This document provides an overview of key concepts in pharmacology for nursing students. It discusses the following main points in 3 sentences or less:
Pharmacology is the study of drugs and their effects on the body. It utilizes concepts from biology, pathology, and chemistry to understand drug therapies. The history of pharmacology dates back to ancient times when various cultures applied natural remedies, and it began to emerge as a modern science in the 19th century with the isolation of active drug components.
The FDA and other regulatory agencies were created to standardize drugs and ensure they are safe and effective through various laws and standards. The FDA specifically regulates drug approval and safety through three centers that oversee prescription drugs, biologics,
Pharmacology: Class Session 1 and 2 Introduction to PharmacologyMariaJose2001
This is an outline of the basics of Pharmacology. A discussion of how drugs are named, classified and its effects on the person's biochemical processes. It also included the factors influencing drug action and potential drug interactions. At the end, some commonly ysed terminologies were defined.
This is an introduction to Pharmacology, which is very helpful for nursing students. This presentation tells about classification, sources, pharmacokinetics, and pharmacodynamics of drugs.
Pharmacology: Class Session 1 and 2 Introduction to PharmacologyMariaJose2001
This is an outline of the basics of Pharmacology. A discussion of how drugs are named, classified and its effects on the person's biochemical processes. It also included the factors influencing drug action and potential drug interactions. At the end, some commonly ysed terminologies were defined.
This is an introduction to Pharmacology, which is very helpful for nursing students. This presentation tells about classification, sources, pharmacokinetics, and pharmacodynamics of drugs.
In a broad sense, the pharmacology deals with the study of drugs and their interactions with living systems. This study includes sources, chemical properties, dose, biological effects, therapeutic uses, and adverse effects of drugs. i.e. Pharmacology is the study of how drugs act on biological systems and how the body responds to the drug.
It comprises all aspects of knowledge about drugs, but most importantly those that are relevant to effective and safe use for medicinal purposes. Pharmacology integrates the knowledge of many disciplines, including medicine, pharmacy, dentistry, nursing, and veterinary medicine. This integrative nature allows pharmacology to make unique and significant contributions to human health.
Pharmacology is crucial for:
discovering new medicines to help fight diseases
improving the effectiveness of medicines
reducing unwanted side effects of medicines
understanding why individuals differ in the way they respond to certain drugs, and why some others cause addiction
. Introduction to Pharmacology Course Title: Pharmacology I Course No.: PHAR 2113 Prepared by: Biswajit Biswas Reference: Goodman & Gilman’s Manual of Pharmacology and Therapeutics
2. Pharmacology Greek pharmakon : "drug“ ; and logia : "the study of“. Greek: Pharmacon (Drug) Modern Latin: Pharmacologia 18th Century: Pharmacology The branch of medicine concerned with the uses, effects, and modes of action of drugs.
3. Historic development of pharmacology Worlds oldest pharmacology - from India and China Materia medica (2735 B.C.) by Pan Tsao- contained mainly Plant and metal with few animal products Ayurveda - described by Charaka accordig to Rigveda (3000 B.C.) - includes 300 vegetable drugs , classified into 50 groups according to their effects on symptoms. Papyrus (1500 B.C.) discovered by Eber -700 drugs Modern medicine (from 450 B.C.) by Hippocrates- concept of disease as a pathologic process and organize pharmacology on the basis of observation, analysis and deduction.- use simple and efficacious drugs.
4. Allopathay (James gregory, 1753-1821) -treatment without any rational basis- use symptomatic treatment with obnoxious remedis. Homeopathy (Hanneman, 19th century)-
Pharmacology is study of the substances which interact with living system by activating or inhibiting normal body processes. It includes physical and chemical properties, biochemical and physiological effects, mechanism of action, therapeutic uses and adverse effects of drugs.
Pharmacology is the branch of pharmaceutical sciences which is concerned with the study of drug or medication action, where a drug can be broadly defined as any man-made, natural, or endogenous molecule which exerts a biochemical or physiological effect on the cell, tissue, organ, or organism
In a broad sense, the pharmacology deals with the study of drugs and their interactions with living systems. This study includes sources, chemical properties, dose, biological effects, therapeutic uses, and adverse effects of drugs. i.e. Pharmacology is the study of how drugs act on biological systems and how the body responds to the drug.
It comprises all aspects of knowledge about drugs, but most importantly those that are relevant to effective and safe use for medicinal purposes. Pharmacology integrates the knowledge of many disciplines, including medicine, pharmacy, dentistry, nursing, and veterinary medicine. This integrative nature allows pharmacology to make unique and significant contributions to human health.
