubility of the drug. Various extraction and preparation methods are covered for obtaining active ingredients from plants into liquid forms. The uses and formulations of different oral and topical liquid medications are also outlined.
Hi! I made these labels for study purpose. These are not for marketing or something else. i will upload more labels in future.
if you have any trouble downloading these labels. contact me on my email address. Thankyou.
This document provides information about ointments, including their definition, types, bases, preparation, storage, and quality control testing. It defines ointments as greasy semisolid medicated preparations applied topically to the skin. The main types are unmedicated and medicated ointments. Medicated ointments are further divided into dermatologic, ophthalmic, rectal, vaginal, and nasal ointments based on the application site. The five classes of ointment bases are oleaginous, absorption, water-in-oil emulsion, oil-in-water emulsion, and water soluble/miscible bases. Quality control tests evaluate attributes like rate of absorption, irritation potential, and
Capsules can be hard or soft gelatin shells containing medications. Hard capsules have 13-16% moisture and are easier to swallow than soft capsules with over 16% moisture. Capsules offer benefits like precise dosing and packaging but may be difficult for some to swallow. They are manufactured by dipping plates in gelatin solutions to form shells, filling powder or liquid into the shells, and sealing. Quality is ensured through testing size, dissolution, and content uniformity during production.
This document discusses different types of incompatibilities that can occur when mixing ingredients in prescriptions. There are three main types: physical, chemical, and therapeutic incompatibilities. Physical incompatibilities involve a visible change, such as insolubility or immiscibility, resulting in an uneven mixture. Chemical incompatibilities occur via reactions like pH changes that alter the chemical properties. Therapeutic incompatibilities change the intended medical effects. The document provides examples and remedies for each type, such as altering solvents, volumes, or adding emulsifying agents to overcome physical incompatibilities. Care must be taken when mixing ingredients to avoid unwanted interactions.
Prescription and Drug prescription WritingEneutron
This document provides an overview of pharmacology and prescription writing. It defines pharmacology as the study of drugs and their effects on living organisms. Drugs can be natural, synthetic, or semi-synthetic and are classified as either over-the-counter or requiring a prescription. The structure of a prescription includes sections for the doctor's information, instructions to the pharmacist, directions for the patient, and identification of the patient. Prescriptions use standardized abbreviations and symbols to concisely communicate dosing instructions.
This document provides an introduction to the course "Introduction to Pharmaceutics-1" which covers topics like powders and granules, semisolid dosage forms, emulsions, suspensions, and pharmaceutical calculations. The course is worth 3 credits and will be assessed through 2 class assignments worth 60% and an end of semester exam worth 40%. It recommends textbooks and outlines the contents of Unit 1 on powders and granules, including definitions, advantages/disadvantages, preparation methods, types, and uses of powders and granules.
This document provides information about syrups, including their definition, types, components, preparation methods, and packaging. A syrup is defined as a concentrated aqueous preparation of sugar or sugar substitute, which may contain flavorings or medicinal substances. The main types are simple syrups containing only sugar and water, and medicated syrups which also contain therapeutic agents. Syrups are prepared primarily by dissolving ingredients with heat or agitation and commonly contain preservatives for stability. Their packaging involves filling bottles, sealing, labeling, and other processes to ensure safety and extended shelf life.
I. This document discusses different methods of drug distribution in hospitals including individual prescription orders, floor stock systems, unit dose dispensing, and outpatient versus inpatient distribution.
II. The main types of drug distribution systems covered are individual prescription ordering, complete floor stocking, a combination of the two, and unit dose dispensing.
III. Key aspects of each system like advantages, disadvantages, and procedures are summarized.
Dispensing Lab Specialized Drug Delivery Systems And Health Accessoriesdunerafael
This document discusses specialized drug delivery systems and provides advice on their proper use. It defines and illustrates different specialized dosage forms like implants, insufflations, irrigation solutions, and more. Regarding implants, it advises monitoring for pain and avoiding heavy lifting for 24 hours. It recommends inhaling all of the aerosol when using a nebulizer. Allied professionals are advised that only surgeons can implant devices and to watch for swelling and bruising after a procedure.
This document provides an introduction to the field of pharmacology. It defines key terms like pharmacy, pharmacology, drugs, medicines, and drug interactions. It describes how drugs are classified based on origin, chemical structure, means of procurement, body system affected, and mechanism of action. The stages of drug discovery, development and clinical trials are outlined. Philippine laws regarding drug use like the Generics Act and those establishing the Philippine National Drug Formulary are mentioned. Community drug outlets called Botika ng Barangay aimed at improving access to essential medicines are also introduced.
Definition of prescription, Types, Difference between them.
Analyzing some prescriptions and their errors, comparing them with an ideal one.
Methods we should take to minimize those errors.
The document discusses prescriptions and electronic prescribing. It defines a prescription as an order from a medical practitioner for medicine or treatment for a patient. It explains the parts of a prescription including patient information, medication, and instructions. Electronic prescribing allows doctors to transmit prescriptions directly to pharmacies digitally, improving accuracy and reducing errors compared to handwritten prescriptions. While it provides benefits, electronic prescribing also faces challenges such as accidental errors and security issues.
This document outlines the requirements for obtaining and renewing a license to operate (LTO) for a drug establishment. It lists 11 documents required for an initial inspection, including documents proving ownership or lease of the establishment, permits, pharmacist qualifications, and standard operating procedures. An additional 13 documents are required for importers, wholesalers, or exporters. Reference materials and standard operating procedures must be presented at inspection. Reissuance of an LTO requires surrender of the original LTO, a picture of the establishment, and proof of renewal fees.
The document outlines the process for generic drug dispensing. A prescription is first evaluated to determine if it is correct, erroneous, or violative/impossible. If correct, the prescription is filled and filed. If erroneous, the prescription is filled but also reported. If violative or impossible, it is not filled but still reported. The customer is then informed of generic alternatives and prices before dispensing their selection.
