This document provides information on various classes of drugs used to treat different types of infections and diseases. It discusses narcotics and their uses, side effects, and nursing considerations. It also summarizes several classes of antibiotics like aminoglycosides, carbapenems, cephalosporins, quinolones, penicillins, sulfonamides, tetracyclines, and macrolides. Additionally, it covers drugs used to treat tuberculosis, leprosy, HIV/AIDS, and antifungal drugs.
I am Dr. Anil. this is my Lecture delivered to 3rd year MBBS for the subject of Pharmacology. These slides cover basics of Antifungal drugs mainly its pharmacology.
I am Dr. Anil. this is my Lecture delivered to 3rd year MBBS for the subject of Pharmacology. These slides cover basics of Antifungal drugs mainly its pharmacology.
Antiprotozoal drugs are a class of medication used to treat infections caused by protozoa, which are single-cell organisms that belong to the type of parasites. Protozoal infections occur throughout the world and are a major cause of morbidity and mortality in some regions such as Africa and South-East Asia.
Description on types of fungal organisms with differences between bacteria and fungi. A note on useful and harmful fungi. Brief insight on Antifungal classification, mechanism of actions and pharmacological profile with drug of choices for various fungal infections.
The presentation gives an in-depth review of the Anti-fungal drugs used to treat various acute and chronic fungal infections along with their uses and MOA.
Antiprotozoal drugs are a class of medication used to treat infections caused by protozoa, which are single-cell organisms that belong to the type of parasites. Protozoal infections occur throughout the world and are a major cause of morbidity and mortality in some regions such as Africa and South-East Asia.
Description on types of fungal organisms with differences between bacteria and fungi. A note on useful and harmful fungi. Brief insight on Antifungal classification, mechanism of actions and pharmacological profile with drug of choices for various fungal infections.
The presentation gives an in-depth review of the Anti-fungal drugs used to treat various acute and chronic fungal infections along with their uses and MOA.
this slides includes overview of antimicrobial drugs, their classifications, antimicrobial resistance, adverse effects and toxicity, choice of antimicrobial drugs and its uses
Drugs active against atypical mycobacteria
Introduction
About 10% of mycobacterial infections seen in clinical practice in USA are not cozed by M tuberculosis or M tuberculosis complex organisms
But they are cozed nontuberculous or so-called "atypical" mycobacteria.
Atypical mycobacteria have distinctive lab x-tics
They are present in the environment & are not communicable frm person to person.
As a rule, these mycobacterial species are less susceptible than M tuberculosis to antituberculous drugs.
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
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Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS : UNIT 5
APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMS By - AKANKSHA ASHTANKAR
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
DISSERTATION on NEW DRUG DISCOVERY AND DEVELOPMENT STAGES OF DRUG DISCOVERYNEHA GUPTA
The process of drug discovery and development is a complex and multi-step endeavor aimed at bringing new pharmaceutical drugs to market. It begins with identifying and validating a biological target, such as a protein, gene, or RNA, that is associated with a disease. This step involves understanding the target's role in the disease and confirming that modulating it can have therapeutic effects. The next stage, hit identification, employs high-throughput screening (HTS) and other methods to find compounds that interact with the target. Computational techniques may also be used to identify potential hits from large compound libraries.
Following hit identification, the hits are optimized to improve their efficacy, selectivity, and pharmacokinetic properties, resulting in lead compounds. These leads undergo further refinement to enhance their potency, reduce toxicity, and improve drug-like characteristics, creating drug candidates suitable for preclinical testing. In the preclinical development phase, drug candidates are tested in vitro (in cell cultures) and in vivo (in animal models) to evaluate their safety, efficacy, pharmacokinetics, and pharmacodynamics. Toxicology studies are conducted to assess potential risks.
Before clinical trials can begin, an Investigational New Drug (IND) application must be submitted to regulatory authorities. This application includes data from preclinical studies and plans for clinical trials. Clinical development involves human trials in three phases: Phase I tests the drug's safety and dosage in a small group of healthy volunteers, Phase II assesses the drug's efficacy and side effects in a larger group of patients with the target disease, and Phase III confirms the drug's efficacy and monitors adverse reactions in a large population, often compared to existing treatments.
