Historic List of Awarded Graduate Degrees (PDF)

Total Page:16

File Type:pdf, Size:1020Kb

Historic List of Awarded Graduate Degrees (PDF) AUBURN UNIVERSITY COLLEGE OF VETERINARY MEDICINE BIOMEDICAL SCIENCES THESIS / DISSERTATION LISTING FROM 1932 - PRESENT GRADUATE DEGREES AWARDED COLLEGE OF VETERINARY MEDICINE BIOMEDICAL SCIENCES YEAR DEPARTMENT AUTHOR MAJOR PROFESSOR TITLE MS/PHD GRADUATED 1932 Unknown Moore, Mildred Unknown The Bacteriostatic Effect of Certain Dyes on the Species of the Genus Brucella. MS The Bacteriostatic Effect of Certain Dyes on Escherichia Coli, Salmonella Pullorum, MS 1932 Unknown Moore, Miriam Unknown and Eberthella Typhi. 1933 Unknown Wallace, Wyeth Stephens Unknown Bacteriology of Several Water Supplies Found in Lee County, Alabama. MS Duncan, Josephine MS 1936 Unknown Unknown The Growth of Mycobacterium Paratuberculosis. Dunning 1939 Pathology Greene, James Etheridge Unknown An Immunological Study of Canine Hematoza. MS Moore, Martha Eugenia MS 1939 Pathology Unknown The Helminth Parasites of Cottontail Rabbits in the Vicinity of Auburn, Alabama. Rutland 1940 Anatomy Mundhenk, Russell Lowell Unknown A Study of the Normal Adult Canine Hemogram. MS The Length of Time that Larvae of Equine Strongylus Survive in Pastures Under MS 1941 Pathology Woolf, Frank Perry Unknown Natural Conditions. 1942 Bacteriology MacNamee, James Kelly Unknown The Presence of Thermocuric Bacteria in Pasteurized Milk. MS Anatomy and The Histology and Hemopoietic Activity of the Spleen; A Comparative Study in MS 1944 Davis, Maud McCall Unknown Histology Domestic Animals. Pathology and Observations on the Life History of Cooperia Punctata (v. Linstow, 1907) Ransom, MS 1946 Bailey, Wilford Sherrill Unknown Parasitology 1907, a Nematode Parasite of Cattle. Large Animal MS Walter J. Gibbons and A Study of the Bacterial Flora of Alabama Dairy Cattle before and After Treatment with 1951 Surgery and Attleberger, Marie Hall Armin A. Leibold Aureomycin. Medicine 1951 Pathology Newberne, Paul Medford Charles S. Roberts The Anatomy and Physiology of the Normal and the Fur-Chewing Chinchilla . MS 2 GRADUATE DEGREES AWARDED COLLEGE OF VETERINARY MEDICINE BIOMEDICAL SCIENCES YEAR GRADUATED DEPARTMENT AUTHOR MAJOR PROFESSOR TITLE MS/PHD Larsen, Aubrey Dale A. Porter and MS 1951 Pathology Evaluation of Tuberculin Fractions and Johnin on Sensitized Guinea Pigs and Goats. Bartholomew Armin A. Leibold Pathology and MS 1952 Shelton, George Calvin Wilford S. Bailey A Study of Giardiasis in the Chinchilla. Parasitology Vardaman, Thomas Armin A. Leibold and The Effect of Various Chemical Agents on the Viability of Mycobacterium MS 1952 Pathology Hubert Dale A. Porter Paratuberculosi in Vitro. Studies on the Pathology of Leucocytozoon Simondi and Leucotycozoon Smithi MS 1954 Pathology Newberne, James Wilson Herman R. Seibold Infections. Charles S. Roberts and MS 1957 Pathology Turner, Leon Walker Experimental Leptospirosis in the Chinchilla (Chichilla laniger) . Ribelin Small Animal MS 1958 Surgery and Hobson, Howard Philip Benjamin F. Hoerlein Angiocardiography of the Canine Infected with Dirofilaria immitis. Medicine Anatomy, MS 1958 Physiology and Morgan, Horace C. Jr. Carl H. Clark A Comparison of Selected Liver Function Tests for Use in Veterinary Medicine . Pharmacology Physiology and A Comparison of Serum and Bone Alkaline Phosphatase Activity of Normal Dogs to MS 1959 Shields, Robert Pierce Carl H. Clark Pharmacology that of Dogs with Hypertrophic Pulmonary Osteoarthropathy. Small Animal MS 1959 Surgery and Wilcox, Howard Stuckey Benjamin F. Hoerlein Removal of Dirofilaria immitis by Pulmonary Arteriotomy in the Dog. Medicine Physiology and The Effects of Transfusion Methods and Donor Age on the Life Span of Red Blood MS 1959 Woodley, Charles H. Carl H. Clark Pharmacology Cells in Young Dogs. 3 GRADUATE DEGREES AWARDED COLLEGE OF VETERINARY MEDICINE BIOMEDICAL SCIENCES YEAR DEPARTMENT AUTHOR