This document outlines administrative order no. 2014-0034 from the Philippines Department of Health Food and Drug Administration. It establishes rules for licensing drug establishments to ensure compliance with Good Manufacturing Practice, Good Distribution Practice, and other standards. It prescribes the use of electronic submissions and signatures. The order classifies different types of drug establishments and outlines requirements for licensing, variations, renewals, and inspections. It aims to align drug establishment operations with laws and international regulatory standards to ensure safety, efficacy and quality of drugs.
This document provides information on suppositories, including their uses, advantages, challenges, and formulation considerations. Suppositories can be used to deliver drugs locally or systemically when oral administration is not possible. They melt or dissolve at body temperature for drug release and absorption. The document discusses important properties of suppository bases like cocoa butter and synthetic triglycerides, as well as factors that influence drug release and absorption from suppositories. It also provides details on the anatomy and physiology of the rectum relevant to suppository administration.
The document discusses the subdivisions of hospital pharmacy. It begins with introducing hospital pharmacy and its objectives like ensuring availability of right medication. It then describes the various subdivisions like administrative service division, education and training division, in-patient services division, out-patient services division, drug information services division, departmental services division, purchasing and inventory control division, central supply services division, assay and quality control division, manufacturing and packaging division, sterile products division, radiopharmaceutical services division, and intravenous admixture division. Each subdivision is assigned specific responsibilities for efficient functioning of the hospital pharmacy.
Common abbreviations used in the prescriptions by great ngwaziSalum Mkata
The document provides a list of common abbreviations used in medical prescriptions. It includes abbreviations for body parts, directions, frequencies, and forms of medication. It then provides examples of prescription directions to test understanding of the abbreviations. The answers show the translations of mixing instructions, dosages, frequencies, and directions to the patient in plain English. The take home question asks for the instruction to the patient for a prescription of eye drops to be used twice daily.
Pharmaceutical powders are mixtures of finely divided drugs or chemicals meant for internal or external use. Powders have advantages like good chemical stability and ease of swallowing large doses. However, powders also have disadvantages such as the potential for misunderstanding correct usage and difficulty making uniform individually wrapped doses. Proper mixing and particle size reduction are important to ensure homogeneity and the desired properties of pharmaceutical powders.
This document discusses syrups, elixirs, and spirits. It defines syrups as concentrated aqueous preparations for oral use containing sugar, a flavoring agent, and a medicinal agent. Elixirs are clear, sweetened, hydroalcoholic solutions intended for oral use that are usually flavored. Spirits are alcoholic or hydroalcoholic solutions of volatile substances. The document provides details on the classification, components, preparation, storage, and uses of these three types of preparations.
This document discusses different types of liquid pharmaceutical preparations including syrups, elixirs, tinctures, spirits, aromatic waters, liniments, and collodions. It describes the common methods used to prepare these solutions, such as solution with heat, agitation, percolation, and maceration. Key points include that syrups are typically prepared via one of four methods depending on ingredient characteristics, while elixirs are preferred over syrups for maintaining both water-soluble and alcohol-soluble components. Tinctures contain 15-80% alcohol and are prepared from plant or chemical substances. Stability testing ensures formulations meet shelf-life requirements.
This document discusses various types of liquid dosage forms including pharmaceutical solutions, galenicals, decoctions, infusions, percolations, douches, enemas, gargles, washes, juices, sprays, sweeteners, honey, mucilage, jellies, and non-aqueous solutions. Pharmaceutical solutions are homogenous mixtures that can be aqueous or non-aqueous depending on the solubility of the drug. Various extraction and preparation methods are covered for obtaining active ingredients from plants into liquid forms. The uses and formulations of different oral and topical liquid medications are also outlined.
Hi! I made these labels for study purpose. These are not for marketing or something else. i will upload more labels in future.
if you have any trouble downloading these labels. contact me on my email address. Thankyou.
This document provides information about ointments, including their definition, types, bases, preparation, storage, and quality control testing. It defines ointments as greasy semisolid medicated preparations applied topically to the skin. The main types are unmedicated and medicated ointments. Medicated ointments are further divided into dermatologic, ophthalmic, rectal, vaginal, and nasal ointments based on the application site. The five classes of ointment bases are oleaginous, absorption, water-in-oil emulsion, oil-in-water emulsion, and water soluble/miscible bases. Quality control tests evaluate attributes like rate of absorption, irritation potential, and
Capsules can be hard or soft gelatin shells containing medications. Hard capsules have 13-16% moisture and are easier to swallow than soft capsules with over 16% moisture. Capsules offer benefits like precise dosing and packaging but may be difficult for some to swallow. They are manufactured by dipping plates in gelatin solutions to form shells, filling powder or liquid into the shells, and sealing. Quality is ensured through testing size, dissolution, and content uniformity during production.
This document discusses different types of incompatibilities that can occur when mixing ingredients in prescriptions. There are three main types: physical, chemical, and therapeutic incompatibilities. Physical incompatibilities involve a visible change, such as insolubility or immiscibility, resulting in an uneven mixture. Chemical incompatibilities occur via reactions like pH changes that alter the chemical properties. Therapeutic incompatibilities change the intended medical effects. The document provides examples and remedies for each type, such as altering solvents, volumes, or adding emulsifying agents to overcome physical incompatibilities. Care must be taken when mixing ingredients to avoid unwanted interactions.
Prescription and Drug prescription WritingEneutron
This document provides an overview of pharmacology and prescription writing. It defines pharmacology as the study of drugs and their effects on living organisms. Drugs can be natural, synthetic, or semi-synthetic and are classified as either over-the-counter or requiring a prescription. The structure of a prescription includes sections for the doctor's information, instructions to the pharmacist, directions for the patient, and identification of the patient. Prescriptions use standardized abbreviations and symbols to concisely communicate dosing instructions.
This document provides an introduction to the course "Introduction to Pharmaceutics-1" which covers topics like powders and granules, semisolid dosage forms, emulsions, suspensions, and pharmaceutical calculations. The course is worth 3 credits and will be assessed through 2 class assignments worth 60% and an end of semester exam worth 40%. It recommends textbooks and outlines the contents of Unit 1 on powders and granules, including definitions, advantages/disadvantages, preparation methods, types, and uses of powders and granules.