After successful clinical trials, a New Drug Application (NDA) is submitted to regulatory authorities for approval, including all data from preclinical and clinical studies, as well as proposed labeling and manufacturing information. Regulatory authorities then review the NDA to ensure the drug is safe, effective, and of high quality, potentially requiring additional studies. Finally, after a drug is approved and marketed, it undergoes post-marketing surveillance, which includes continuous monitoring for long-term safety and effectiveness, pharmacovigilance, and reporting of any adverse effects.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
51. Penicillins Effective, Safe Excreted Kidnes Risk of hypersensitivity Gram + bacteria Contraindications—hypersensitivity or allergic reactions; potential for cross-sensitivity with cephalosporins and carbapenems
52. Examples of Penicillins Dicloxacillin (Dynapen) Penicillin G Penicillin V (Pen-Vee K) Piperacillin (Pipracil)
61. Prototype Sulfa Preps Sulfamethoxazole Azo Gantanol Bactrim azo gantanol combo phenazopyridine and sulfa as a Antibiotic for UTI Bactrim combo trimethoprim and sulfa Antibiotic for UTI, PCP, ear infections, gonorrhea, etc. Sulfasoxazole Azogantrisin Pediazole azogantrisin combo phenazopyridine and sulfa for UTI’s Pediazole sulfisoxazole and erythromycin for otitis media
66. Macrolides and Ketolides May be bacteriostatic or bacteriocidal Erythromycin Telithromycin (Ketek)
67. Macrolides first intro in early 1950’s [erythromycin] inhibit growth of bacteria = bacteriostatic four main macrolides: erythromycin (many names) Azithromycin (Zithromax) Clarithromycin (Biaxin) troleandomycin
68. MACROLIDE: Indications for Use Widely used for respiratory tract and skin/soft tissue infections Used as penicillin substitute Used in newborns (ophthalmic)
69. Therapeutic EffectsMacrolides Strep infections Streptococcus pyogenes(group A beta-hemolytic) mild to moderate URTI Hemophilus influenza spirochetal infections syphilis & Lyme disease gonorrhea, chlamydia, and mycoplasma
70. Miscellaneous Metronidazole—effective against anaerobic bacteria, some gram+, and protozoa Quinupristin/dalfopristin— belongs to class streptogramins; bacteriostatic and bacteriocidal Spectinomycin—treatment of gonococcal exposure Vancomycin—active against gram+ Chloramphenicol—broad spectrum, bacteriostatic, active against gram+ and gram– Clindamycin—bacteriostatic, effective against gram+, some anaerobes Linezolid—member of new class oxalidinone; effective against aerobic gram+
71. Principles of Therapy Culture and sensitivity studies reviewed to treat with “right drug for right bug” Erythromycin interferes with the elimination of several drugs Monitor clients closely
72. Zithromax Loading dose of 500 mg Daily dose of 250 mg for total of 5 days therapy Given up t 10 days for CAP (community acquired pneumonia)
77. Tuberculosis (TB) Infectious disease that usually affects the lungs May infect lymph nodes, pleurae, bones, joints, kidneys, and GI tract Caused by Mycobacterium tuberculosis Multiplies slowly and remains dormant for years Natural history of TB Transmission Primary infection Latent tuberculosis infection (LTBI) Active tuberculosis
78. TB Principle organ affected is lungs Caused by Mycobacterium tuberculosis Transmission Primary infection Latent (LTBI)-Active TB
80. Chapter 34Drugs for Tuberculosis and Mycobacterium avium Complex (MAC) Disease
81. What does a positive PPD mean? Positive reaction is Induration NOT redness Low risk >15 mm >10 mm high risk >5mm persons at highest risk, HIV
82. Primary Antitubercular Drugs Rifapentine (Priftin)—used with at least one other drug; less frequent administration (1-2X/wk) Ethambutol (Myambutol)—part of 4-drug regimen Pyrazinamide—used with INH and rifampin for 2 mos Streptomycin—used in 4-drug regimen Isoniazid (INH)—most commonly used; bacteriocidal, inexpensive, and nontoxic Rifampin—works synergistically with INH Rifabutin (Mycobutin)—used in patients with HIV with MAC; longer half-life than rifampin
83. Secondary Antitubercular Drugs Para-aminosalicylic acid (PAS) Capreomycin (Capastat) Cycloserine (Seromycin) Ethionamide (Trecator SC) Indicated for clients when other agents are contraindicated or drug resistant
84. Other Drugs Used in Multidrug-Resistant Tuberculosis Aminoglycosides (amikacin and kanamycin) May be component of 4- to 6-drug regimen Fluoroquinolones (ciprofloxacin, levofloxacin, ofloxacin, and sparfloxacin) may be used
85. Resistant TB For INH-resistant TB—rifampin, pyrazinamide, and ethambutol for 6 mos