Pharmacology is crucial for:
discovering new medicines to help fight diseases
improving the effectiveness of medicines
reducing unwanted side effects of medicines
understanding why individuals differ in the way they respond to certain drugs, and why some others cause addiction
. Introduction to Pharmacology Course Title: Pharmacology I Course No.: PHAR 2113 Prepared by: Biswajit Biswas Reference: Goodman & Gilman’s Manual of Pharmacology and Therapeutics
2. Pharmacology Greek pharmakon : "drug“ ; and logia : "the study of“. Greek: Pharmacon (Drug) Modern Latin: Pharmacologia 18th Century: Pharmacology The branch of medicine concerned with the uses, effects, and modes of action of drugs.
3. Historic development of pharmacology Worlds oldest pharmacology - from India and China Materia medica (2735 B.C.) by Pan Tsao- contained mainly Plant and metal with few animal products Ayurveda - described by Charaka accordig to Rigveda (3000 B.C.) - includes 300 vegetable drugs , classified into 50 groups according to their effects on symptoms. Papyrus (1500 B.C.) discovered by Eber -700 drugs Modern medicine (from 450 B.C.) by Hippocrates- concept of disease as a pathologic process and organize pharmacology on the basis of observation, analysis and deduction.- use simple and efficacious drugs.
4. Allopathay (James gregory, 1753-1821) -treatment without any rational basis- use symptomatic treatment with obnoxious remedis. Homeopathy (Hanneman, 19th century)-
Pharmacology is study of the substances which interact with living system by activating or inhibiting normal body processes. It includes physical and chemical properties, biochemical and physiological effects, mechanism of action, therapeutic uses and adverse effects of drugs.
Pharmacology is the branch of pharmaceutical sciences which is concerned with the study of drug or medication action, where a drug can be broadly defined as any man-made, natural, or endogenous molecule which exerts a biochemical or physiological effect on the cell, tissue, organ, or organism
Endocrine System Lesson PowerPoint, Hormones, Drugs, Additiction, Puberty, an...www.sciencepowerpoint.com
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This ppt is made for basic knowledge of pharmacology to any person.
Any non medical person can read this presentation and increase his/her knowledge for medicines and drugs.
in this presentation we explain medicine and it's importance in detail.
people can read about the medicine its classification and type of dose of injection.
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To study new drug registration process in u.sManoj Dagwar
Legislative History of Drug Regulation
Derived from the Dutch word meaning to boast (quacken), “quack” is the word Americans have commonly used to describe charlatans in medicine. Quacks peddled adulterated and mislabeled Medicines throughout the United States without penalty until 1906, when Congress passed the Food and Drugs Act, one section of which outlawed the practice.
Over the next half-century, Congress passed two major pieces of legislation expanding FDA Authority. It passed the Federal Food, Drug, and Cosmetic Act (FFDCA) in 1938, requiring that
Drugs be proven safe before they could be sold in interstate commerce. Then, in 1962, in the wake of deaths and birth defects from the tranquilizer thalidomide marketed in Europe, Congress passed the Kefauver-Harris Drug Amendments to the FFDCA,3 increasing safety provisions and
Requiring that drugs be proven effective as well.
Congress has amended the FFDCA many times, leading to FDA’s current mission of assuring
Americans that the medicines they use do no harm and actually work—that they are, in other words, safe and effective. In recent decades Congress has passed additional laws to boost
Pharmaceutical research and development and to speed the approval of new medicines.
FDA also regulates products other than drugs—for example, biological products, medical devices,
Dietary supplements, foods, cosmetics, animal drugs, and tobacco products. Sometimes the
Agency addresses issues that straddle two or more product types that the law treats differently.
How FDA Approves New Drugs
To market a prescription drug in the United States, a manufacturer needs FDA approval. to get that approval, the manufacturer must demonstrate the drug’s safety and effectiveness according to criteria specified in law and agency regulations, ensure that its manufacturing plant passes FDA inspection and obtain FDA approval for the drug’s labeling—a term that includes all written material about the drug, including, for example, packaging, prescribing information for physicians, and patient brochures.
The approval process begins before the law requires FDA involvement. Figure 1 illustrates a product’s timeline both before and during FDA involvement.
The research and development process for a finished drug usually begins in the laboratory. Basic research is often conducted or funded by the federal government.7 when basic research yields an idea that someone identifies as a possible drug component, government or private research groups focus attention on a prototype design. At some point, private industry (either a large, established company or a newer, smaller, start-up company) continues to develop the idea, eventually testing the drug in animals. When the drug is ready for testing in humans, the FDA must get involved.
The Standard Process of Drug Approval
The four FDA steps leading to the agency’s approval of a new drug for marketing in the United
States are described below.