This document provides information about syrups, including their definition, types, components, preparation methods, and packaging. A syrup is defined as a concentrated aqueous preparation of sugar or sugar substitute, which may contain flavorings or medicinal substances. The main types are simple syrups containing only sugar and water, and medicated syrups which also contain therapeutic agents. Syrups are prepared primarily by dissolving ingredients with heat or agitation and commonly contain preservatives for stability. Their packaging involves filling bottles, sealing, labeling, and other processes to ensure safety and extended shelf life.
I. This document discusses different methods of drug distribution in hospitals including individual prescription orders, floor stock systems, unit dose dispensing, and outpatient versus inpatient distribution.
II. The main types of drug distribution systems covered are individual prescription ordering, complete floor stocking, a combination of the two, and unit dose dispensing.
III. Key aspects of each system like advantages, disadvantages, and procedures are summarized.
Dispensing Lab Specialized Drug Delivery Systems And Health Accessoriesdunerafael
This document discusses specialized drug delivery systems and provides advice on their proper use. It defines and illustrates different specialized dosage forms like implants, insufflations, irrigation solutions, and more. Regarding implants, it advises monitoring for pain and avoiding heavy lifting for 24 hours. It recommends inhaling all of the aerosol when using a nebulizer. Allied professionals are advised that only surgeons can implant devices and to watch for swelling and bruising after a procedure.
This document provides an introduction to the field of pharmacology. It defines key terms like pharmacy, pharmacology, drugs, medicines, and drug interactions. It describes how drugs are classified based on origin, chemical structure, means of procurement, body system affected, and mechanism of action. The stages of drug discovery, development and clinical trials are outlined. Philippine laws regarding drug use like the Generics Act and those establishing the Philippine National Drug Formulary are mentioned. Community drug outlets called Botika ng Barangay aimed at improving access to essential medicines are also introduced.
Definition of prescription, Types, Difference between them.
Analyzing some prescriptions and their errors, comparing them with an ideal one.
Methods we should take to minimize those errors.
The document discusses prescriptions and electronic prescribing. It defines a prescription as an order from a medical practitioner for medicine or treatment for a patient. It explains the parts of a prescription including patient information, medication, and instructions. Electronic prescribing allows doctors to transmit prescriptions directly to pharmacies digitally, improving accuracy and reducing errors compared to handwritten prescriptions. While it provides benefits, electronic prescribing also faces challenges such as accidental errors and security issues.
A prescription is a written order from a physician directing a pharmacist to dispense medication. There are two types: pre-compounded prescriptions for already prepared drugs, and extemporaneous prescriptions where the pharmacist prepares the medication. A prescription should include the date, prescribing doctor's information, patient information, drug name and dosage, directions, and doctor's signature. Abbreviations are commonly used in prescriptions to save space. Rational prescribing fulfills medical criteria while irrational prescribing inappropriately uses drugs.
Reagan Stokes completed a health science internship at the Anderson Free Clinic pharmacy under pharmacist Lisa Thorndyke. As an intern, Reagan assisted with pharmacy tasks like dispensing medications, checking prescription bags, and ordering refills. Reagan also helped with clinic operations such as scanning patient files, making appointments, and transitioning the clinic to an electronic records system. Throughout the internship, Reagan gained valuable experience in pharmacy work and affirmed plans to pursue pharmacy school.
This document summarizes different types of drugs used to treat constipation. It describes bulk forming agents, osmotic agents, stool softeners, and stimulant purgatives. It provides details on specific osmotic laxatives like magnesium sulfate and lactulose, explaining their mechanisms of action, indications, dosages, and side effects. The document warns that long-term use of stimulant laxatives can lead to a condition called cathartic colon.
Prostaglandins are hormone-like lipid compounds that are produced in various tissues and mediate important physiological functions. They were discovered in the 1930s and their chemical structures were elucidated in the 1950s. Sune Bergström, Bengt Samuelsson, and John Vane conducted seminal research in the 1960s and 1970s on prostaglandin biosynthesis, metabolism, and physiological roles. Their work showed that prostaglandins are derived from fatty acids and mediate processes like inflammation and reproduction. Bergström, Samuelsson, and Vane received the 1982 Nobel Prize in Physiology or Medicine for their discoveries concerning prostaglandins.
The document discusses the definition and scope of pharmacy practice. It describes various areas of pharmacy including community pharmacy, hospital pharmacy, clinical pharmacy, nuclear pharmacy, industrial pharmacy, pharmaceutical education, and more. It also discusses prescriptions, providing definitions and describing the typical components of a prescription, including the superscription, inscription, and subscription. The document is intended to provide an orientation to the field of pharmacy.
The document discusses the therapeutic uses of prostaglandins. It describes how prostaglandins are synthesized from arachidonic acid via various pathways, including the cyclooxygenase pathway which generates prostaglandins. Prostaglandins have various effects in the female reproductive system, with PGF2α and PGE2 promoting uterine contractions and cervical ripening, making prostaglandin analogs useful for inducing labor and abortions.
1. Suspensions are two-phase systems consisting of finely divided solid particles dispersed in a liquid vehicle. The document discusses the characteristics of various types of suspensions including oral, topical, ophthalmic, and injectable suspensions.
2. Important characteristics of pharmaceutical suspensions include particle size between 1-50um, use of suspending agents to prevent settling, and viscosity suitable for administration. Commonly used suspending agents are listed.
3. Examples of different categories of oral suspensions are provided such as antacids, antibiotics, antifungals, antihypertensives, and more. The key characteristics and examples of specific types of suspensions like antacid and antibacterial suspensions are also summarized.
Mandatory labelling requirements in the Philippines include providing the product identity or name, net content declaration, list of ingredients, name and address of manufacturer or packer, country of origin, lot identification code, and open-date marking for some foods. Labels must also include the principal display panel showing key information and the information panel listing additional details like ingredients and nutrition facts. Barcodes used on packages follow global standards with country-specific coding to identify the product and manufacturer.
