Pharmacology is the science of drugs, including their names, effects on the body, and clinical uses. It has two main divisions: pharmacokinetics, which studies what the body does to drugs, and pharmacodynamics, which studies what drugs do to the body. Drugs come from natural sources like plants, animals and microbes, or they can be synthesized chemically. A prescription provides instructions from a healthcare provider to a pharmacist regarding a specific medication for a particular patient, including the name, dose, directions, and other important information. Prescriptions must follow standard formats and include additional details for controlled substances due to their potential for abuse.
Ganglionic stimulants like nicotine can activate nicotinic receptors in autonomic ganglia, resulting in the stimulation of both sympathetic and parasympathetic responses. Although they have limited medical use, nicotine has been used experimentally to help identify nerve fibers. Ganglionic blockers are competitive antagonists at nicotinic receptors that reduce autonomic tone, and were once used to treat hypertension and peptic ulcers but caused intolerable side effects. Trimethaphan is a short-acting ganglionic blocker occasionally used for controlled hypotension. Mecamylamine has been studied for smoking cessation by blocking nicotine's rewarding effects but also causes constipation. Currently there is no significant
The document discusses local anesthetics, including their definition, classification, mechanisms of action, pharmacokinetics, clinical applications, and adverse effects. Specifically, it notes that local anesthetics reversibly block sodium channels to produce localized numbness, and are classified based on their chemical structure as esters or amides. Common examples like lidocaine, bupivacaine, and benzocaine are also mentioned.
Presentation for Medical undergraduates for teaching pharmacology. It deals with Physiology of steroid hormones and their action along with agents which are used therapeutically with their action, adverse effects and therapeutic uses.
Lecture slides for undergraduates medical (MBBS) Students. Source material for this presentation is Essentials of Pharmacology, KD Tripathi, Katzung and Goodman and Gillman. It deals with Local anaesthetics with their mechanism of action, pharmacokinetics , adverse effects and therapeutic uses.
1) Aminoglycosides are polybasic amino groups linked glycosidically to aminosugar compounds. They are highly water soluble and excreted unchanged in urine.
2) They are bactericidal, inhibiting protein synthesis by binding to the 30S/50S interface of bacterial ribosomes. This causes misreading of mRNA and nonfunctional protein formation.
3) Common adverse effects include ototoxicity (hearing loss) and nephrotoxicity. Individual drugs vary in their specific toxicities.
It is a anti- hypertensive drug. It is non-selective beta blocker drug. Hence it is beta blocker drug so it has many side effect.Not only Propranolol but also Timolol,Atenolol are beta blocker drugs.
Analgesics are drugs that relieve pain without causing unconsciousness. They are divided into opioid and non-opioid categories. Opioid analgesics include natural opium alkaloids like morphine and codeine, semi-synthetic opiates, and synthetic opioids. They act on opioid receptors in the brain. Non-opioid analgesics include NSAIDs like aspirin and ibuprofen, which reduce pain and inflammation by inhibiting prostaglandin synthesis. Acetaminophen is also a non-opioid analgesic. Both opioid and non-opioid analgesics can cause side effects like hypersensitivity, peptic ulcers, liver damage, and renal toxicity when taken in excess.
Ganglionic stimulants like nicotine can activate nicotinic receptors in autonomic ganglia, resulting in the stimulation of both sympathetic and parasympathetic responses. Although they have limited medical use, nicotine has been used experimentally to help identify nerve fibers. Ganglionic blockers are competitive antagonists at nicotinic receptors that reduce autonomic tone, and were once used to treat hypertension and peptic ulcers but caused intolerable side effects. Trimethaphan is a short-acting ganglionic blocker occasionally used for controlled hypotension. Mecamylamine has been studied for smoking cessation by blocking nicotine's rewarding effects but also causes constipation. Currently there is no significant
The document discusses local anesthetics, including their definition, classification, mechanisms of action, pharmacokinetics, clinical applications, and adverse effects. Specifically, it notes that local anesthetics reversibly block sodium channels to produce localized numbness, and are classified based on their chemical structure as esters or amides. Common examples like lidocaine, bupivacaine, and benzocaine are also mentioned.
Presentation for Medical undergraduates for teaching pharmacology. It deals with Physiology of steroid hormones and their action along with agents which are used therapeutically with their action, adverse effects and therapeutic uses.
Lecture slides for undergraduates medical (MBBS) Students. Source material for this presentation is Essentials of Pharmacology, KD Tripathi, Katzung and Goodman and Gillman. It deals with Local anaesthetics with their mechanism of action, pharmacokinetics , adverse effects and therapeutic uses.
1) Aminoglycosides are polybasic amino groups linked glycosidically to aminosugar compounds. They are highly water soluble and excreted unchanged in urine.
2) They are bactericidal, inhibiting protein synthesis by binding to the 30S/50S interface of bacterial ribosomes. This causes misreading of mRNA and nonfunctional protein formation.
3) Common adverse effects include ototoxicity (hearing loss) and nephrotoxicity. Individual drugs vary in their specific toxicities.
It is a anti- hypertensive drug. It is non-selective beta blocker drug. Hence it is beta blocker drug so it has many side effect.Not only Propranolol but also Timolol,Atenolol are beta blocker drugs.
Analgesics are drugs that relieve pain without causing unconsciousness. They are divided into opioid and non-opioid categories. Opioid analgesics include natural opium alkaloids like morphine and codeine, semi-synthetic opiates, and synthetic opioids. They act on opioid receptors in the brain. Non-opioid analgesics include NSAIDs like aspirin and ibuprofen, which reduce pain and inflammation by inhibiting prostaglandin synthesis. Acetaminophen is also a non-opioid analgesic. Both opioid and non-opioid analgesics can cause side effects like hypersensitivity, peptic ulcers, liver damage, and renal toxicity when taken in excess.