MAJOR PROFESSOR TITLE MS/PHD GRADUATED Small Animal MS A Preliminary Investigation to Determine the Practical Application of Keratoplasty for 1959 Surgery and Hayes, Frank Alfred Jr. Benjamin F. Hoerlein Canine Patients. Medicine Anatomy and An Experimental and Clinical Study of Toggle Pin Fixation of Recurrent Coxogemoral MS 1960 Durr, John L. James E. Greene Histology Luxation in the Dog. A Comparison of the Results of a Macroscopic Plate Test and Macroscopic Latex MS Crawford, Richard Paul 1961 Bacteriology James E. Neal Tube Test with the Results of the Agglutination Lysis Test for the Serological Jr. Diagnosis of Bovine Leptospirosis. Small Animal MS 1961 Surgery and Horne, Robert Dean Benjamin F. Hoerlein Clinical Evaluation of Pulmonary Arteriotomy for the Removal of Dirofilaria Immitis. Medicine Physiology and MS 1961 Kling, James Malcolm Moore J. Burns A Study of the Treatment of Pancreatic Insufficency in the Canine. Pharmacology Pathology and MS 1961 Lindsey, James Russell Wilford S. Bailey Some of the Factors Concerning Diagnosis of Canine Filariid Infections. Parasitology Physiology and The Effect of the Type of Dietary Protein and Carbohydrate on Cholesterol MS 1962 Farnell, Daniel R. Moore J. Burns Pharmacology Metabolism. Anatomy and MS 1962 Holloway, Clarke Lee Theodore C. Fitzgerald Macroscopic and Microscopic Anatomy of the Primary Olfactory Pathway of the Dog. Histology Physiology and Robertson, Benjamin MS 1962 Moore J. Burns A Study of Zinc Metabolism and the Zinc-Deficiency Syndrome in the Dog. Pharmacology Thomas Physiology and The Effects of Acute Infectious Canine Hepatitis on the Serum Components of the MS 1963 Beckett, Sidney Dwayne Moore J. Burns Pharmacology Canine. 4 GRADUATE DEGREES AWARDED COLLEGE OF VETERINARY MEDICINE BIOMEDICAL SCIENCES YEAR DEPARTMENT AUTHOR MAJOR PROFESSOR TITLE MS/PHD GRADUATED Anatomy and MS 1963 James, Charles Wesley Theodore C. Fitzgerald The Radiographic Anatomy of the Cerebral Arterial System of the Dog. Histology Pathology and MS 1963 Teer, Patricia Anne Wilford S. Bailey Toxic Hepatitis of the Dog Produced by Molds and Moldy Feed. Parasitology The Occurrence and Geographic Distribution of Q Fever Antibodies in Milk from MS 1963 Bacteriology Miller, William Robert James E. Neal Alabama Dairy Cattle. Large Animal MS 1963 Surgery and Vaughn, John Thomas Fred G. Schell Evaluation of Diodrast-I 131 to Test Renal Function in the Equine. Medicine Large Animal MS 1963 Surgery and Williams, David John III Walter J. Gibbons Examination of Bovine Cervical Mucus for the Diagnosis of Early Pregnancy. Medicine Small Animal MS Replacement of the Distal Thoracic Esophagus by Thoracic Relocation of the 1963 Surgery and Hoffer, Richard E. Benjamin F. Hoerlein Stomach. Medicine Pathology and Edwin J. Hoff and The Histopathology of Esophageal Granuylomas and Sarcomas Associated with MS 1964 Eubank, N. H. Parasitology Wilford S. Bailey Spirocerca Lupi Infection in the Dog. The Histopathology of Observations on the Nature of Lymphoid Nodules in Porcine MS 1964 Pathology Feldman, Roger Guy Charles S. Roberts Livers. Small Animal MS A Study of the Clinical Signs and Necropsy Findings Resulting from Experimentally 1964 Surgery and Few, Albert Braxton Benjamin F. Hoerlein Produced Lesions in the Canine Brain. Medicine Pathology and Gonzalez, Oswaldo Edwin J. Hoff & Wilford MS 1964 Pathogenesis of Canine Spirocercosis. Parasitology Lozano S. Bailey 5 GRADUATE DEGREES AWARDED COLLEGE OF VETERINARY MEDICINE BIOMEDICAL SCIENCES YEAR DEPARTMENT AUTHOR MAJOR PROFESSOR TITLE MS/PHD GRADUATED Physiology and A Comparison of Blood Urea and Urea Clearance Kidney Function Tests in the Equine MS 1964 Humburg, Jay M. Carl H. Clark Pharmacology Species. Physiology and The Effects of Chlorpromazine on the Blood Protein Level During Shock in Adult MS 1964 Soeharsono, Sulaeman Carl H. Clark Pharmacology Dogs. Physiology and MS 1964 Snow, Loran Martin Moore J. Burns