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it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
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1. Pharmacology for Nurses Nur30 Mount Saint Mary’s College Associate Degree in Nursing Program Maggie Davis-Kendrick, RN,MSN
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Editor's Notes
Pharmacology
Exact starting date thought to begun in the early 1800s. If applied properly drugs can dramatically improve the quality of life
Covers traditional and, biological drug categories
Cover alternative drug therapy
In the early 1900, the U.S. developed and enforced tougher drug legislation to protect the public.
Refer to the book for other regulatory acts, legislation, standards and organizations., ,
The concerned addressed are is the drug effective, worsens other medical condition, does it interact safely with other medication, or affect one type of a pt. more than others.
The Prescription Drug User Fee Act and the FDA Modernization Act . have accelerated the approval process and required drug and biologic manufacturers to provide yearly product user fees
Drugs may be organized by their therapeutic or pharmacologic classification. . Two ways to classify drugs are by therapeutic classification and pharmacological classification. The fields of pharmacology and therapeutics are closely connected. Both areas are at the core of the nursing profession.
Drugs may be described by More practically classified by a portion of their chemical structure known as the chemical group name.
Some say generic are less effective
The term propriety suggest ownership
Conjugated used to describe a double chemical bond separated by a single bond.
Dependence- is a related term, often defined as a physiological or psychological need for a substance. When the drug is no longer available, the individual expresses physical signs of discomfort known as withdrawals
OTC drugs may have serious adverse effects (teaching ROY), they may react with food, other drugs and impair their ability to function safely and the potential for harm may increase if the disease is allowed to progress.
The “five rights” and “three checks” are guidelines to safe medication administration, they offer guidelines to be used during preparation, delivery and administration. Documentation of the time of administration and any associated side effects should be placed in the medical record.
For pharmacologic compliance, the patient must understand and personally accept the value associated with the prescribed drug regimen. Understanding the reasons for noncompliance can help the nurse increase the success of pharmacotherapy
Used in conjunction with the five rights and include checking. The fourth check is at the bedside when you tell the patient what you are giving them whether they can respond or not
The nurse must know the many abbreviations used to indicate dosing information. Agency policy often dictates the actual times that medications are given.
Per JACHO
ASAP- Usually within1 hours, STAT- usually twenty-thirty minutes or less. Single doses usually within 2hrs.
There are established orders and time schedules by which medications are routinely administered The nurse must understand factors which decrease compliance such as expense, annoying side effects and self-dosing with the medication.
Hs (noc) or hour of sleep
Prn orders do not follow this time schedule instead start from the time the medication is given
The nurse must have a comprehensive knowledge of the actions and side effects of drugs before they are administered. This understanding takes into account the actions and side effects of the drug as well as the physical and emotional needs of each patient.
Three broad categories , each has advantages and disadvantages
Sublingual route not suitable for extended release
NGT is soft and flexible advanced through the nostril into the stomach. GT is surgically into the stomach for patients who need long term care. Both require a functioning G.I. Tract. Other forms of oral (enteral) drug administration include syrups, elixirs, emulsions and suspensions( drugs consisting of 2 chemical agents that separate rapidly, therefore be sure to shake to mix thoroughly
Medication may taste nasty, liquid medicine may cause nausea, pills maybe hard to swallow
Mucous membranes are the eyes, ears, nose, respiratory tract, urinary tract, vagina, and rectum
Landmarks: 2 finger widths down from the acromion process; the bottom edge is at an imaginary line drawn from the axilla.
Landmarks: Draw an imaginary line between the greater trochanter and the posterior superior iliac spine; at the middle of the imaginary line, go up about one inch Safe but poses greatest danger for irritation of the sciatic nerve Avoid areas that look inflamed, edematous, or irritated and areas that contain moles, birthmarks, scars or other lesions.
Landmarks: With thumb toward the umbilicus, place palm of hand on the greater trocanter, index finger on the anterior superior iliac spine, and the middle finger on the iliac crest.
Landmarks: Place one hand below the greater trocanter and one hand above the lateral femoral condyle; mid-lateral thigh.
Hold firm pressure with one hand, watch the veins pop out
One of the most dangerous once the drug is given it cannot be retrieved. Has potentional for prolonged, contentious administration. Avoids tissue irritation or injury resulting from SQ or IM administration.
Parenteral administration results in a rapid onset of drug action. Because of the possibility of introducing microbes directly into the body, Parenteral routes are considered invasive and require aseptic technique. IV administration offers the fastest onset of action and is the most dangerous
Pharmacokinetics is the way that the body deals with a drug - how drug moves throughout the body. Pharmacodynamics explains how drugs produce changes in the body.