NSAIDs have analgesic, antipyretic and anti-inflammatory properties. They work by inhibiting cyclooxygenase (COX) enzymes and reducing prostaglandin production. NSAIDs are classified as nonselective COX inhibitors like aspirin, preferential COX-2 inhibitors like nimesulide, or selective COX-2 inhibitors like celecoxib. Common adverse effects include gastrointestinal irritation. NSAIDs are used to treat pain, fever, and inflammation conditions like arthritis.
This document discusses anticholinergic drugs, with a focus on atropine. It provides details on:
- Atropine's mechanism of action as a competitive muscarinic receptor blocker.
- Its pharmacological effects including mydriasis, tachycardia, dry mouth, constipation, and increased body temperature.
- Therapeutic uses such as a pre-anesthetic, to treat peptic ulcers, bronchospasm, Parkinson's disease, and motion sickness.
- Atropine poisoning symptoms and treatment involving gastric lavage and physostigmine administration.
- Atropine substitutes like hyoscine butylbromide and ipratrop
This document discusses quinolones and fluoroquinolones, including their history, mechanisms of action, classifications, spectra of activity, and examples like ciprofloxacin. It notes that nalidixic acid was the first quinolone introduced in the 1960s but had limited potency. Fluoroquinolones were developed in the 1980s by adding a fluorine group, improving potency and spectra against both gram-positive and gram-negative bacteria. Examples discussed include ciprofloxacin, norfloxacin, ofloxacin, moxifloxacin, and newer agents like prulifloxacin and delafloxacin. Adverse effects are generally mild
A Powerpoint presentation on drugs excretion and elimination suitable for UG medical students. This ppt is already presented to my students in one of the theory classes.
Pharmacokinetics is the study of how the body affects drugs. It involves absorption, distribution, metabolism and excretion of drugs. Absorption refers to how drugs enter systemic circulation from the site of administration. Distribution is the movement of drugs between tissues via blood flow. Metabolism involves chemical alteration of drugs by oxidation, reduction and conjugation reactions. Excretion is the removal of drugs and metabolites from the body. Together, these processes determine the effects of drugs over time.
Anti-adrenergic drugs antagonize the action of adrenaline and related drugs by competitively blocking alpha and/or beta receptors. Alpha blockers such as prazosin are used to treat hypertension and benign prostatic hyperplasia by dilating arteries and reducing prostate tone. Beta blockers like propranolol non-selectively block both beta 1 and 2 receptors and are used for hypertension, angina, arrhythmias and migraine. Drugs for glaucoma work by reducing intraocular pressure through various mechanisms such as decreasing aqueous humor production or increasing outflow.
This presentation discusses drug antagonism, which occurs when one drug inhibits the action of another drug. There are four types of antagonism: physical, chemical, physiological/functional, and pharmacological. Pharmacological antagonism can be competitive or non-competitive. Competitive antagonism occurs when two drugs bind to the same receptor site, such that increasing the concentration of one drug can overcome the effects of the other. Non-competitive antagonism occurs when an antagonist binds to a site other than the agonist site and prevents receptor activation by the agonist. Examples of competitive and non-competitive antagonism in receptor pharmacology are provided.
Pharmacology of Penicllins (Beta lactam antibiotics), description of their mechanism of action, mechanism of resistance, classification, indications and adverse effects
This presentation deals with the various non-steroidal antiinflammatory drugs used in day-to-day practice enumerating their mechanism of action, uses, adverse effects, etc.
This document discusses histamine and antihistamine drugs. It begins by introducing histamine as an amine mediator involved in inflammatory and hypersensitivity reactions. Histamine is synthesized from the amino acid histidine and stored in mast cells. It is released during allergic reactions and acts on receptors to cause effects like gastric acid secretion, vasodilation, smooth muscle contraction and itch sensation. Antihistamines work by competing with histamine for receptors to block its actions. They are used to treat allergic disorders, insect bites, pruritus and other conditions. Common side effects include sedation, dry mouth and blurred vision.
This document summarizes opioids and their use as analgesics. It discusses the classification of opioids as natural, semi-synthetic, or synthetic and describes their mechanisms of action through mu, delta, and kappa receptors in the central nervous system. The document outlines the pharmacokinetics of opioid absorption, distribution, metabolism, and excretion. It also discusses the clinical uses of opioids like morphine, as well as their side effects, risks of overdose and addiction, and treatment options for opioid overuse.
Clinical Pharmacokinetics-I [half life, order of kinetics, steady state]BADAR UDDIN UMAR
This document discusses key concepts in pharmacokinetics including half-life, steady state concentration, and clearance. It explains that half-life refers to the time it takes for a drug concentration to reduce by half and impacts dosing frequency. Steady state occurs when drug administration equals elimination within a dosing interval, resulting in constant levels. Clearance represents the ability of organs to remove drug from the bloodstream and is used to determine maintenance doses. The document provides examples of these principles and their clinical significance.
This ppt discusses pharmacological actions, toxic effects and clinical applications of corticosteroids. It also mentions precations to be taken while using steroids
Unit 1 General Pharmacology (As per PCI syllabus)Mirza Anwar Baig
This document provides an overview of general pharmacology. It defines key terms like pharmacology, drugs, routes of drug administration, essential drugs concept, and orphan drugs. It describes the major routes of drug administration including topical, oral, parenteral, rectal, and inhalation. For each route, it discusses advantages, disadvantages, and examples. The document aims to explain the essential characteristics of drugs for proper absorption and excretion and summarize the roles of distribution and metabolism in drug actions.