A prescription is a written or verbal order from a licensed medical professional for a medication. Prescriptions have been used since ancient times and Latin was adopted as the standard language. Prescriptions must clearly identify the patient and include details like drug name, dose, frequency, and prescriber information. There are different types of prescriptions for different settings like hospitals, general practice, and private use. Proper prescription writing aims to prevent errors by using unambiguous terminology and formats. Common errors in drug administration must be reported to allow for proper management.
This document discusses dispensing in pharmacy practice. Dispensing involves interpreting prescriptions to supply appropriate medicines to patients. It describes the key activities in dispensing like receiving prescriptions, checking for completeness and legality, filling prescriptions, and providing directions for patients. It emphasizes the importance of a well-organized dispensing environment and carefully checking prescriptions to avoid errors due to illegibility or similar drug names. Dispensers must concentrate to ensure the correct medicines are accurately dispensed.
The document provides an overview of community pharmacy training. It discusses topics such as familiarization with prescriptions, prescription dispensing, procurement of goods, store management, monitoring aids, and the learning process. Specific conditions covered include heart disease, dyslipidemia, and dysmenorrhea. Treatment options are presented for dyslipidemia such as statins, fibrates, and supplements. Analgesics, NSAIDs, antispasmodics, and hormones are discussed as treatment approaches for dysmenorrhea. The training aims to equip pharmacy assistants with knowledge to properly assist patients.
This document provides an overview of the cardiovascular system, including the structure and organization of blood vessels. It describes the two main circuits (pulmonary and systemic), the histological layers of arteries and veins, and the types and organization of arteries, arterioles, capillaries and veins. Diagrams and figures are included to illustrate the structures described. Key points covered are the layers of blood vessels, size ranges of different vessel types, and the flow of blood through the pulmonary and systemic circuits.
This document discusses prostaglandins and leukotrienes, local hormones derived from arachidonic acid that have many functions in the body. It describes their biosynthesis pathways through cyclooxygenase and lipoxygenase enzymes, and the actions of specific prostaglandins and leukotrienes in processes like inflammation, smooth muscle tone, blood coagulation, and reproduction. The document also outlines their roles in conditions like peptic ulcers, glaucoma, erectile dysfunction, and pulmonary issues. Prostaglandin preparations are used for therapeutic abortion, cervical ripening, postpartum hemorrhage, and various ulcer and eye conditions. Side effects can include vomiting, diarrhea, and abdominal cramps.
This document discusses classical dosage forms, which are conventional dosage forms prepared without advanced techniques. It describes various classical dosage forms including syrups, decoctions, elixirs, ointments, and lotions. Syrups are concentrated sugar solutions that can preserve drug components. Decoctions are extracts made by boiling drugs in water. Elixirs are sweetened alcoholic solutions. Ointments are semisolid preparations for external use. Lotions are fluid preparations for external application without friction. Examples of each type are provided along with preparation methods and uses.
This document discusses classical dosage forms, which are conventional dosage forms prepared without advanced techniques. It describes lozenges as medicated candies dissolved in the mouth to soothe throat irritation. Pills are small, round solids containing medication. Cachets enclose medication within a wafer shell. Draughts are single-dose liquid preparations packaged in larger volumes. Suppositories and pessaries are solid medications inserted into orifices to exert local or systemic effects as they dissolve.
The document outlines the key aspects and operations of community pharmacies and hospital pharmacies, including types of community pharmacies, customer service, processing prescriptions, preparing prescriptions, other duties like stocking and ordering, customer pick up processes, and the organization and functions of hospital pharmacies like medication packaging, formularies, and sterile compounding.
The document defines drugs and dosage forms. It explains that dosage forms transform pure drug compounds into predetermined forms mixed with non-drug components to aid drug delivery. Dosage forms provide accurate dosing, protection, masking of taste/odor, and controlled release. There are various types of dosage forms classified by route of administration and physical form including solids, liquids, semi-solids, and gases. Common solid dosage forms are tablets, capsules, powders, and granules while liquids include solutions, emulsions, suspensions, elixirs and linctuses. Semi-solid forms for external use are ointments, creams, pastes and jellies.
This document defines and classifies pharmaceutical dosage forms. It discusses that dosage forms contain active pharmaceutical ingredients and excipients formulated into solid, semi-solid, liquid or gaseous forms for administration. Solid dosage forms are classified as unit (e.g. tablets, capsules) or bulk (e.g. powders). Semi-solid forms include creams, ointments, and gels for topical use. Liquid forms comprise solutions, syrups, elixirs, emulsions and suspensions for oral or other internal use. Gaseous forms like inhalants and aerosols are administered via respiratory routes. Various types of these dosage forms are described based on their formulations and routes of administration.
This document discusses different dosage forms used to deliver drugs to the body. It defines dosage forms as the means of delivering active pharmaceutical ingredients (APIs) to sites of action within the body. Dosage forms contain APIs and excipients. They are classified based on route of administration and physical form. Solid dosage forms include tablets, capsules, and implants. Semi-solid forms include ointments, creams, and suppositories. Liquid forms include oral solutions, suspensions, and emulsions. The document provides examples and descriptions of various common dosage forms.
This presentation provides an overview of different dosage forms including their definitions, classifications, and examples. It discusses solid dosage forms like tablets and capsules, liquid forms like syrups and suspensions, and semisolid forms like ointments and creams. The key points are:
- A dosage form refers to the physical form of a drug, such as a tablet, capsule, or liquid, and how it is administered.
- Dosage forms are classified by their physical form (solid, liquid, semisolid), route of administration (oral, topical, parenteral), and release rate (immediate or sustained release).
- Common solid dosage forms include tablets, capsules, and powders. Liquid
This document summarizes key aspects of liquid dosage forms. It defines liquid dosage forms as solutions or suspensions for oral or injectable administration. It describes various types of liquid formulations including syrups, elixirs, tinctures, and discusses advantages and disadvantages. It also discusses important excipients used in liquid formulations such as vehicles, solubilizers, preservatives, stabilizers and how they impact properties. Finally, it provides examples of specific liquid dosage forms including ear drops, nasal sprays, mouthwashes and their intended use and advantages.