The Effects of Infectious Canine Distemper on Certain Blood Components of the Dog. Pharmacology Physiology and MS 1966 Holloway, L. Shannon Jr. Carl H. Clark A Study of the Hemoglobin Variants in the Goat. Pharmacology Physiology and The Effect of the Type and Amount of Dietary Fat on Cholesterol Metabolism in the MS 1966 Mayo, Joseph G. Moore J. Burns Pharmacology Rat Monteith, Susan MS 1966 Unknown Reynolds M. Cody The Immunological Response in the Dog Associated with Spirocera Lupi Infection. Campbell Small Animal MS 1966 Surgery and Oliver, John E Jr. Benjamin F. Hoerlein Canine Cranial Surgery. Medicine Large Animal MS 1966 Surgery and Tijion, Joe Beng Walter J. Gibbons Studies on the Bovine Female Genital Organs. Medicine The Effects of Chymopapain on the Normal and Clinically Protruded Intervertebral MS 1966 Unknown Widdowson, Walter L. Unknown Disc and its Related Structures in the Dog (B. F. Hoerlein, Chm). Small Animal MS 1967 Surgery and Albert, Roosevelt A. Jr. Benjamin F. Hoerlein Canine Ventriculography and Encephalography. Medicine 6 GRADUATE DEGREES AWARDED COLLEGE OF VETERINARY MEDICINE BIOMEDICAL SCIENCES YEAR DEPARTMENT AUTHOR MAJOR PROFESSOR TITLE MS/PHD GRADUATED Physiology and MS 1967 Froe, Dreyfus L. II Carl H. Clark A Study of Hemoglobin Variants in Domestic Animals. Pharmacology 1967 Unknown Stott, George Goulding R. D. Whiteford Anatomy and Histology of the Female Genitalia of Coturnix Quail. MS Physiology and MS 1968 Cargill, Colin Frank Robert P. Shields Plasma Arginase as a Liver Function Test. Pharmacology Small Animal MS 1968 Surgery and Dorn, Albert Steven Benjamin F. Hoerlein Cerebral Angiography in the Dog; Methods, Interpretation and Clinical Application. Medicine Small Animal MS Canine Electroencephalography Using Acepromazine and Sodium Thiopental for 1968 Surgery
Recommended publications
  • Pharmaceutical Starting Materials/Essential Drugs
    BULLETIN MNS October 2009 PHARMACEUTICAL STARTING MATERIALS MARKET NEWS SERVICE (MNS) BI -MONTHLY EDITION Market News Service Pharmaceutical Starting Materials/Essential Drugs October 2009, Issue 5 The Market News Service (MNS) is made available free of charge to all Trade Support Institutions and enterprises in Sub-Saharan African countries under a joint programme of the International Trade Centre and CBI, the Dutch Centre for the Promotion of Imports from Developing Countries (www.cbi.nl). Should you be interested in becoming an information provider and contributing to MNS' efforts to improve market transparency and facilitate trade, please contact us at [email protected]. This issue continues the series, started at the beginning of the year, focusing on the leading markets in various world regions. This issue covers the trends and recent developments in eastern European pharmaceutical markets. To subscribe to the report or to access MNS reports directly online, please contact [email protected] or visit our website at: http://www.intracen.org/mns. Copyright © MNS/ITC 2007. All rights reserved 1 Market News Service Pharmaceutical Starting Materials Introduction WHAT IS THE MNS FOR PHARMACEUTICAL STARTING MATERIALS/ESSENTIAL DRUGS? In 1986, the World Health Assembly laid before the Organization the responsibility to provide price information on pharmaceutical starting materials. WHA 39.27 endorsed WHO‟s revised drug strategy, which states “... strengthen market intelligence; support drug procurement by developing countries...” The responsibility was reaffirmed at the 49th WHA in 1996. Resolution WHA 49.14 requests the Director General, under paragraph 2(6) “to strengthen market intelligence, review in collaboration with interested parties‟ information on prices and sources of information on prices of essential drugs and starting material of good quality, which meet requirements of internationally recognized pharmacopoeias or equivalent regulatory standards, and provide this information to member states”.