Expt 8 Effect of drugs on ciliary motility of frog oesophagusMirza Anwar Baig
This document outlines a study to examine the effect of various drugs on gastrointestinal motility using frogs. The study will use physostigmine and atropine solutions applied to the buccal cavity of frogs to measure the time taken for food particles to move from the lower jaw to the esophagus, compared to a saline control. The goal is to determine if physostigmine enhances while atropine reduces gastrointestinal motility by stimulating or blocking acetylcholine, respectively. The procedure describes preparing the frog, taking baseline measurements, then applying the drug solutions and remeasuring motility times to observe any effects.
This document discusses lipoproteins and drugs that lower lipid levels. It begins by defining lipoproteins and how they transport lipids in blood, classifying them into six groups. It then discusses the functions of different lipoproteins and causes of hyperlipoproteinemias. The document focuses on statins, how they work by inhibiting HMG-CoA reductase, and their effects on cholesterol, LDL, HDL, and triglyceride levels. It covers the pharmacokinetics of statins, their adverse effects and uses. Other drug classes discussed include bile acid sequestrants, fibrates, nicotinic acid and their mechanisms and uses for treating different lipid abnormalities.
This document provides information on analgesics and anti-inflammatory drugs. It begins by defining analgesics as drugs that relieve pain without altering consciousness, and anaesthesia as loss of sensation. It then classifies analgesics into two main groups - opioid analgesics like morphine and non-opioid analgesics like NSAIDs. The document goes on to describe various opioid and non-opioid analgesics in detail, their mechanisms of action, uses, and adverse effects. It focuses on the role of prostaglandins in pain and inflammation, and how different NSAIDs work by inhibiting prostaglandin synthesis.
This document discusses drugs used for local and general anesthesia. It describes how local anesthetics work by blocking sodium ion channels to prevent nerve impulses, and discusses different delivery techniques including infiltration, nerve blocks, and spinal/epidural anesthesia. It also covers the pharmacological properties and systemic effects of local anesthetics, noting they can cause vasodilation, cardiac depression at high doses, and lower blood pressure. The document compares features of local and general anesthesia and categorizes local anesthetics based on onset, potency, and duration of action.
This document discusses antacids, which are basic substances that neutralize gastric acid and raise the pH of gastric contents. It describes the normal physiology of gastric acid secretion and factors that can increase secretion. Increased acid can lead to discomfort, inflammation, ulcers, and cancer. Antacids are classified as systemic or non-systemic. Systemic antacids like sodium bicarbonate are absorbed but can cause alkalosis, while non-systemic antacids like magnesium hydroxide, aluminum hydroxide, and calcium carbonate react locally in the stomach. Combination antacids contain fast- and slow-acting components to provide prompt and sustained relief without systemic effects or disturbing bowel movements.
This document provides an overview of general anesthetics, including their definition, mechanisms of action, stages of anesthesia, classifications, and examples. It discusses inhalational anesthetics like nitrous oxide, halothane, sevoflurane and desflurane, outlining their properties such as potency, solubility, and side effects. It also reviews intravenous anesthetics including thiopental, propofol, ketamine and etomidate, noting their mechanisms, onsets, durations and side effect profiles. The document is intended to educate about the different types of general anesthetics used in surgery to induce reversible unconsciousness and muscle relaxation.
1.introduction to different dosage formsGaju Shete
This document introduces different dosage forms for drug delivery. It discusses traditional forms like tablets, capsules, and injections as well as novel forms like implants, controlled drug delivery systems, liposomes, nanoparticles, prodrugs, and films/strips. Implants can be opened or closed using magnets to control drug release and are placed under the skin. Controlled drug delivery systems embed drugs in polymeric matrices for slow release over long periods. Liposomes, erythrocytes, and nanoparticles can encapsulate drugs for targeted or prolonged delivery. Prodrugs are converted to active drugs after metabolism to improve properties. Films and strips provide topical delivery of drugs over time.
NSAIDs have analgesic, antipyretic and anti-inflammatory properties. They work by inhibiting cyclooxygenase (COX) enzymes and reducing prostaglandin production. NSAIDs are classified as nonselective COX inhibitors like aspirin, preferential COX-2 inhibitors like nimesulide, or selective COX-2 inhibitors like celecoxib. Common adverse effects include gastrointestinal irritation. NSAIDs are used to treat pain, fever, and inflammation conditions like arthritis.
This document discusses anticholinergic drugs, with a focus on atropine. It provides details on:
- Atropine's mechanism of action as a competitive muscarinic receptor blocker.
- Its pharmacological effects including mydriasis, tachycardia, dry mouth, constipation, and increased body temperature.
- Therapeutic uses such as a pre-anesthetic, to treat peptic ulcers, bronchospasm, Parkinson's disease, and motion sickness.
- Atropine poisoning symptoms and treatment involving gastric lavage and physostigmine administration.
- Atropine substitutes like hyoscine butylbromide and ipratrop
This document discusses quinolones and fluoroquinolones, including their history, mechanisms of action, classifications, spectra of activity, and examples like ciprofloxacin. It notes that nalidixic acid was the first quinolone introduced in the 1960s but had limited potency. Fluoroquinolones were developed in the 1980s by adding a fluorine group, improving potency and spectra against both gram-positive and gram-negative bacteria. Examples discussed include ciprofloxacin, norfloxacin, ofloxacin, moxifloxacin, and newer agents like prulifloxacin and delafloxacin. Adverse effects are generally mild
A Powerpoint presentation on drugs excretion and elimination suitable for UG medical students. This ppt is already presented to my students in one of the theory classes.
