Bromides Potassium Bromide, Sodium Bromide Kbr and Nabr Are Other Names for This Medication
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What's the Best First Line Anticonvulsant?
What’s the best first line anticonvulsant? Stephen Hanson, DVM, MS, Dip. ACVIM (Neurology) Recurring seizure activity is a relatively common problem in canine patients. Nowadays, there are several good options for medical treatment, which makes the choice of which drug to use a little more complicated. All anticonvulsant drugs have advantages and disadvantages, so the selection of a first-line drug should be tailored for the individual patient and client. Phenobarbital: This has been the standard first choice drug for decades. The nice thing about Phenobarbital is that it works fairly well, controlling seizures in about 70% of dogs with epilepsy. Also, it is inexpensive and readily available. The biggest down-sides are its induction of hepatic metabolism and the need for frequent upward dose adjustments, as well as its potential to cause hepatotoxicity. The potential for liver disease increases with time, so a 2 year old dog placed on this medication is more likely to develop hepatotoxicity in his life-time than a 10 year old dog. Phenobarbital can also cause sedation and ataxia. While this is usually mild/transient, it can be a real problem in dogs with other pre- existing signs of intracranial disease. Polyuria, polydipsia and polyphagia are other common side effects. These signs vary widely in severity between patients. Pros: cheap, available at any corner pharmacy, works well Cons: higher doses required with time, possible serious liver side-effects Good first-line choice for middle-aged to older dogs without any pre-existing liver issues Poor choice for dogs with liver disease, dogs with other intracranial signs Questionable choice for young epileptic dogs Potassium/sodium bromide: This was the most commonly-used add on anticonvulsant drug for a long time. -
Nietzsche and Psychedelics – Peter Sjöstedt-H –
Antichrist Psychonaut: Nietzsche and Psychedelics – Peter Sjöstedt-H – ‘… And close your eyes with holy dread, For he on honey-dew hath fed, And drunk the milk of Paradise.’ So ends the famous fragment of Kubla Khan by the Romantic poet, Samuel Taylor Coleridge. He tells us that the poem was an immediate transcription of an opium-induced dream he experienced in 1797. As is known, the Romantic poets and their kin were inspired by the use of psychoactive substances such as opium, the old world’s common pain reliever. Pain elimination is its negative advantage, but its positive attribute lies in the psychedelic (‘mind- revealing’)1 state it can engender – a state described no better than by the original English opium eater himself, Thomas De Quincey: O just and righteous opium! … thou bildest upon the bosom of darkness, out of the fantastic imagery of the brain, cities and temples, beyond the art of Phidias and Praxiteles – beyond the splendours of Babylon and Hekatómpylos; and, “from the anarchy of dreaming sleep,” callest into sunny light the faces of long-buried beauties … thou hast the keys of Paradise, O just, subtle, and mighty opium!2 Two decades following the publication of these words the First Opium War commences (1839) in which China is martially punished for trying to hinder the British trade of opium to the Chinese people. Though opium, derived from the innocent garden poppy Papavar somniferum, may cradle the keys to Paradise it also clutches the keys to Perdition: its addictive thus potentially ruinous nature is commonly known. Today, partly for these reasons, opiates are mostly illegal without license – stringently so in their most potent forms of morphine and heroin. -
Comparison of Intranasal Versus Intravenous Midazolam for Management of Status Epilepticus in Dogs: a Multi-Center Randomized Parallel Group Clinical Study