Physiological relating to the way that living things function, rather than to their shape or structure
Diffusion – flow, circulation, transmission. (example NA+ normal level 135-140) pt level 157 (high, give D5W (if not diabetic) at 100cc/hr (lower concentration) the sodium moves from it’s higher site toward the dextrose and water the lower concentration. Gradient –slope, incline, grade. Electrochemical -studies chemical change associated with electrons and electricity
pH partitioning Drugs will accumulate on which-ever side of a membrane that favors their ionization . So keeping in mind that an acid will ionize in an alkaline environment, and a base will ionize in an acidic environment we can determine in which environment a drug will accumulate. The processes involved in pharmacokinetics must be considered when choosing the most effective dose, route and schedule for a drug's use.
Lipid solubility is an important characteristic, because it determine how quickly a drug is absorbed, mixes within the bloodstream, crosses membranes and becomes localized in body tissues Ionization process by which an atom or molecule loses or gains electrons ,acquiring and electric charge or changing an existing charge. The blood-brain and fetal-placental barriers represent areas in the body where drug distribution may be limited. Lipid-soluble and non- ionized drugs easily cross these barriers; water-soluble and ionized drugs do not.
Physiological factors that may affect blood flow include
Avoided by Parenteral administration of drugs that undergo rapid hepatic metabolism many drugs absorbed across the intestinal tract are routed directly to the liver, which deactivates them before they can be distributed to body tissues. Usually require higher doses
Primary site of excretion are the kidneys. Water- soluble drugs may be secreted into saliva, sweat, and breast milk. As a drug moves through the body, it must cross membranes
Several important pharmacokinetics principles can be illustrated by measuring serum drug levels
Plasma half –life is an essential pharmacokinetic variable. Drugs with short half-lives must be given more frequently than those with long half-lives.
which is the “average” or standard dose of a medication. ED 50 represents the dose required to produce a therapeutic response in 50% of a specific population of patients. The lethal dose is determine in per- clinical trials as part of the drug development process. The therapeutic index offers the nurse practical information on the safety of a drug
The higher the potency, the less dose is needed to produce a response. The higher the efficacy, the greater the response
Responses to medications are caused by drug-receptor interactions
At receptors, drugs mimic or block the action of the body's own regulatory molecules
It is hoped that responses that have labeled idiosyncratic can someday be avoided through DNA testing. The very nature of pharmacology requires that the practitioner consider the specifics of age, growth, development, and weight in relation to pharmacokinetics and pharmacodynamics It is hoped that responses that have labeled idiosyncratic can someday be avoided through DNA testing. The very nature of pharmacology requires that the practitioner consider the specifics of age, growth, development, and weight in relation to pharmacokinetics and pharmacodynamics
In order to contribute to safe and effective pharmacotherapy, it is essential for the nurse to comprehend and apply fundamental concepts of growth and development. Nurses must possess an understanding of what is considered normal, in terms of growth and developmental patterns, so that deviations from the norm can be identified and health pattern impairments can be appropriately addressed.
Infants require special treatment due to their small size and their immature physiologic and biochemical processes.
Because liver and kidney are immature drugs will greater impact due to prolong duration of action
Giving medication to this age group can be challenging. Avoid placing medication in milk, O.J., or cereal. Oral medication that taste bad should be placed in jam, syrup, or fruit puree if possible.
In general, principles of medication administration that oretain to toddlers apply to this age group.
Health status of younger adults is generally good; absorption, metabolic, and excretion mechanism are at their peak
Because adults are living longer
The American Nurses Association publishes a list of ethical principles that nurses can use to guide their decision making. Nurse practice acts are enacted by every state to define the scope of practice of professional nursing and to protect the public
The State nursing practice acts, define what a nurse can and cannot do. Check the physician’s orders against the MAR to be certain the correct drugs have been administered.
Causes may include omission of one of the “five rights” or giving medications based on verbal, illegible or incomplete orders
Use of the nursing process can help reduce the number of medication errors. Nurses should work and collaborate with others on the healthcare team to develop agency policies for the storage and handling of medicines.
Subjective what the patient says or perceives, objective- gathered through physical assessment, lab tests, and other diagnostic sources
After analyzing the assessment data, the nurse formulates patient-specific nursing diagnoses appropriate for the medications used. Diagnoses will form the basis for the other steps in the Nursing Process
Knowledge deficit and non-compliance are the diagnosis used most often. The goal of pharmacotherapy is safe administration with the best therapeutic outcome possible
Systems of measurement used in pharmacology include the metric, apothecary, and household systems
Rarely used
D5W Must know normal dosage for the medication given in %
To convert grains to grams divide grains by 15 or 16, to convert grams to grain multiply grams by 15 or 16, to convert minims to milliliters divide minims by 15 or 16