This document discusses various dosage forms used to deliver drug molecules to sites of action within the body. It defines dosage forms and describes their classification based on route of administration and physical form. Several oral dosage forms are described in detail, including tablets, capsules, liquids, and others. Topical, rectal, vaginal, parenteral, inhaled, and other dosage forms are also summarized. The purpose, composition, and examples of each type of dosage form are provided.
This document discusses different types of dosage forms, which are means of delivering drug molecules to sites of action in the body. It describes various oral dosage forms including tablets, capsules, liquids, and others. It also covers topical dosage forms such as ointments, creams, gels, and more. Oral dosage forms provide accurate dosing, protection from gastric acid, and masking of taste, while topical forms are used on the skin or mucous membranes to deliver drugs locally. The document provides details on the composition, use, and advantages of many common dosage forms.
A brief description of pharmaceutical dosage forms and their route of administration and typical process flow and manufacturing details. It may help new aspirants who wnts to knoiw aboute dosageforms and their administration routes.
This document discusses various types of dosage forms including their definitions, classifications, and examples. It covers solid dosage forms like tablets, capsules, and powders as well as liquid forms like solutions, suspensions, and emulsions. It also discusses semi-solid forms like ointments, creams, gels and pastes. Additionally, it covers various routes of administration such as oral, topical, rectal, parenteral, inhaled and others. It provides details on the composition, use and examples of different dosage forms based on their physical properties and intended route of delivery.
This document defines and classifies different types of dosage forms. It discusses oral solid dosage forms like tablets, capsules, granules and powders. It also covers oral liquid forms such as solutions, suspensions, syrups and elixirs. Finally, it summarizes topical dosage forms including ointments, creams, gels, pastes and dusting powders which are applied externally to the skin or mucous membranes. The purpose of different dosage forms is to deliver drug molecules accurately to sites of action in the body while protecting, masking taste and ensuring sustained or controlled release of medication.
The means (or the form) by which drug molecules are delivered to sites of action within the body.
The drugs are rarely administered in their original pure state. They are administered in different dosage forms after converting them into a suitable formulation.
The dosage form is a combination of the drug and different kinds of non-drug compounds called “additives”.
The document discusses the need for dosage forms and summarizes their purposes. Dosage forms are necessary because most drugs are administered in low milligram or microgram quantities that cannot practically be measured or obtained by the general public from bulk materials. Dosage forms also serve to protect drugs, conceal tastes, provide liquid preparations, control drug release rates, enable topical and insertion administration, and allow placement in the body. Before developing a dosage form, the desired product type and goals must be determined to guide formulation. Common dosage forms include solutions, ointments, creams, pastes, gels, jellies, poultices, plasters, suppositories and more.
1. The document discusses different types of dosage forms including solid, liquid, semi-solid, inhaled, and rectal/vaginal dosage forms.
2. Solid dosage forms include tablets, capsules, powders, and granules. Liquid forms include solutions, emulsions, suspensions, syrups and elixirs. Semi-solid forms include ointments, gels, creams and pastes.
3. The document provides examples of each dosage form and explains their composition, use, advantages, and route of administration. The classification of dosage forms is also described based on physical form and route of administration.
The document discusses various dosage forms and drug delivery systems. It begins by defining dosage forms as means of delivering drug molecules to sites of action. It then covers different types of solid, liquid, semi-solid, inhaled, rectal and vaginal dosage forms. Key points include classifications based on route of administration (oral, parenteral, etc.) and physical form (solid, liquid, semi-solid). Common examples are provided for different dosage forms like tablets, capsules, solutions, suspensions, creams, inhalers, and suppositories.
This document describes various types of dosage forms including their definitions, classifications, and examples. It discusses oral dosage forms like tablets, capsules, liquids, and others. It also covers topical forms like ointments, creams, gels and more. Rectal forms like suppositories and enemas are outlined. Vaginal forms such as pessaries and rings are defined. Finally, it briefly discusses parenteral forms including intravenous and intramuscular injections. The document provides detailed information on the characteristics and uses of different dosage forms for drug delivery.
This document discusses different types of dosage forms including oral and topical dosage forms. Oral dosage forms include tablets, capsules, liquids, and others. Tablets can be coated, sublingual, effervescent, chewable and more. Capsules are either hard or soft shelled. Topical dosage forms include ointments, creams, gels, pastes, liniments and others that are applied to the skin or mucous membranes for local effects. Dosage forms are designed to deliver drugs to sites of action in the body in a way that protects, masks tastes, and controls drug release.
This document provides an overview of different dosage forms used to deliver drug molecules to sites of action within the body. It discusses both oral and topical solid and liquid dosage forms such as tablets, capsules, ointments, creams, and more. It also covers parenteral forms like injections as well as inhaled, rectal, and vaginal dosage forms. The document classifies dosage forms based on their physical form and route of administration and provides examples and descriptions of common forms.
This document describes various types of dosage forms including their definitions, classifications, and examples. It discusses oral dosage forms like tablets, capsules, liquids, and others. It also covers topical forms like ointments, creams, gels and more. Rectal forms like suppositories and enemas are outlined. Vaginal forms such as pessaries and rings are defined. Finally, it briefly discusses parenteral forms including intravenous and intramuscular injections. The document provides detailed information on the characteristics and uses of different dosage forms for drug delivery.
This document provides an overview of pharmaceutical dosage forms. It defines a dosage form as the physical form that a drug takes, such as solid, liquid, or gas, to deliver the drug to a particular site in the body. Dosage forms are classified based on route of administration and physical form. The key functions of dosage forms are to protect drugs, improve therapeutic activity, and enhance patient compliance. Various types of solid, liquid, semisolid, and gaseous dosage forms are described along with their characteristics and examples.
Pharmaceutical dosage forms can be classified based on their route of administration, physical form, or both. The main types include oral, topical, parenteral, rectal, vaginal, inhalational, ophthalmic, otic, and nasal dosage forms. Oral dosage forms include liquids such as solutions, suspensions, emulsions, elixirs, and mixtures. They also include solids such as tablets, capsules, powders, and granules. Topical dosage forms include semisolids like ointments, creams, pastes, and jellies. Parenteral dosage forms are sterile preparations meant for injection or infusion.