Received: 16 July 2019 Accepted: 9 September 2019 DOI: 10.1111/jvim.15627 STANDARD ARTICLE Comparison of intranasal versus intravenous midazolam for management of status epilepticus in dogs: A multi-center randomized parallel group clinical study Marios Charalambous1 | Holger A. Volk2 | Andrea Tipold2 | Johannes Erath2 | Enrice Huenerfauth2 | Antonella Gallucci3 | Gualtiero Gandini3 | Daisuke Hasegawa4 | Theresa Pancotto5 | John H. Rossmeisl5 | Simon Platt6 | Luisa De Risio7 | Joan R. Coates8 | Mihai Musteata9 | Federica Tirrito10 | Francesca Cozzi10 | Laura Porcarelli11 | Daniele Corlazzoli11 | Rodolfo Cappello12 | An Vanhaesebrouck13 | Bart J.G. Broeckx14 | Luc Van Ham1 | Sofie F.M. Bhatti1 1Small Animal Department, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium 2Department of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Hannover, Germany 3Department of Veterinary Medical Sciences, University of Bologna, Bologna, Italy 4Department of Clinical Veterinary Medicine, Nippon Veterinary and Life Science University, Tokyo, Japan 5Department of Small Animal Clinical Sciences, Virginia-Maryland College of Veterinary Medicine, Blacksburg, Virginia 6Department of Small Animal Medicine and Surgery, College of Veterinary Medicine, University of Georgia, Athens, Georgia 7Small Animal Referral Centre, Animal Health Trust, Newmarket, United Kingdom 8Department of Veterinary Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia, Missouri 9Department of Clinical Veterinary -
Rectal Absorption in Childhood
RECTAL ABSORPTION IN CHILDHOOD by JOHN WILLIAM ALEXANDER MACKENZIE, M.B., Ch. THESIS SUBMITTED FOR DEGREE OF M.D. UNIVERSITY OF GLASGOW ProQuest Number: 13849818 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 13849818 Published by ProQuest LLC(2019). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States C ode Microform Edition © ProQuest LLC. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106- 1346 (i) CONTENTS Page Preface, ..« «». ••• ••• (ii) Introduction, ... ... ... 1. The Origins of Rectal Therapy, ... 1. The Present Position, ... ... 6. Investigation: A. The Absorption of Glucose, ... 11. Blood Sugar Studies, ... ... 15. The Glucose Content of the Rectal Washout. 18. The Effect of the Glucose Enema on Nitrogen Metabolism, ... ... 19. B. The Absorption of Sodium Chloride, ... 35. C. The Absorption of Predigested Protein, 41. D. The Absorption of Drugs, ... ... 53. 1. Potassium Bromide, ... ... 55. 2. Sodium Salicylate, ... ... 58. 3. Sulphanilamide, ... ... 65. Discussion. The Range of Substances Absorbed, ... 73. The Path of Absorption, ... ... 76. The Quantity Given, ... ... 80. General Conclusion, ... ... ... 84. General Summary, ... ... ... 86. APPENDIX. 1. Solutions used for Rectal Infusion, 87. 2. Biochemical Methods, ... 89. 3. Bibliography, ... ... 94. (ii) PREFACE The work for this thesis was carried out in the wards and biochemical laboratory of the Royal Hospital for Sick Children, Glasgow. -
Canine Status Epilepticus Care
Vet Times The website for the veterinary profession https://www.vettimes.co.uk CANINE STATUS EPILEPTICUS CARE Author : Stefano Cortellini, Luisa de Risio Categories : Vets Date : August 2, 2010 Stefano Cortellini and Luisa de Risio discuss emergency management techniques for a condition that can claim the lives of 25 per cent of afflicted dogs – as the quicker the start of treatment, the better the chances of control STATUS epilepticus (SE) is a neurological emergency with a mortality of up to 25 per cent in dogs (Bateman, 1999). SE can be defined as continuous epileptic seizure (ES) activity lasting longer than five minutes, or as two or more ES with incomplete recovery of consciousness interictally. SE has also been defined as continuous seizure activity lasting for 30 minutes or longer. However, emergency treatment to stop the ES should be administered well before the defined 30-minute time. The most common type of SE is generalised tonic-clonic status. When this is prolonged, the tonic- clonic clinical manifestations can become subtle, with only small muscle twitching and altered mentation. This status is called electromechanical dissociation, as continued abnormal electrical activity