    [Show full text]
  • Pharmacology on Your Palms CLASSIFICATION of the DRUGS
    Pharmacology on your palms CLASSIFICATION OF THE DRUGS DRUGS FROM DRUGS AFFECTING THE ORGANS CHEMOTHERAPEUTIC DIFFERENT DRUGS AFFECTING THE NERVOUS SYSTEM AND TISSUES DRUGS PHARMACOLOGICAL GROUPS Drugs affecting peripheral Antitumor drugs Drugs affecting the cardiovascular Antimicrobial, antiviral, Drugs affecting the nervous system Antiallergic drugs system antiparasitic drugs central nervous system Drugs affecting the sensory Antidotes nerve endings Cardiac glycosides Antibiotics CNS DEPRESSANTS (AFFECTING THE Antihypertensive drugs Sulfonamides Analgesics (opioid, AFFERENT INNERVATION) Antianginal drugs Antituberculous drugs analgesics-antipyretics, Antiarrhythmic drugs Antihelminthic drugs NSAIDs) Local anaesthetics Antihyperlipidemic drugs Antifungal drugs Sedative and hypnotic Coating drugs Spasmolytics Antiviral drugs drugs Adsorbents Drugs affecting the excretory system Antimalarial drugs Tranquilizers Astringents Diuretics Antisyphilitic drugs Neuroleptics Expectorants Drugs affecting the hemopoietic system Antiseptics Anticonvulsants Irritant drugs Drugs affecting blood coagulation Disinfectants Antiparkinsonian drugs Drugs affecting peripheral Drugs affecting erythro- and leukopoiesis General anaesthetics neurotransmitter processes Drugs affecting the digestive system CNS STIMULANTS (AFFECTING THE Anorectic drugs Psychomotor stimulants EFFERENT PART OF THE Bitter stuffs. Drugs for replacement therapy Analeptics NERVOUS SYSTEM) Antiacid drugs Antidepressants Direct-acting-cholinomimetics Antiulcer drugs Nootropics (Cognitive
    [Show full text]
  • Execution by . . . Heroin?: Why States Should Challenge the FDA's Ban
    N2_BERGS_UPDATED (DO NOT DELETE) 1/15/2017 9:55 AM Execution by . Heroin?: Why States Should Challenge the FDA’s Ban on the Importation of Sodium Thiopental Matthew C. Bergs* ABSTRACT: This Note traces the history of the lethal injection drug shortage and its impact on how states carry out the death penalty. Though this topic has received much attention in recent years, relatively little attention has been paid to the D.C. Circuit’s decision in Cook v. FDA, which exacerbated the shortage. In Cook, the D.C. Circuit enjoined the FDA from exercising its enforcement discretion to allow the importation of sodium thiopental, the primary anesthetic used by states in lethal injection executions. This decision is significant because it effectively required the FDA to ban the importation of sodium thiopental, forcing states to find other ways to carry out executions. Many states have turned to new drugs and manufacturers, while others have returned to past methods of execution. However, states’ use of alternative drugs and manufacturers has had disastrous consequences, and the return to old methods of execution constitutes an unacceptable regression towards inhumane and barbaric punishment. Thus, this Note argues that states should make every effort to obtain sodium thiopental. Potential avenues to obtain the drug include adhering to the FDA’s regulations or litigating against the FDA’s regulations. Renewed access to sodium thiopental will resolve many of the problems plaguing the administration of lethal injection. I. INTRODUCTION & BACKGROUND .................................................. 762 A. HISTORY OF LETHAL INJECTION AS A METHOD OF EXECUTION ... 763 B. DEVELOPMENT OF THE LETHAL INJECTION DRUG SHORTAGE ....