Pharmacokinetics is the study of how the body affects drugs. It involves absorption, distribution, metabolism and excretion of drugs. Absorption refers to how drugs enter systemic circulation from the site of administration. Distribution is the movement of drugs between tissues via blood flow. Metabolism involves chemical alteration of drugs by oxidation, reduction and conjugation reactions. Excretion is the removal of drugs and metabolites from the body. Together, these processes determine the effects of drugs over time.
Anti-adrenergic drugs antagonize the action of adrenaline and related drugs by competitively blocking alpha and/or beta receptors. Alpha blockers such as prazosin are used to treat hypertension and benign prostatic hyperplasia by dilating arteries and reducing prostate tone. Beta blockers like propranolol non-selectively block both beta 1 and 2 receptors and are used for hypertension, angina, arrhythmias and migraine. Drugs for glaucoma work by reducing intraocular pressure through various mechanisms such as decreasing aqueous humor production or increasing outflow.
This presentation discusses drug antagonism, which occurs when one drug inhibits the action of another drug. There are four types of antagonism: physical, chemical, physiological/functional, and pharmacological. Pharmacological antagonism can be competitive or non-competitive. Competitive antagonism occurs when two drugs bind to the same receptor site, such that increasing the concentration of one drug can overcome the effects of the other. Non-competitive antagonism occurs when an antagonist binds to a site other than the agonist site and prevents receptor activation by the agonist. Examples of competitive and non-competitive antagonism in receptor pharmacology are provided.
Pharmacology of Penicllins (Beta lactam antibiotics), description of their mechanism of action, mechanism of resistance, classification, indications and adverse effects
This presentation deals with the various non-steroidal antiinflammatory drugs used in day-to-day practice enumerating their mechanism of action, uses, adverse effects, etc.
This document discusses histamine and antihistamine drugs. It begins by introducing histamine as an amine mediator involved in inflammatory and hypersensitivity reactions. Histamine is synthesized from the amino acid histidine and stored in mast cells. It is released during allergic reactions and acts on receptors to cause effects like gastric acid secretion, vasodilation, smooth muscle contraction and itch sensation. Antihistamines work by competing with histamine for receptors to block its actions. They are used to treat allergic disorders, insect bites, pruritus and other conditions. Common side effects include sedation, dry mouth and blurred vision.
This document summarizes opioids and their use as analgesics. It discusses the classification of opioids as natural, semi-synthetic, or synthetic and describes their mechanisms of action through mu, delta, and kappa receptors in the central nervous system. The document outlines the pharmacokinetics of opioid absorption, distribution, metabolism, and excretion. It also discusses the clinical uses of opioids like morphine, as well as their side effects, risks of overdose and addiction, and treatment options for opioid overuse.
Clinical Pharmacokinetics-I [half life, order of kinetics, steady state]BADAR UDDIN UMAR
This document discusses key concepts in pharmacokinetics including half-life, steady state concentration, and clearance. It explains that half-life refers to the time it takes for a drug concentration to reduce by half and impacts dosing frequency. Steady state occurs when drug administration equals elimination within a dosing interval, resulting in constant levels. Clearance represents the ability of organs to remove drug from the bloodstream and is used to determine maintenance doses. The document provides examples of these principles and their clinical significance.
This ppt discusses pharmacological actions, toxic effects and clinical applications of corticosteroids. It also mentions precations to be taken while using steroids
Unit 1 General Pharmacology (As per PCI syllabus)Mirza Anwar Baig
This document provides an overview of general pharmacology. It defines key terms like pharmacology, drugs, routes of drug administration, essential drugs concept, and orphan drugs. It describes the major routes of drug administration including topical, oral, parenteral, rectal, and inhalation. For each route, it discusses advantages, disadvantages, and examples. The document aims to explain the essential characteristics of drugs for proper absorption and excretion and summarize the roles of distribution and metabolism in drug actions.
Expt 8 Effect of drugs on ciliary motility of frog oesophagusMirza Anwar Baig
This document outlines a study to examine the effect of various drugs on gastrointestinal motility using frogs. The study will use physostigmine and atropine solutions applied to the buccal cavity of frogs to measure the time taken for food particles to move from the lower jaw to the esophagus, compared to a saline control. The goal is to determine if physostigmine enhances while atropine reduces gastrointestinal motility by stimulating or blocking acetylcholine, respectively. The procedure describes preparing the frog, taking baseline measurements, then applying the drug solutions and remeasuring motility times to observe any effects.
This document discusses lipoproteins and drugs that lower lipid levels. It begins by defining lipoproteins and how they transport lipids in blood, classifying them into six groups. It then discusses the functions of different lipoproteins and causes of hyperlipoproteinemias. The document focuses on statins, how they work by inhibiting HMG-CoA reductase, and their effects on cholesterol, LDL, HDL, and triglyceride levels. It covers the pharmacokinetics of statins, their adverse effects and uses. Other drug classes discussed include bile acid sequestrants, fibrates, nicotinic acid and their mechanisms and uses for treating different lipid abnormalities.
This document provides information on analgesics and anti-inflammatory drugs. It begins by defining analgesics as drugs that relieve pain without altering consciousness, and anaesthesia as loss of sensation. It then classifies analgesics into two main groups - opioid analgesics like morphine and non-opioid analgesics like NSAIDs. The document goes on to describe various opioid and non-opioid analgesics in detail, their mechanisms of action, uses, and adverse effects. It focuses on the role of prostaglandins in pain and inflammation, and how different NSAIDs work by inhibiting prostaglandin synthesis.