in the brain persists while the motor manifestations are minimal to absent. In these cases, emergency anti-epileptic treatment is necessary as for tonic-clonic status. SE can be divided into two stages. The first stage is characterised by generalised tonicclonic seizures and an increase in autonomic activity that causes tachycardia, hypertension, 1 / 7 hyperglycaemia, hyperthermia and increased cerebral blood flow. The second stage of SE starts after about 30 minutes and is characterised by hypotension, hypoglycaemia, hyperthermia, hypoxia, decreased cerebral blood flow, cerebral oedema and increased intracranial pressure. -
Determination of Bromine Number According ASTM D 1159
SI Analytics-Application report Titration Determination of bromine number according ASTM D 1159 Description This application note describes the determination of the bromine number of petroleum distillates, olefins and similar samples with a bromine number > 1. For bromine numbers < 1 please use the test method for ASTM D 2710 or for aromatic hydrocarbons the coulometric test method ASTM D1492. Instruments Titrator TL 7000 or higher with 10 or 20 ml burette. Electrode Pt 1200, Pt 1400 or KF 1100 and temperature sensor (e.g. W W 5790 NN) Cable L 1 NN (only for Pt 1200 and Pt 1400) Stirrer Magnetic stirrer TM 235 Lab accessory Glass beaker 150 ml or larger with an ice bath or double jacketed titration vessel TZ 1756 with a cryostat. The sample have to be maintained at a temperature between 0 – 5 °C. 50 ml volumetric flask with stopper, 250 ml graduated measuring cylinder 5 ml volumetric pipette or variable one Magnetic stirrer bar 30 mm Reagents 1 Bromide-Bromate, Standard Solution(0.2500 M as Br2) 2 Glacial acetic acid 3 Dichloromethane (as replacement of 1,1,1-trichloroethane) 4 Methanol 5 Sodium thiosulfate solution 0.1 M for standardization of the titrant (optional) 7 Sulfuric acid 1/5 diluted (1 part H2SO4 conc. + 5 parts water) 6 Potassium Iodide solution (150 g/L) for standardization of the titrant (optional) 8 Starch indicator solution of redox electrode Pt 62 (+ WA 50 exchangeable unit) All reagents should be of analytical grade or better. Bromine number ASTM D 1159.docx 1/4 Titration procedure Titration solvent Prepare 1 L of titration solvent by mixing the following volumes of materials: 714 mL of glacial acetic acid, 134 mL of 1,1,1-trichloroethane (or better dichloromethane), 134 mL of methanol, and 18 mL of H2SO4(1 + 5). -
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WORLD HEALTH ORGANIZATION MNH/83.7 ORGANISATION MONDIALE D! LA SANTE ..' ,I ORIGINAL: ENGLISH/ t) I'(.AA ... ) ' -I r:r, t......J5.--iA. rl V{. rICI-..... l... FRENCH {\~ ' l ~' , C, .. {.;'.; (,( 0 ' . \"'''-C:.. ~\ ~ ~v '- ' / '~ v- J C; SEVENTH REVIEW OF PSYCHOACTIVE SUBSTANCES FOR INTERNATIONAL CONTROL ) Geneva, 7-11 March 1983 " : CONTENTS INDEXED _, INTRODUCTION 1 SCOPE OF THE MEETING • 2 SOURCES AND NATURE OF DATA REVIEWED 2 REVIEW OF DRUGS FOR INTERNATIONAL CONTROL 2 i 4.1 Alfentanil 2 . 4.2 Chloral hydrate • 3 :4.3 Paraldehyde • • • 3 4.4 Potassium bromide 3 ' 4.5 Buprenorphine 3 ,4.6 Butorphanol • 4 4.7 Cyclazocine 4 4.8 Nalbuphine 4 4.9 Pentazocine • • • • 4 WHO'S CANCER PAIN RELIEF PROGRAMME 5 .; CONSIDERATIONS OF FUTURE PROGRAMMES • • • • 5 LIST OF PARTICIPANTS 6 ~~ EX I ...... 8 INTRODUCTION Dr Halfdan Mahler, Director-General of WHO, Dr Lu Rushan, Assistant tor-General of WHO, welcomed the participants in this meeting and expressed the concern of Tegarding the process of reviewing substances for international control. Dr Norman Sartorius, Director, Division of Mental Health WHO, discussed with the ipants the conditions in the developing nations which must be considered in reaching regarding the recommendation of substances for international control. He referred ifically to a gradual change in the attitude of people towards pain. No longer is pain as a natural accompaniment of disease. The effective analgesics, widely available the developed countries of the world, must become available for legitimate medical needs P~ tients in the developing countries. This availability of analgesic drugs must however into account the fact that many such substances are capable of producing dependence and • consequence significant public health and social problems. -