2. Pharmacy Internship
Minor Internship
Community Pharmacy Internship
4 units
1 unit lecture (1 hour/week)
3 units laboratory (200 hours)
Hospital Pharmacy Internship
4 units
1 unit lecture (1 hour/week)
3 units laboratory (200 hours)
Manufacturing Pharmacy Internship
4 units
1 unit lecture (1 hour/week)
3 units laboratory (200 hours)
Major Internship (any of the 3 areas)
Major Int. 1 (INT4) : 4 units
1 unit lecture (1 hour/week)
3 units laboratory
Major Int. 2 (INT4B) : 4 units
1 unit lecture (1 hour/week)
3 units laboratory
360 HOURS
TOTAL HOURS
OF INTERNSHIP:
960
4. Community Pharmacy Internship
Provides the intern with the unique opportunity of being the
most accessible health professional in the community.
Develops the skills of the interns in dispensing prescriptions,
problem-solving and patient counselling.
Provides an opportunity for the interns to learn the basic
elements in the operation of community pharmacy
5. SPECIFIC OBJECTIVE OF
COMMUNITY PHARMACY INTERNSHIP
1. Acquire proficiency in filling and dispensing prescriptions.
2. Practice effective communication skills in counselling
patients regarding drug administration, storage,
precautions and adverse drug reactions.
3. Practice
7. Dosage Form
also known as pharmaceuticals. It is
define as preparation devised to make
possible administration of medications in
measured or prescribed amount.
8. Terminologies:
• Parenteral Dosage Forms – are preparation introduced
into the body by injection through the skin, the mucous, or
the serous membranes
• Dosage forms for inhalation – are preparations intended
to be finally dispensed or vaporized to the mucous membranes
of the lower part of the respiratory tract.
9. Terminologies:
Oral Dosage Forms - are preparations intended to be taken
orally.
Rectal Dosage Forms - are preparations employed
for systemic effect or a local action through the rectum.
10. Terminologies:
Dosage Forms For Topical application are
preparations intended to be applied on the skin or instilled
into eyes, nose, or ears.
11. LIQUIDS
A. Solutions – a homogenous mixture that is prepared
by dissolving a solid or liquid or gas in another liquid; it
represents a group of preparations in which the molecules of
the solute or dissolved substances are dispersed among those
of the solvent
12. Solutions
Water – used mainly as a vehicle and as a solvent for the
desired flavoring or medicinal ingredients.
Aromatic water – also known as medicated water,
clear saturated aqueous solutions of volatile oils or
aromatic or volatile substances.
Aqueous acids – official inorganic acids and certain
acids although of minor significance as therapeutic
agents are great importance in chemical and
pharmaceutical manufacturing.
13. Solutions
• Diluted acids – aqueous solutions of suitable strength
usually 10% w/v except diluted acetic acid which is 6%
w/v
• Douches – aqueous solutions directed against a part or
into a cavity of the body
• Enemas – also known as evacuation enemas. They
are rectal injections employed to evacuate bowel retention
enemas to influence the general system by
absorption, or to effect locally the seat of disease.
14. Solutions
• Gargles – aqueous solutions used for treating the
pharynx and nasopharynx by forcing air from the
lungs through the gargle which is held in the throat.
• Mouthwashes – aqueous solutions which are most
often used for their deodorant, refreshing, or antiseptic
effect.
• Juices – prepared from fresh ripe fruits, aqueous in
character and used in making syrups which are
employed as vehicles.
15. Solutions
Nasal solutions – usually aqueous solutions which are
deigned to be administered to the nasal passages in
drops or spray form.
Otic solutions – aqueous preparations dispensed in a
container which permits the administration of drops to
the ear
16. NON-AQUEOUS
• Collodion –liquid preparations containing pyroxillin
in a mixture of ethyl ether and ethanol.
• Elixirs – clear, pleasantly flavored sweetened hydro-
alcoholic liquids intended for oral use.
• Glycerites – solutions or mixtures of medicinal
substances in not less than 505 by weight of glycerin
17. NON-AQUEOUS
• Inhalations – are solutions of drugs administered by
the nasal or oral respiratory route for local or
systemic effect.
• Liniments – solutions or mixtures of various substances
in oil, alcoholic solutions of soap or emulsions.
• Oleovitamins – fish liver oils diluted with edible
vegetable oil or solutions of volatile substances of the
indicated vitamins or vitamin concentrates (usually A
and D) in fish liver oil.
18. NON-AQUEOUS
Spirits – known as essences; are alcoholic hydro-alcohol
solutions of volatile substances.
Toothache drops – preparations used for
temporary relief of toothache by application of cotton
saturated with the product into tooth cavity
19. • EMULSION – a two phase system prepared by combining
two immiscible liquids one of which is uniformly dispersed
through the other; they consist of globules that have
diameters equal to or greater than those of the largest
colloidal particles.
• SUSPENSIONS – a two-phase system consisting of finely
divided solid dispersed in a solid, liquid, or gas.
20. GELS – semi-solid systems of either suspension made
up of small inorganic particles or large organic
molecules interpenetrated by a liquid.
LOTIONS – usually liquid suspension or dispersions
intended for external application to the body.
21. MAGMAS and MILK – aqueous suspensions of
insoluble inorganic drugs; they differ from gels
mainly in that the suspended particles are layers.
TINCTURES – alcoholic or hydroalcoholic solutions
prepared from vegetable materials or from chemical
substances
22. FLUIDEXTRACTS – liquid preparation of vegetable
drugs containing alcoholic as a solvent or as
preservative or both, so made that each mL contains
the therapeutic constituents of 1 g of the standard drug
that it represents
EXTRACTS – concentrated preparations of vegetable
or animal drugs obtained by removal of the active
constituents of the respective drugs with suitable
menstruum.