This document discusses drugs used for local and general anesthesia. It describes how local anesthetics work by blocking sodium ion channels to prevent nerve impulses, and discusses different delivery techniques including infiltration, nerve blocks, and spinal/epidural anesthesia. It also covers the pharmacological properties and systemic effects of local anesthetics, noting they can cause vasodilation, cardiac depression at high doses, and lower blood pressure. The document compares features of local and general anesthesia and categorizes local anesthetics based on onset, potency, and duration of action.
This document discusses antacids, which are basic substances that neutralize gastric acid and raise the pH of gastric contents. It describes the normal physiology of gastric acid secretion and factors that can increase secretion. Increased acid can lead to discomfort, inflammation, ulcers, and cancer. Antacids are classified as systemic or non-systemic. Systemic antacids like sodium bicarbonate are absorbed but can cause alkalosis, while non-systemic antacids like magnesium hydroxide, aluminum hydroxide, and calcium carbonate react locally in the stomach. Combination antacids contain fast- and slow-acting components to provide prompt and sustained relief without systemic effects or disturbing bowel movements.
This document provides an overview of general anesthetics, including their definition, mechanisms of action, stages of anesthesia, classifications, and examples. It discusses inhalational anesthetics like nitrous oxide, halothane, sevoflurane and desflurane, outlining their properties such as potency, solubility, and side effects. It also reviews intravenous anesthetics including thiopental, propofol, ketamine and etomidate, noting their mechanisms, onsets, durations and side effect profiles. The document is intended to educate about the different types of general anesthetics used in surgery to induce reversible unconsciousness and muscle relaxation.
1.introduction to different dosage formsGaju Shete
This document introduces different dosage forms for drug delivery. It discusses traditional forms like tablets, capsules, and injections as well as novel forms like implants, controlled drug delivery systems, liposomes, nanoparticles, prodrugs, and films/strips. Implants can be opened or closed using magnets to control drug release and are placed under the skin. Controlled drug delivery systems embed drugs in polymeric matrices for slow release over long periods. Liposomes, erythrocytes, and nanoparticles can encapsulate drugs for targeted or prolonged delivery. Prodrugs are converted to active drugs after metabolism to improve properties. Films and strips provide topical delivery of drugs over time.
The document defines key terms related to pharmacology and drug administration. It discusses drug nomenclature, classification, sources, constituents, dosage forms, routes of administration, and factors affecting absorption and distribution. Pharmacokinetics are also summarized, including the processes of absorption, distribution, metabolism, and excretion that determine a drug's movement through the body.
This document provides an overview of pharmacology and mechanisms of drug action. It defines pharmacology as the study of drug interaction with living organisms. Key points include: drugs can come from natural, animal, mineral or laboratory sources; various routes of administration depend on factors like physical properties and site of action; pharmacodynamics examines how drugs affect the body by interacting with receptors, ion channels, enzymes or through chemical reactions; and pharmacogenetics considers genetic differences in metabolic pathways that influence drug responses.
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”.
Pharmacology is the study of drugs and their interaction with living systems. It has two main divisions: pharmacodynamics, which is what the drug does to the body, and pharmacokinetics, which is what the body does to the drug. Drugs can be administered through several routes depending on whether local or systemic action is needed. Common routes include oral, sublingual, rectal, cutaneous, inhalation, nasal, subcutaneous, intramuscular, intravenous, and intradermal injection. The choice of route depends on factors like drug properties and patient condition.
Unit-1: General pharmacology :Introduction to pharmacologySabaShaikh76
Introduction to Pharmacology- Definition and scope of pharmacology, nature and source of drugs, essential drugs concept and routes of drug administration, spare receptors, addiction, tolerance, dependence, tachyphylaxis, idiosyncrasy, allergy
This document defines key terms and concepts in pharmacology. It discusses how pharmacology is the study of drugs and their interactions with living systems. It defines pharmacokinetics as what the body does to the drug and pharmacodynamics as what the drug does to the body. It describes different drug sources, dosage forms, routes of administration, and the processes of absorption, distribution, metabolism, and excretion that determine a drug's behavior in the body. It also discusses receptor theory, drug interactions, and synergism.
This document discusses various routes of drug administration including oral, parenteral, sublingual, rectal, nasal, and others. It provides details on each route, including advantages and disadvantages. The parenteral route is described in further detail, outlining specific methods such as intravenous, intramuscular, intradermal, subcutaneous, and others.
The document provides information on general pharmacology concepts. It defines pharmacology as the study of drugs and their interaction with living systems. It describes the key processes involved in pharmacokinetics as absorption, distribution, metabolism and excretion (ADME). Absorption refers to how the drug enters the bloodstream. Distribution involves the transport of drug molecules within the body. Metabolism is how drugs are broken down and biotransformed by the body. Excretion is the removal of drugs from the body, mainly through the kidneys or bile.
The document provides information on general pharmacology concepts. It defines pharmacology as the study of drugs and their interaction with living systems. It describes the key processes involved in pharmacokinetics as absorption, distribution, metabolism and excretion (ADME). Absorption refers to how the drug enters the bloodstream. Distribution involves the transport of drug molecules within the body. Metabolism is how drugs are broken down and biotransformed by the body. Excretion is the removal of drugs from the body, mainly through the kidneys or bile.