Studies on Isotope Separation of Lithium by Electromigration in Fused Lithium Bromide and Potassium Bromide Mixture, (II) Composition of Salt in Anode Compartment
Journal of NUCLEARSCIENCE and TECHNOLOGY,7 (10), p. 522~526 (October 1970). Studies on Isotope Separation of Lithium by Electromigration in Fused Lithium Bromide and Potassium Bromide Mixture, (II) Composition of Salt in Anode Compartment Yoshinobu YAMAMURA* and Shin SUZUKI* Received May 13, 1970 Accurate knowledge on the salt composition in the anode compartment is indispensable when 6Li is to be highly enriched by electromigration in fused LiBr-KBr mixture. A study was made on the dependence on temperature shown by the salt composition in the anode com- partment. It was observed that sustained electromigration led to a salt composition in the anode compartment that was determined by the prevailing temperature. The composition was observed for various temperatures between 380- and 740-C: In terms of the ratio Li/K in chemical equivalent, the values were 1.31 at 380-C, 1.29 at 420-C, 1.31 at 460-C, 1.41 at 500-C, 1.76 at 540-C, 1.82 at 580-C, 1.95 at 620-C, 2.16 at 680-C and 2.34 at 740-C. These results can be explained by assuming that the fused LiBr-KBr mixture is a system composed of two simple salts and their eutectic, and that at temperatures below 550-C, which is the melting point of LiBr, LiBr and KBr are dissolved in fused eutectic, while KBr is dissolved in the fused eutectic and LiBr at temperatures between 550- and 738-C, which latter is the melting point of KBr. I. INTRODUCTION . EXPERIMENTAL In a previous study(1), one of authors suc- 1. -
186.Full.Pdf
186 CHEMISTR Y: BA NCROFT AND R UTZLER. JR. PROC. N. A. S. I This work is part of the programme now being carried out at Cornell University under a grant from the Heckscher Foundation for the Advancement of Research estab- lished by August Heckscher at Cornell University. 2 Holleman, Rec. trav. chim., 24, 140 (1905). 3 Holleman, Ibid., 23, 225 (1904). 4Drogin and Rosanoff, J. Am. Chem. Soc., 38, 711 (1916). 5 Kraay, Rec. trav. chim., 48, 1055 (1929). 6 De Grauw, Ibid., 48, 1061 (1929). RE VERSIBLE COAGULA TION IN LIVING TISSUE. II By WILDER D. BANCROFTr AND J. E. RUTZLER, JR.2 BAKER CHEMICAL LABORATORY, CORNELL UNIVERSITY Communicated March 3, 1931 Since relief from the addiction to drugs is one of the important problems of the civilized world, it seems wise to see what the outcome is from the application of Claude Bernard's theory of anesthesia to morphinism. Gwathmey' says: "The ganglion cell, according to Binz, is the point of attack of the anesthetic agent. In his experiments, fresh sections of the brain cortex of rabbits were placed in a one per cent solution of morphine hydrochloride, or exposed to chlorine vapors. The effect of coagulation- necrosis was produced, as is seen when protoplasmic poisons of neutral reaction are allowed to act upon large transparent infusoria. The proto- plasm is first darkened, and the movements become sluggish; later the protoplasm becomes granulated, and the movements cease. Recupera- tion may take place from the first stage by washing away the poisons [it can be seen that this is the same as the peptization of gels by washing out the coagulating agent]; but not from the last stage. -
Pharmaceuticals and Medical Devices Safety Information No