    [Show full text]
  • 242 Part 522—Implantation Or Injectable Dosage Form
    Pt. 522 21 CFR Ch. I (4–1–11 Edition) PART 522—IMPLANTATION OR 522.723 Diprenorphine hydrochloride injec- tion. INJECTABLE DOSAGE FORM NEW 522.770 Doramectin. ANIMAL DRUGS 522.775 Doxapram. 522.778 Doxycycline hyclate. Sec. 522.784 Doxylamine succinate injection. 522.23 Acepromazine. 522.800 Droperidol and fentanyl citrate in- 522.44 Sterile sodium acetazolamide. jection. 522.46 Alfaprostol. 522.810 Embutramide, chloroquine, and lido- 522.56 Amikacin. caine solution. 522.62 Aminopentamide hydrogen sulfate in- 522.812 Enrofloxacin. jection. 522.820 Erythromycin. 522.82 Aminopropazine fumarate sterile so- 522.840 Estradiol. lution injection. 522.842 Estradiol benzoate and testosterone 522.84 Beta-aminopropionitrile fumarate. propionate. 522.88 Sterile amoxicillin trihydrate for sus- 522.850 Estradiol valerate and norgestomet pension. in combination. 522.90 Ampicillin implantation and 522.863 Ethylisobutrazine hydrochloride in- injectible dosage forms. jection. 522.90a Ampicillin trihydrate sterile suspen- 522.870 Etodolac. sion. 522.883 Etorphine hydrochloride injection. 522.900 Euthanasia solution. 522.90b Ampicillin trihydrate. 522.914 Fenprostalene solution. 522.90c Ampicillin sodium. 522.930 Firocoxib. 522.144 Arsenamide sodium aqueous injec- 522.955 Florfenicol. tion. 522.956 Florfenicol and flunixin. 522.147 Atipamezole. 522.960 Flumethasone implantation or 522.150 Azaperone. injectable dosage forms. 522.161 Betamethasone acetate and 522.960a Flumethasone suspension. betamethasone disodium phosphate aque- 522.960b Flumethasone acetate injection. ous suspension. 522.960c Flumethasone solution. 522.163 Betamethasone dipropionate and 522.970 Flunixin. betamethasone sodium phosphate aque- 522.995 Fluprostenol sodium injection. ous suspension. 522.1002 Follicle stimulating hormone. 522.204 Boldenone. 522.1004 Fomepizole. 522.234 Butamisole hydrochloride. 522.1010 Furosemide.
    [Show full text]
  • IV Induction Agents
    Intravenous drugs used for the induction of anaesthesia Dr Tom Lupton, Specialist Registrar in Anaesthesia Dr Oliver Pratt, Consultant Anaesthetist Salford Royal Hospitals NHS Foundation Trust, Salford, UK Key questions This tutorial reviews the basic pharmacology of common intravenous (IV) anaesthetic drugs. By the end of the tutorial, you should be able to decide on the most appropriate drug to use in the situations below and for what reason: 1. A patient with intestinal obstruction requires an emergency laparotomy. 2. A patient with a history of throat cancer, showing marked stridor and signs of respiratory distress, requires a tracheostomy. 3. A patient requiring a burn dressing change. 4. A patient with a history of heart failure requires a general anaesthetic. 5. A dehydrated hypovolaemic patient requires an emergency general anaesthetic. 6. A patient with porphyria comes for an inguinal hernia repair and is requesting a general anaesthetic. 7. A patient requires sedation on the intensive care unit. 8. Anaesthesia in the prehospital environment. What are IV induction drugs? These are drugs that, when given intravenously in an appropriate dose, cause a rapid loss of consciousness. This is often described as occurring within “one arm-brain circulation time” that is simply the time taken for the drug to travel from the site of injection (usually the arm) to the brain, where they have their effect. They are used: • To induce anaesthesia prior to other drugs being given to maintain anaesthesia. • As the sole drug for short procedures. • To maintain anaesthesia for longer procedures by intravenous infusion. • To provide sedation. The concept of intravenous anaesthesia was born in 1932, when Wesse and Schrapff published their report into the use of hexobarbitone, the first rapidly acting intravenous drug.