This presentation deals with the basic pharmacology orientation course everyone (newbies which may include MBBS undergrads, nursing staff, b. pharma. students, etc.) must get themselves acquainted with
Introduction to pharmacology- Mr. Pannehabdou panneh
Pharmacology is the study of how drugs interact with living systems. It includes the study of drug action, interaction, effects, and properties. There are two main branches - pharmacodynamics which examines how drugs act on the body, and pharmacokinetics which examines how the body acts on drugs. Adverse drug reactions can occur and are influenced by several factors. It is important for nurses to understand pharmacology to properly administer medications and recognize potential adverse effects.
INTRODUCTION TO PHARMACOLOGY PHARMACOKINETICS AND DYNAMICSKaishAamirPathan
This document provides an introduction to the fields of pharmacology, pharmacodynamics, and pharmacokinetics. It defines pharmacology as the study of drugs and their interactions with living systems. The key divisions of pharmacology are pharmacodynamics, which refers to how drugs act on the body, and pharmacokinetics, which describes how the body affects drugs. Several routes of drug administration are described including oral, sublingual, rectal, inhalation and others. The sources and essential concepts regarding drugs are also outlined.
This document discusses general pharmacology concepts including definitions of key terms like pharmacokinetics and pharmacodynamics. It covers topics like the chemical nature and sources of drugs, drug names and classifications. It also examines concepts related to how drugs are absorbed, distributed, metabolized and excreted by the body. Specifically, it discusses factors that influence drug absorption like physicochemical properties and physiological factors. It also addresses drug distribution and the volume of distribution concept. The document provides an overview of fundamental pharmacology topics.
Pharmacology is the study of drugs and their interaction with living systems. It has several branches including pharmacodynamics, pharmacokinetics, pharmacotherapy, toxicodynamics, clinical pharmacology, and pharmacogenetics. Drugs come from natural sources like plants, animals and microorganisms, or they can be synthesized. They are prepared in various dosage forms for administration via different routes. Solid dosage forms include tablets, capsules, powders, while semi-solid forms include ointments, gels and creams. Liquid forms include solutions, suspensions, emulsions, syrups and elixirs. Proper drug administration and understanding their effects and movement in the body is important in clinical practice.
Pharmacology is the study of how drugs interact with living systems. It has two main areas - pharmacokinetics, which examines what the body does to drugs, and pharmacodynamics, which examines what drugs do to the body. There are several factors that influence drug absorption including the route of administration, physicochemical properties of the drug, dosage form, and concentration of the drug. Absorption involves movement of the drug from its site of entry into blood or lymph without chemical change, and can occur via passive diffusion, active transport, or endocytosis.
This document discusses various topics related to pharmacology including:
1. Pharmacology is defined as the study of the action of drugs on biological systems, incorporating aspects of medicine and biology.
2. Pharmacokinetics is the process by which drugs are absorbed, distributed, metabolized and excreted by the body over time.
3. Drugs can come from natural sources like plants, animals and microbes, or be synthesized chemically. Their effects can be studied through pharmacodynamics and pharmacotherapeutics.
Pharmacology is the study of how drugs interact with living systems. It involves understanding the physiological and biochemical effects of drugs, their mechanisms of action, absorption, distribution, metabolism, and excretion. Key terms include drug, chemotherapy, toxicology, and orphan drugs. Essential drugs are those that address priority healthcare needs and are selected based on safety, efficacy, and cost-effectiveness. Drugs can be administered through various local and systemic routes including oral, rectal, intravenous, intramuscular, subcutaneous, intradermal, transdermal, nasal, inhalational, and sublingual.
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Test bank for karp s cell and molecular biology 9th edition by gerald karp.pdfrightmanforbloodline
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How to Control Your Asthma Tips by gokuldas hospital.Gokuldas Hospital
Respiratory issues like asthma are the most sensitive issue that is affecting millions worldwide. It hampers the daily activities leaving the body tired and breathless.
The key to a good grip on asthma is proper knowledge and management strategies. Understanding the patient-specific symptoms and carving out an effective treatment likewise is the best way to keep asthma under control.
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A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Histololgy of Female Reproductive System.pptxAyeshaZaid1
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
The skin is the largest organ and its health plays a vital role among the other sense organs. The skin concerns like acne breakout, psoriasis, or anything similar along the lines, finding a qualified and experienced dermatologist becomes paramount.
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These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
7. Explain the role of peripheral chemoreceptors in regulation of respiration
8. Explain the regulation of respiration during exercise
9. Integrate the respiratory regulatory mechanisms
10. Describe the Cheyne-Stokes breathing
Study Resources:
1. Chapter 42, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 36, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 13, Human Physiology by Lauralee Sherwood, 9th edition
5-hydroxytryptamine or 5-HT or Serotonin is a neurotransmitter that serves a range of roles in the human body. It is sometimes referred to as the happy chemical since it promotes overall well-being and happiness.
It is mostly found in the brain, intestines, and blood platelets.
5-HT is utilised to transport messages between nerve cells, is known to be involved in smooth muscle contraction, and adds to overall well-being and pleasure, among other benefits. 5-HT regulates the body's sleep-wake cycles and internal clock by acting as a precursor to melatonin.
It is hypothesised to regulate hunger, emotions, motor, cognitive, and autonomic processes.
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
2. Definitions
Pharmacology
– Pharmakon : drug
– Logos: Science
• Is the science that deals with the drugs names,
pharmacokinetics, pharmacodynamics, side effects
and clinical uses.
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3. Main Divisions
• Pharmacology is mainly divided into two parts:
1. Pharmacokinetics
What the body does to the drug?