Pharmaceuticals and Medical Devices Safety Information No. 260 August 2009 Table of Contents 1. Tricyclic and tetracyclic antidepressants, associated with aggression ................................................................................................... 3 2. Important Safety Information .................................................................. 9 .1. Telmisartan ··························································································· 9 .2. Phenytoin, Phenytoin/Phenobarbital, Phenytoin/Phenobarbital/ Caffeine and Sodium Benzoate, Phenytoin Sodium ··························· 13 3. Revision of PRECAUTIONS (No. 208) Lamotrigine (and 9 others) ············································································ 17 4. List of products subject to Early Post-marketing Phase Vigilance ..................................................... 21 This Pharmaceuticals and Medical Devices Safety Information (PMDSI) is issued based on safety information collected by the Ministry of Health, Labour and Welfare. It is intended to facilitate safer use of pharmaceuticals and medical devices by healthcare providers. PMDSI is available on the Pharmaceuticals and Medical Devices Agency website (http://www.pmda.go.jp/english/index.html) and on the MHLW website (http://www.mhlw.go.jp/, Japanese only). Published by Translated by Pharmaceutical and Food Safety Bureau, Pharmaceuticals and Medical Devices Agency Ministry of Health, Labour and Welfare Pharmaceutical and Food Safety Bureau, Office of Safety I, Ministry of -
LIST of PRODUCTS BULK DRUGS Sl. No Name of the Product Production TPM 1. Carvedilol Phosphate 2.50 2. Citalopram Hydrobromide 10
LIST OF PRODUCTS BULK DRUGS Sl. No Name of the product Production TPM 1. Carvedilol phosphate 2.50 2. Citalopram Hydrobromide 10.00 3. Closantel sodium 5.00 4. Esomeprazole magnesium trihydrate 1.50 5. Fexofinadine hydrochloride 2.00 6. Fosfomycin trometamol 3.00 7. Gaba-pentin 3.00 8. Itraconozole 2.00 9. Lansoprazole 3.00 10. Lornoxicam 4.00 11. Montelukast sodium 3.00 12. Omeprazole 5.00 13. Ondansetron 3.00 14. Oxyclozanide 5.00 15. Ritonavir 3.00 16. Rosuvastatin calcium 3.00 17. Setraline hydrochloride 2.00 18. Sparfloxacin 2.00 19. Terbinafine hydrochloride 3.00 Total 65.00 INTERMEDIATES Sl. No Name of the product Production TPM 1 Tri Chloro Salisylic Acid 3.00 2 5-AminO-2-Hydroxy Benzoic acid 2.00 3 5-Amino-2-dibenzylamino-1,6-diphenyl-hex-4-en-3-one 2.00 4 2-Amino-6-chloro-3-nitro pyridine 3.00 5 4-Chloro butyryl chloride 3.00 CHEMICALS Sl.No Name of the product Production TPM 1 Tributyl Tin chloride 90 2 L-Menthol 90 3 Dicyclo Hexylcarbomidiimide 90 SOLVENT RECOVERY Sl.No Name of the product Production TPM 1 All solvents 450 Industry proposes to produce • 2.0 TPD either from bulk drug group or intermediate group • 3.0 TPD from chemicals group • 15.0 TPD solvent recovery CARVEDILOL PHOSPHATE Carvedilol Phosphate can be manufactured in four stages. Stage-1: 1-(2-bromo ethoxy)-2-methoxy benzene and benzyl amine reacts together in the presence of toluene solvent medium forms stage-1 compound. O Toluene Br + NH2 O 1-(2-Bromo-ethoxy)- 2-methoxy-benzene Benzylamine C9H11BrO2 C7H9N Mol. -
The Preparation, Characterization, and Thermal Decomposition Products Op Di-Tkrtiaky Butyl Carbonate and Tertiary Butyl Chlorocahbonate
Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1948 The rP eparation, Characterization, and Thermal Decomposition Products of Di-Tertiary Butyl- Carbonate and Tertiary Butyl-Chlorocarbonate. James Wesley Rogers Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Part of the Chemistry Commons Recommended Citation Rogers, James Wesley, "The rP eparation, Characterization, and Thermal Decomposition Products of Di-Tertiary Butyl-Carbonate and Tertiary Butyl-Chlorocarbonate." (1948). LSU Historical Dissertations and Theses. 7911. https://digitalcommons.lsu.edu/gradschool_disstheses/7911 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. MANUSCRIPT THESES Unpublished theses submitted for the master's and doctor's degrees and deposited in the Louisiana State University Library are available for inspection* Use of any thesis is limited by the rights of the author* Bibliographical references may be noted* but passages may not be copied unless the author has given permission# Credit rnust be given in subsequent written or published work# A library which borrows this thesis for use by its clientele is expected to make sure that the borrower is aware of