    [Show full text]
  • G/LIC/N/3/VEN/1 27 May 2002 ORGANIZATION (02-2903)
    WORLD TRADE G/LIC/N/3/VEN/1 27 May 2002 ORGANIZATION (02-2903) Committee on Import Licensing Original: Spanish AGREEMENT ON IMPORT LICENSING PROCEDURES1 Notification under Article 7.3 of the Agreement VENEZUELA The following communication, dated 16 May 2002, has been received from the Permanent Mission of the Bolivarian Republic of Venezuela. _______________ I. ADMINISTRATION OF TARIFF QUOTAS FOR A SERIES OF AGRICULTURAL ITEMS......................................................................................................1 II. IMPORT LICENCES FOR ENVIRONMENTAL PROTECTION PURPOSES ..............5 III. IMPORT LICENCES FOR PUBLIC HEALTH PURPOSES .............................................7 IV. IMPORT LICENCES FOR STATE SECURITY PURPOSES..........................................10 V. IMPORT LICENCES FOR SLOT MACHINES, ACCESSORIES AND EQUIPMENT..........................................................................................................................12 VI. IMPORT LICENCES FOR NEW SCRAPS FROM THE CLOTHING INDUSTRY..............................................................................................................................14 ANNEX 12 .............................................................................................................................................16 I. ADMINISTRATION OF TARIFF QUOTAS FOR A SERIES OF AGRICULTURAL ITEMS Outline of systems 1. System of administration of tariff quotas for a series of agricultural items, in accordance with the minimum access commitments made by Venezuela
    [Show full text]
  • 218 Part 522—Implantation Or Injectable Dosage Form
    Pt. 522 21 CFR Ch. I (4–1–07 Edition) by Mycoplasma gallisepticum sensitive 522.82 Aminopropazine fumarate sterile so- to tylosin. lution injection. (iii) Limitations. Do not use in layers 522.84 Beta-aminopropionitrile fumarate. 522.88 Sterile amoxicillin trihydrate for sus- producing eggs for human consump- pension. tion; administer from 2 to 5 days as 522.90 Ampicillin implantation and sole source of drinking water; treated injectible dosage forms. turkeys should consume enough medi- 522.90a Ampicillin trihydrate sterile suspen- cated drinking water to provide 60 mil- sion. ligrams of tylosin per pound of body 522.90b Ampicillin trihydrate for sterile sus- weight per day; prepare a fresh solu- pension. tion every 3 days; when sinus swelling 522.90c Ampicillin sodium for aqueous injec- tion. is present, inject the sinus with tylosin 522.144 Arsenamide sodium aqueous injec- injectable simultaneously with the tion. drinking water treatment; do not ad- 522.147 Atipamezole. minister within 5 days of slaughter. 522.150 Azaperone injection. (3) Swine—(i) Amount. 0.25 gram per 522.161 Betamethasone acetate and gallon. betamethasone disodium phosphate aque- (ii) Indications for use. For the control ous suspension. 522.163 Betamethasone dipropionate and and treatment of swine dysentery betamethasone sodium phosphate aque- (bloody scours) caused by pathogens ous suspension. sensitive to tylosin. 522.204 Boldenone. (iii) Limitations. As only source of 522.234 Butamisole hydrochloride. drinking water for 3 to 10 days, depend- 522.246 Butorphanol tartrate injection. ing on the severity of the condition 522.275 N-Butylscopolammonium bromide. being treated: mix fresh solution daily; 522.311 Carfentanil citrate injection.