2. Pharmacodynamics
What the drug does to the body?
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5. Pharmacology:
Pharmacokinetics
• Are studies of the
– Absorption
– Distribution
– Metabolism
– Excretion
Pharmacodynamics
• Are studies of
- Mechanisms of drug action (MOA)
- Pharmacological effects (therapeutic effects & toxic effects)
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6. Other subdivisions of Pharmacology …
• Pharmacogenomics: The study of genetic influences on
the effectiveness and fate of drugs
• Toxicology: the study of the adverse or toxic effects of
drugs and other chemical agents
• Therapeutics: Medical treatment of disease
• Pharmacoeconomics: compares the value of one
pharmaceutical drug or drug therapy to another
• Pharmacoepidemiology: is the study of the use and the
effects of drugs in large numbers of people
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7. What is a drug?
• A drug is any chemical substance that modify
physiological system or pathological state and can
be used for diagnosis, prevention or treatment of
disease.
• When administered appropriately, drug can cause
a range of physiological and
biochemical/molecular changes in a complex
biological system that relate to its composition,
structure and target
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8. Where do drugs come from?
• Plants
• Human-derived proteins/steroids
• Fungi/bacteria
• Synthetic chemicals
• Recombinant proteins
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9. I. General Principles of Pharmacology
1. Sources and Nature of Drug Dosage Form
2. Prescription Writing
3. ------
4. -----
5. -----
6. -----
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10. Sources and Nature of Drug Dosage
Form
Modern drugs are obtained from many sources:
1. 50% of total prescriptions are composed of
synthetic or semisynthetic (based on natural
active ingredients) chemical agents
Natural:
1. 25% contain plant resources
2. 12% are microbial-derived products
3. 7% are mineral in character
4. 6% are animal-derived
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11. Classification of drug sources
• Natural sources of drugs
1. Plants: the whole plant, leaves, root, bark,
seeds, flowers
2. Microorganisms: bacteria, fungi, …
3. Minerals
4. Animals: organs, tissues, fluids
• Synthetic sources of drugs
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12. Natural sources of drugs, examples
Plants
• The active ingredients might be found in any part (or all
parts) of the plant
Microorganisms
• Microbial metabolites used as drugs, especially the
antibiotics and antineoplastic agents. Examples:
1. a strain of mold Penicillium chrysogenicum produces
Penicillin G
2. Clavulanic acid is a product of fungus Streptomyces
species
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13. Natural sources of drugs
3. Minerals
1. Purified sulfur is used internally only, as a
laxative
4. Animals
Animal sources: organs, tissues, fluids:
1. Beef and pork pancreas are the source of the
natural insulin sold today
2. Exogenous thyroxine can be obtained from the
thyroid glands of animals, usually pigs
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14. Synthetic sources of drugs
• Many new drugs have been synthesized.
• Semisynthetic drugs are based on natural
ingredients:
1. Morphine and synthetic analgesics
2. Hormones, vitamins, synthetic antibiotics are
only a small part of the modern drugs,
produced by synthesis.
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16. DRUG DOSAGE FORMS
CLASSIFICATION OF DRUG DOSAGE FORMS
Drug substances are developed into drug dosage forms in
order to optimize stability, safety and effectiveness of drug
substances and to make them suitable for administration.
According to the consistence, they are classified as:
1. Solid dosage forms
2. Liquid dosage forms
3. Semisolid dosage forms
4. Aerosols
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17. Characteristics of solid dosage forms
• POWDERS
• oral powders – e.g., antacid and laxative
powders
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18. TABLETS
Tablets prepared by compression. This is the
most frequently used dosage form of
administering a drug.
Tablet types and their abbreviations:
compressed (or plain) tablets (CT) – These
tablets are formed by compression and
contain no special coating. E.g. paracetamol
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19. Sublingual tablets
• small and dissolve rapidly.
• they are placed under the tongue and allowed to
dissolve after absorption
• the drug enters the systemic circulation without
passing through the portal circulation, thus avoiding
first-pass inactivation in the liver
• Drugs that are destroyed by the GI fluids or are
subject to 1st pass metabolism may be formulated
into such tablets. E.g: Nitroglycerin
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20. • chewable tablets are large, hard tablets,
difficult to swallow, intended to be crushed
before ingesting.
• effervescent tablets contain sodium
bicarbonate and an organic acid in addition to
the drug substance. In the presence of water,
these additives react liberating carbon dioxide
which acts as disintegrator and produces
effervescence. E.g. Vit C
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21. • film-coated tablets (FCT):
are compressed tablets which are covered with
a thin layer or a film of polymeric substances to
protect their contents from moisture or to mask
the taste of the ingredients. e.g:
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22. enteric-coated tablets (ECT)
• are coated with substances that resist solution in
gastric fluid but disintegrate in the alkaline contents
of the intestine.
• Enteric coating is used for drugs with a gastric
irritant action, for drugs which are unstable in the
acid medium of the gastric contents or if the drug
should act on the intestine. e.g., Diclofenac Na.
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24. CAPSULES
Capsules are solid dosage forms in which the drug
substance is enclosed in either a hard or soft soluble
container of suitable form of gelatin:
• Hard gelatin capsules
• Soft elastic capsules (SEC) are soft, gelatin shells
somewhat thicker than that of hard gelatin.
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25. GRANULES
• Granules are dosage forms related to
powders. They are particularly suitable for the
preparation of solutions or mixtures of drugs,
such as antibiotics, that are unstable in the
presence of water
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26. CHARACTERISTICS OF LIQUID DOSAGE
FORMS
• SOLUTIONS
Solutions are homogeneous mixtures that are
prepared by dissolving a solid, liquid, or gas in
another liquid.