23. PARENTERAL PREPARATION – sterile preparations
intended to be administered by injection under or through one
or more layers of skin or mucous membranes
INTRAVENOUS ADMIXTURES – mixture of intravenous
fluids and drugs to be administered by injection
24. OPHTHALMIC PREPARATIONS – sterile
preparations to be used on the eyes
Solutions – intended for the eye; clear, sterile solution to
be instilled into the eyes by the use of a dropper.
Suspensions – dispersion of finely divided relatively
insoluble drug substances in an aqueous vehicle containing
suitable suspending and dispersing agent.
Ointment – intended for the eyes; they contain medicinal
agents added to the ointment base of white petrolatum and
mineral oil either as a solution or as a micronized powder.
26. MEDICATED
• OINTMENT – semi-solid preparations intended for
external applications to the skin or mucous membranes.
• CATAPLASM – a soft moist mass of meals, herb,
seed usually applied hot in clothes.
• PASTES – concentrates of absorptive powders
dispersed in petrolatum or hydrophilic petrolatum
27. • POWDERS for external use are usually described as
dusting powders, usually contain starch, talc, and zinc
stearate
• DRESSINGS – external applications resembling
ointment usually used as a covering or protection.
• CREAMS – viscous liquid or semi-solid emulsions of
either the oil in water or water in oil type
28. • PLASTERS – substances intended for external
application; they are made of such materials and of
such consistency as to adhere to the skin and attach to a
dressing
• SUPPOSITORIES – solid dosage forms of various
weights and shapes usually medicated for insertion into the
rectum, vagina, or the urethra
29. POWDERS
• Oral powders – generally supplied as finely divided
or effervescent granules
• Dentifrices – may be prepared in the form of a bulk
powders generally containing soap or detergent, mild
abrasive and anticariogenic agent
• Douche powders – soluble powders intended to be
dissolved in water prior to use as antiseptic or cleaning
agents for a body cavity.
30. Dusting powders – locally applied non-toxic
preparations that are intended to have no systemic action.
Insufflations – finely divided powders introduced into
the body cavities.
Triturations –dilutions of potent powdered drugs
prepared by intimately mixing them with a suitable
diluent in 1:10 dilutions
31. ORAL SOLID DOSAGE FORMS
• TABLET – solid dosage form containing drug
substances with or without suitable diluents and prepared
either by compression or molding methods.
• CAPSULES – solid dosage forms in which the drug
substance is enclosed in either a hard or soft soluble
container or of a suitable form of gelatin
• PILLS – small, round, solid dosage forms containing
medicinal agents and intended for oral administration
32. ORAL SOLID DOSAGE FORMS
• TROCHES – also known as lozenges or pastilles; they are
discoid shaped solid containing the medicinal agent in a
suitably flavored base.
• CACHETS – related to capsules in as such as they provide
an edible container for oral administration of solid
drugs.
• PELLETS – small, sterile cylinders about 3.2 mm in
diameter by 8 mm in length, formed by compression
from medicated masses
33. • AEROSOLS – both oral and topical; they contain
therapeutically active ingredients dissolved, suspended, or
emulsified in a propellant or in a mixture of solvent and
propellant
• RADIOPHARMECUTICALS – radioisotopes used in
medicine for therapeutic and diagnostic purposes
34. BIOLOGICAL PRODUCTS
Vaccines a suspension of attenuated (live) or inactivated
(killed) microorganisms or fraction thereof administered
to induce immunity and thus prevent infectious disease.
Toxoid – a modified antigen from an infectious organism
used as a vaccine
Immune globulin – a solution containing antibodies
from the pooled plasma of not less than 1,000 normal
individuals
Hyperimmune serum – a special preparation obtained
from human donor polls selected for high antibody titer
against a specific disease
37. Five reasons for the need for dosage
forms.
1. To protect the drug substance from destructive influences of
atmospheric oxygen
2. To protect the drug from the destructive influence of gastric acid after
oral administration
3. To conceal the bitter, salty, or offensive taste or odor of a drug
substance.
4. To provide liquid preparations of substance that are insoluble in desired
vehicle
5. To provide for insertion of a drug into one of the body’s orifices
6. To provide optimal drug action from topical administration sites, etc.
40. Advantages and disadvantages of
different dosage forms
• Ease of administrations
• Stability purposes
• Portability/ conveniently carried
• Elegance
• Accurate dosage
• Manufactured at lower cost
• Optimal drug action and others
41. PRESCRIPTION
from the Latin words: prae – before and scribo – I write. A
prescription is an order for medication issued by a physician,
dentists, veterinarian or other properly licensed
practitioner.
42. Prescription contains a specific drug and dosage to be
prepared or dispensed by a pharmacist and administered to a
particular patient.
A prescription is preprinted forms containing the name,
address, contact number, and other relevant information
regarding physician or other prescriber. Also a blank spaces
used by the prescriber in providing information about the
patient, the medication desired, and the directions for use.
43. Parts of Prescription
1. Prescriber’s Information. The name of the physician
or dentist, his specialty, clinic address, contact number
and clinic hours.
2. Patient information. The full name and address of
the patient are necessary for identification purposes.
3. Date. Prescriptions are dated at the time they are
written. The date is important in establishing the
medication record of the patient especially in filling
prescriptions for controlled substances
44. Parts of Prescription
4. Rx Symbol or Superscription. The Rx symbol is a Latin verb recipe,
meaning take thou or you take
5. Medication Prescribed or Inscription. Body or main part of the of the
Rx order. It contains the names and quantities of the prescribed ingredients or
drugs, dosage form and potency
The name of the product must be written both in
Nonproprietary (generic name)
Proprietary (brand)
Chemical
Dosage form- the physical entity of medication (tablet, capsule)
Strength – potency of drug (250 mg, 100IU)
Quantity to be dispensed – this includes the amount and the unit of
measure (grams, milligrams, tablets)
45. Parts of Prescription
6. Dispensing Directions to Pharmacist or Subscription.
Directions to the pharmacist for preparing the prescription
These can be used for:
Preparations (compounding)
Labeling ( information to be put on the label )
7. Directions for the Patient or Transcription. Instructions on
the number of dosage units per dose (one tablet), route of
administration, frequency of dosing (every 4 hours), duration of dosing
(one week, for one month) and use of the drug (optional)
46. Parts of Prescription
• 8. Refill Information. If refill information is not
supplied, it is generally assumed that no refills are
authorized
• 9. Prescriber’s Signature. The name and signature
of the physician or dentist who wrote the prescription
order. Below the signature of the physician are the
licensed number to practice his profession, PTR
( Privilege Tax Receipt) no. and TIN
47.