    [Show full text]
  • Pharmacology Cito
    Pharmacology Cito 5 Read: it is important! Dear future physicians and pharmaceutists! The scientific and pedagogical staff of the Pharmacology department of the National University of Pharmacy (Kharkiv) presents a new textbook "Pharmacology – Cito!" to you. We want to change the myth that it is impossible to learn pharmacology quickly and qualitatively. The textbook "Pharmacology – Cito!" is published for those, who have decided to connect his or her profession with medicines, but think that a great amount of the information in pharmacology is hard to learn. Taking this fact into account we have decided to help those, who wish to master pharmacology in logical, fast - "Cito!"- version. Not be afraid of pharmacology! The 40-year experience of teaching pharmacology testifies that for the last 10-15 years a tendency of reducing the amount of classroom hours in pharmacology because of increasing the amount of the individual work is being observed. However, because of the lack of time and the constant increasing volume of information in pharmacology, everyone has not enough time to master it soundly and qualitatively. This textbook trains future pharmaceutists and physicians in the pharmacological logic, i.e. knowing the mechanisms of drug action one can understand their pharmacodynamics, naturally, on the basis of pharmacodynamics one can find logically the indications to their application and from their side effects the contraindications can be seen. The information about the peculiarities of medicines has been generalized and given as a pharmacological ―face‖ in tables. The volume of this textbook in pharmacology is sufficient for acquiring the confidence in the opportunity of the further improving of knowledge in this discipline, which is important for a physician and a pharmaceutist.
    [Show full text]
  • Lethal Injection Drug Access Could Put Executions on Hold Pentobarbital, Now Most-Commonly Used Execution Drug, Likely to Face Barriers in Coming Months
    Health Lethal injection drug access could put executions on hold Pentobarbital, now most-commonly used execution drug, likely to face barriers in coming months By Kimberly Leonard 6:00 am, April 4, 2012 Updated: 12:19 pm, May 19, 2014 Inmates on death row in the United States are executed by means of lethal injection. Dave Martin/AP 55 tweets Comment E-mail Print A federal judge’s decision to block imports of a drug used in executions will leave states to rely more on a substitute drug that could itself be getting scarce — developments that raise questions about both how these drugs are regulated and whether states will have the drugs they need to continue capital punishment by lethal injection. Over the past three decades, lethal injection has become the primary method of execution in the United States because it is widely viewed as the most humane alternative. Thirty-five states and the federal government use this method and more than 1,100 inmates have been put to death by lethal injection. State justice or corrections departments have conducted these executions by administering the anesthetic sodium thiopental in a lethal dosage on its own, or as part of a three-step “cocktail” in which sodium thiopental is followed by pancuronium bromide, a paralytic agent, then potassium chloride, which stops the heart and causes death. But in late March, a federal judge blocked importation of sodium thiopental, ruling that the Food and Drug Administration (FDA) ignored the law by allowing it to be imported into the country without following regulatory protocol.
    [Show full text]
  • Differential Effects of Halothane and Thiopental on Surfactant Protein C
    805 Anesthesiology 2000; 93:805–10 © 2000 American Society of Anesthesiologists, Inc. Lippincott Williams & Wilkins, Inc. Differential Effects of Halothane and Thiopental on Surfactant Protein C Messenger RNA In Vivo and In Vitro in Rats Catherine Paugam-Burtz, M.D.,* Serge Molliex, M.D, Ph.D.,† Bernard Lardeux, Ph.D.,‡ Corinne Rolland, T.A.,§, Michel Aubier, M.D,ʈ Jean-Marie Desmonts, M.D.,# Bruno Crestani, M.D., Ph.D.** Downloaded from http://pubs.asahq.org/anesthesiology/article-pdf/93/3/805/401255/0000542-200009000-00030.pdf by guest on 28 September 2021 Background: Pulmonary surfactant is a complex mixture of lung SP-C mRNA content to 53% of the value obtained in control proteins and phospholipids synthetized by alveolar type II (nonanesthetized, nonventilated) animals; thiopental anesthe- cells. Volatile anesthetics have been shown to reduce surfactant sia increased to 150% the lung SP-C mRNA content. phospholipid biosynthesis by rat alveolar type II cells. Surfac- Conclusions: These findings indicate that halothane and thio- tant-associated protein C (SP-C) is critical for the alveolar sur- pental used at clinically relevant concentrations modulate the factant functions. Our goal was to evaluate the effects of halo- pulmonary SP-C mRNA content in rats. In vivo, the additive role thane and thiopental on SP-C messenger RNA (mRNA) of mechanical ventilation is suggested. (Key words: Lung; pneu- expression in vitro in rat alveolar type II cells and in vivo in mocytes, volatile anesthetics.) mechanically ventilated rats. Methods: In vitro, freshly isolated alveolar type II cells were exposed to halothane during 4 h (1, 2, 4%) and 8 h (1%), and to PULMONARY surfactant is a complex mixture of pro- thiopental during 4 h (10, 100 ␮M) and 8 h (100 ␮M).