• EMULSIONS
Emulsions are two-phase systems that are
normally immiscible in which one liquid is
dispersed throughout another liquid in the form of
small droplets.
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27. SUSPENSIONS
Suspensions are two-phase systems consisting
of finely divided solids dispersed in liquids. If the
drug is insoluble or poorly soluble, a suspension
may be the most suitable dosage form.
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28. DROPS
Drops are intended to be administered
internally or externally (as eye drops or
collyrium, nasal, and otic drops). Drops are
prescribed in small quantity (10 – 30 g).
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29. STERILE DOSAGE FORMS FOR
INJECTION
• They differ from all other drug dosage forms because
of their unique use for injection directly into body
tissue through the primary protective systems of the
human body, the skin and mucous membranes.
Therefore, they must be exceptionally pure and free
from contaminants
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30. CHARACTERISTICS OF SEMISOLID
DOSAGE FORMS
OINTMENTS are semisolid preparations
intended for external application to the skin or
mucous membranes.
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31. TYPES OF OINTMENTS
• OINTMENTS (oil 80% - water 20%) are prepared of
solid active ingredients (1–25%), finely powdered and
then incorporated into the oleaginous base. They can
be: ointments for skin application, eye ointments, nose
ointments.
• PASTES contain powders dispersed in the vehicle in
quantity more than 25%. They are usually stiffer, less
greasy and more absorptive than ointments. Pastes
adhere reasonably well to the skin and they are suited
for application on and around moist lesions.
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32. • CREAMS: similar to ointments. A cream is an
emulsion of oil and water in approximately
equal proportions
• GELS or jellies are semisolid dosage forms
with high degree of clarity, ease of application
and ease of removal and use. The active
ingredients are incorporated into water-
soluble bases. The gels often provide a faster
release of drug substance as compared to
creams and ointments.
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33. • SUPPOSITORIES
Suppositories are solid dosage forms of various
weights and shapes for insertion into the rectum or
vagina
• PLASTERS
Plasters are substances intended for external
application. They are intended to bring medication into
close contact with the skin. medicated plasters are
used for local or regional drug delivery
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34. AEROSOLS (SPRAY)
• These drugs are designed to carry the drug into the respiratory tree of the
patient or on the skin and mucous (nasa, etc.)
• Aerosols are heterogeneous systems consisting of very finely subdivided
liquid or solid particles (optimum size 0,5–3 μm) dispersed in a gas
medium. They can be inhaled (nasally or orally) or applied topically to
dispense a variety of agents for treatment of systemic and topical
diseases.
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35. Nebulizers
• Nebulizers are devices used for administration of solutions giving
sufficiently small droplets.
• Advantages: rapid onset of action; bypass the hepatic circulation;
avoidance of degradation in the GI tract; lower dosage that minimizes
adverse reactions; simple, convenient and acceptable therapy.
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37. History
• Prescriptions have been in use since ancient times
– Latin adopted as standard language
– “Rx” = prescription
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38. Definition
A prescription is a
written, verbal, or
electronic order
from a practitioner
or designated agent
to a pharmacist for a
particular
medication for a
specific patient.
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40. Current Prescription Formatting
• Heading
–Name, address, and telephone
number of the prescriber
–Name, sex and age of the patient
–Date of the prescription
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42. Current Prescription Formatting
• Body
–The Rx symbol
–Name
–dose size or concentration
(liquids) of the drug
–Amount to be dispensed
–Directions to the patient
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43. Contents of the “body”
• Name of the drug
AVOID THE USE OF:
–Abbreviations
• Many drugs identified with abbreviations
–EX: HCT for hydrochlorothiazide, MSO4
for morphine sulfate
• Attempts to standardize abbreviations
have been unsuccessful
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44. • Tablets - tab
• Capsule – cap
• Syrup – syr
• Suspension – susp
• Injection – Inj
• Metered dose inhaler – as such
• Lotion – as such
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49. Controlled Substances
Legally, drugs are classified into 3 categories:
1. OTC : Over The Counter drugs
2. POM : Prescription Only Medications
3. Controlled Drugs: - a prescription drug
whose use and distribution is tightly
controlled because of its abuse potential or
risk
• Regulation is more strict
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50. Prescription for controlled drugs must
(e.g. morphine)
1. Be completely written in the prescriber’s hand writing
in ink
2. Be signed & dated
3. Carry the prescribers’ address
4. Carry the name & address of the patient
5. State the form of the drug
6. State the total quantity of the drug or the number of
dose units to be disposed in both words & figures
7. State the exact size of each dose in both words &
figure. 50
51. CASE
A hypertensive patient accidentally received Vantin 200 mg
instead of Vasotec 20 mg when a pharmacist misread this
prescription
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52. MAXIMIZE PATIENT SAFETY
• ALWAYS space out words and numbers to
avoid confusion.
• ALWAYS complete medication orders.
• AVOID abbreviations.
• When in doubt, ask to verify.
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53. Summary:
Contents of the Prescription
–Date of the order
–Patient Name and Address
–Name of the drug
–Strength of the drug
–Quantity of the drug
–Directions for use
–Practitioner Name, Address, Telephone
number
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54. Grouping of drugs:
Pharmacologic class (or family):
– drugs that share similar characteristics
– Example: beta-adrenergic blockers are an example
of a pharmacologic class.
Therapeutic class:
– groups drugs by therapeutic use.
– Example: Antihypertensives
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