86. Resistant TB For rifampin-resistant TB—INH and ethambutol for 18 mos or INH, pyrazinamide, and streptomycin for 9 mos
87. Resistant TB MDR-TB—5- to 6-drug regimen individualized according to susceptibility reports
88. Resistant TB For intermittent schedules, healthcare providers administer or directly observe therapy (DOT)
89. Resistant TB During pregnancy—3-drug regimen of INH, rifampin, and ethambutol used with close monitoring of LFT
90. Mycobacterium Avium Complex Disease (MAC) Mycobatcteriumavium and Mycobacterium intracellulare are grouped together as MAC Found in water and soil; transmitted by inhalation of droplets Opportunistic infection of immunocompromised Main drugs used—macrolides, azithromycin and clarithromycin, and rifabutin Prophylactic therapy life-long 3-drug regimen—macrolide, rifabutin, and ethambutol
91. TB drugs first line agents ethambutol isoniazid pyrazinamide rifampin streptomycin second line agents paraaminosalicylate sodium (PAS) capreomycin cycloserine ethionamide kanamycin
92. Drugs used to Treat TB INH-Isoniazid Most common least expensive 300 mg/day or 900 mg 2x/week Adverse effects: Hepatotoxicity Peripheral neuropathy (Give B6-pyridoxine 25 to 50 mg daily)
93. Rifampin and Rifabutin Metabolized in liver SE: RED BODY FLUIDS GI irritation, hepatitis, Numerous drug interactions
94. Ethambutol Major adverse effect is optic neuritis Moniter visual acuity and red/green discrimination OK to give with food
95. Miscellaneous Drugs Chloramphenicol-Chloromycetin Used in serious infections Toxicity-life threatening blood dyscrasias Therapeutic levels 10-20mcg/mL “Gray baby syndrome” (cardiovascular collapse in newborns) Frequent CBC monitoring
96. Clindamycin (Cleocin) Rx Severe Infection Topical use - acne Diarrhea serious SE Persistent, bloody stools (>5 stools a day)—stop drug, assess for presence of C. Diff.
97. Vancomycin Gram + Used in serious infections Primarily IV PO for Rx of C.difficile Rx of MRSA Emergence of VRE IV – give slowly over 1-2 hrs to avoid RED MAN Syndrome
98. Viruses Viruses spread by secretions, ingestion, breaks in skin and mucous membranes, blood transfusions, sexual contact, pregnancy, breast-feeding, and organ transplantation Viral replication is parasitic in nature Viruses induce antibodies and immunity
99. Antiviral Drugs Few drugs inhibit viruses without being excessively toxic to host tissues Most antivirals inhibit viral replication but do not eliminate viruses from tissues Available drugs are expensive, relatively toxic, and effective in a limited number of infections
100. Drugs for Herpesvirus Infections Acyclovir, famciclovir, and valacyclovir Penetrate virus-infected cells, become activated by an enzyme, and inhibit viral DNA reproduction Treatment of herpes simplex and herpes zoster infections Cidofovir, foscarnet, ganciclovir, and valganciclovir Inhibit viral reproduction Treat cytomegalovirus (CMV) retinitis most commonly seen in AIDS Foscarnet treats acyclovir-resistant herpes simplex
101. Drugs for Influenza A Amantadine and rimantadine inhibit replication of the influenza A virus Oseltamivir (Tamiflu) and zanamivir (Relenza) approved for influenza A or B Seasonal prophylaxis used in high-risk patients Treat early and may shorten illness length
102. Drug for Respiratory Syncytial Virus (RSV) Ribavirin used to treat bronchiolitis or pneumonia caused by RSV Used in hospitalized infants and young children Given by inhalation with Viratek small particle aerosol generator
104. Drugs for HIV and AIDS (Antiretrovirals) See Handout in Class
105. Antifungal Drugs Mechanism of action is to disrupt the structure and function of various fungal cell components Polyenes and azoles act on ergosterol to disrupt fungal cell membranes Echinocandins or glucan synthesis inhibitors are a new class of antifungals that disrupt cell walls rather than cell membranes
106. Azoles Ketoconazole (Nizoral) given orally and is less toxic; little absorption occurs topically Disadvantage is there are many drug–drug interactions Fluconazole (Diflucan) Synthetic broad-spectrum agent that may be used long-term Increases effect of several drugs Itraconazole (Sporanox) Synthetic broad-spectrum agent similar to fluconazole May be used in long-term suppression of histoplasmosis Voriconazole (Vfend) Broad-spectrum activity
107. Polyenes Amphotericin B Highly toxic to humans and recommended only for serious, potentially fatal infections Nystatin Used topically only; too toxic for systemic use