    [Show full text]
  • Administrative Records, Texas Department of Criminal Justice
    Consistent with the terms of the Court’s May 22, 2017 scheduling order, the record has been redacted for all information that plaintiff, Texas Department of Criminal Justice (Texas), has identified as confidential. In addition, Defendants have also redacted information that the drug’s supplier and broker have separately advised the agency they consider confidential and private, as well as information the agency itself generally treats as confidential. This information has been redacted pending final FDA’s review of confidentiality claims, and our filing of the record with these redactions does not necessarily reflect our agreement with all of the claims of confidentiality Defendants have received. Defendants explicitly reserve the right to make an independent determination regarding the proper scope of redactions at a later time. Should we identify any of Texas’s redactions that are over-broad or otherwise improper, we will work with Texas’s counsel to revise the redactions in the record. MISCELLANEOUS FDA 568 DOCUMENT#: VERSION#: DIOP PROCEDURE ~L ORO-DIOP- 2.00 FOOD & DRUG ADMINISTRATION .008 I OFFICE OF REGULATORY AFFAIRS PAGE 1 OF 4 TITLE: EFFECTIVE DATE: PROCESSING OF SODIUM THIOPENTAL ENTRIES 4/16/2012 Sections included in this document 1. Purpose 2. Scope 3. Responsibility 4. Background 5. References 6. Procedure 7. Definitions/Glossary 8. Records 9. Supporting Documents 10. Contact Information 11.Attachments Document History and Change History 1. Purpose Pending litigation, this procedure provides instructions on the handling of shipments of Sodium Thiopental by Districts and the responsibility of DIOP in the processing of Sodium Thiopental entries. Districts should disseminate this information to all pertinent staff handling these entries.
    [Show full text]
  • ANESTHESIA and ANALGESIA in LABORATORY ANIMALS, 2ND EDITION Copyright © 2008, 1997 by Elsevier Inc
    Anesthesia and Analgesia in Laboratory Animals AMERICAN COLLEGE OF LABORATORY ANIMAL MEDICINE SERIES Steven H. Weisbroth, Ronald E. Flatt, and Alan L. Kraus, eds.: The Biology of the Laboratory Rabbit, 1974 Joseph E. Wagner, and Patrick J. Manning, eds.: The Biology of the Guinea Pig, 1976 Edwin J. Andrews, Billy C. Ward, and Norman H. Altman, eds.: Spontaneous Animal Models of Human Disease, volume 1, 1979 Edwin J. Andrews, Billy C. Ward, and Norman H. Altman, eds.: Spontaneous Animal Models of Human Disease, volume 2, 1980 Henry J. Baker, J. Russell Lindsey, and Steven H. Weisbroth, eds.: The Laboratory Rat, Volume I: Biology and Diseases, 1979; Volume II: Research Applications, 1980 Henry L. Foster, J. David Small, and James G. Fox, eds.: The Mouse in Biomedical Research, Volume I: History, Genetics and Wild Mice, 1981, Volume II: Diseases, 1982; Vol. III: Normative Biology, Immunology and Husbandry, 1983; Vol. IV: Experimental Biology and Oncology, 1982 James G. Fox, Bennett J. Cohen, and Franklin M. Loew, eds.: Laboratory Animal Medicine, 1984 G.L. Van Hoosier, Jr., and Charles W. McPherson, eds.: Laboratory Hamsters, 1987 Patrick J. Manning, Daniel H. Ringler, and Christian E. Newcomer, eds.: The Biology of the Laboratory Rabbit, second edition, 1994 B. Taylor Bennett, Christian R. Abee, Roy Henrickson, eds: Nonhuman Primates in Biomedical Research, Biology and Management, 1995 Dennis F. Kohn, Sally K. Wixson, William J. White, and G. John Benson, eds.: Anesthesia and Analgesia in Laboratory Animals, 1997 B. Taylor Bennett, Christian R. Abee, Roy Henrickson, eds: Nonhuman Primates in Biomedical Research, Diseases, 1998 James G. Fox, Lynn C.
    [Show full text]