48. Parts of Prescription Order
1. Prescriber Information and Signature
2. Patient Information
3. Date Prescription was written
4. Superscription
5. Inscription
6. Subscription
7. Signa
8. Special Instructions (Optional)
50. Filling and Recording Procedures
1. The prescription once filled must be retained by the
pharmacist for a period of two years
2. The prescription must be recorded in Rx book and
ready for inspection by BFAD FDRO’s when the outlet
is open for operation anytime
51. Questions
1. Enumerate at least two responsibilities of the pharmacist
in providing the medication needs of the patient
a. Provide information about drugs to the health profession
and to the public legally responsible for dispensing
prescription.
b. Translate and communicate the dangers of drug to
the patient, and others
52. Questions
2. Enumerate the instructions that pharmacist should be given
to the patient in filling, refilling and dispensing legend
prescriptions
A. Filling of Prescriptions
danger of overdosage
side effects
proper storage for stability
need to discard unused medication
dangers to be mixed in one container
53. B. Refilling Prescription
a. taking drugs for longer period of time unless it is
under supervision
b. taking other medications with identical composition
which provides the same therapeutic effect which are
sometimes prescribed by other doctor
c. taking food found in the diets that are contraindicated
to the prescribed drugs
d. letting other members of the family or friends to
use his medicine
54. C. Dispensing Prescription
a. the proper use of drugs
b. the need to discontinue the use of the drug if certain
reactions develop
c. the need to see the doctor if serious reactions develop,
if the condition has been a long term problem
d. the danger of using the OTC drugs when
prescribed medication is the possible duplication of the
drug or therapeutic action
e. the danger of self-diagnosis and self medication
55. A. Based on the number of ingredients
1. Simple prescription – with only one ingredient
2. Compound prescription – with one more than one ingredient
3. Polypharmacal prescription – with ten or more than ten ingredients
B. Magistral prescription – is a prescription which is prescribed very
often by the same doctor, of the same ingredients, and compounded by
the same pharmacist
C. Coded prescription is also called “blind prescription” and consists of
words, symbols, to represent the name of the drugs. This is unethical practice of
doctors and pharmacist
3. Enumerate the types of Prescription based on the number of
ingredients
56. INTERPRETATIONS
1. Nembutal 100 mg (at bed time) ( if there is a need) ( by mouth )
2. Propranolol hydrochloride 40 mg (by mouth) (twice a day)
3. Ampicillin 1 g (Intavenous piggyback) (every 6 hours)
4. Demerol 50 mg (Intramuscularly) (every 4 hours) (if there is a need)
for pain
5. Tylenol 325 mg tablets (2) (by mouth) (at once, immediately)
6. Pilocarpine (2) (drops) (both eyes) (every 3 hours)
7. Scopolamine 0.8 mg (subcutaneously) (immediately)
8. Milk of magnesia 1 (tablespoon) (by mouth) (at bed time) (every night)
9. Septra DS tablet (double strength) (1) (every day) (by mouth)
62. Prescription written
by authorized
prescriber
Patient presents
prescription to the
pharmacy
Prescription is checked for
completeness; prescriber
info, drug name, strength,
dose, and directions
Correct patient info is
entered into computer
system
Prescription is prepared.
Correct amount of med
prescribed is measured and
placed into container
Pharmacy label is generated.
Make sure all the legal items
are identified
Prescription is interpreted and
confirmed by pharmacy system.
Third party is billed online (optional)
Prescription is prepared by
pharmacy technician, and
final check done by
pharmacist
Patient receives script, pharmacy
assistant must offer counseling to the
patient. Then script is rung on cash
register, and insurance log signed
Pharmacist provides counseling
on the medication prescribed and
all medically related questions
R
LABEL
63. 1. How is a prescription processed?
receiving the prescription
reading and checking the
prescription
numbering and dating
Labeling
preparing the prescription
packaging
rechecking
delivering and patient
counseling
recording and filling
pricing the prescription
64. 3. What is the purpose of numbering
and dating the prescription?
The same number of the original prescription should appear
at the label of the filled prescription – to avoid error in
dispensing
The date of the prescription is not the same date that should
be placed on the filled prescription – for identification
purposes
65. 4. Information to be recorded in the
prescription book.
1. name of physician
2. name of the drug
3. quantity
4. date when dispensed
5. balance (quantity if any)
6. pharmacist signature, etc
71. Where more than one drug product is prescribed on one
prescription form.
72. What to do with erroneous
prescriptions
Erroneous prescriptions shall be filed. Such prescription shall
also be kept and reported by the pharmacist of the drug
outlet or any other interested party to the nearest DOH
office for appropriate action.
75. Where the generic name is not legible and a brand name which is
legible is written
76. When the brand name is indicated and instructions added (such as the phrase " no
substitution") which tend to obstruct, hinder or prevent proper generic dispensing.
77. What to do with violative prescriptions
Violative prescriptions shall not be filed. They are
kept and reported by the pharmacist of drug
outlet or any other interested party to the nearest
DOH office for appropriate action. The pharmacist
shall advise the prescriber of the problem and/or
instruct the customer to get the
proper prescription.
81. When both the generic name and the brandname are not legible
82. When the drug product prescribed is not registered with FDA
83. What to do with impossible
prescriptions
Impossible prescription shall not be filed. They shall be and
reported by the pharmacist of drug outlet or any other
interested party to the nearest DOH office for appropriate
action. The pharmacist shall advise the prescriber of the
problem and/or instruct the customer to get the proper
prescription.