Gender Differences in Psychotropic Medicine Dispensing at a Pharmacy
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Medicines Regulations 1984 (SR 1984/143)
Reprint as at 1 July 2014 Medicines Regulations 1984 (SR 1984/143) David Beattie, Governor-General Order in Council At the Government House at Wellington this 5th day of June 1984 Present: His Excellency the Governor-General in Council Pursuant to section 105 of the Medicines Act 1981, and, in the case of Part 3 of the regulations, to section 62 of that Act, His Excellency the Governor-General, acting on the advice of the Minister of Health tendered after consultation with the organisations and bodies that ap- peared to the Minister to be representatives of persons likely to be substantially affected, and by and with the advice and consent of the Executive Council, hereby makes the following regulations. Contents Page 1 Title and commencement 5 Note Changes authorised by subpart 2 of Part 2 of the Legislation Act 2012 have been made in this official reprint. Note 4 at the end of this reprint provides a list of the amendments incorporated. These regulations are administered by the Ministry of Health. 1 Reprinted as at Medicines Regulations 1984 1 July 2014 2 Interpretation 5 Part 1 Classification of medicines 3 Classification of medicines 11 Part 2 Standards 4 Standards for medicines, related products, medical 11 devices, cosmetics, and surgical dressings 5 Pharmacist may dilute medicine in particular case 12 6 Colouring substances [Revoked] 12 Part 3 Advertisements 7 Advertisements not to claim official approval 13 8 Advertisements for medicines 13 9 Advertisements for related products 15 10 Advertisements for medical devices 15 11 Advertisements -
(12) United States Patent (10) Patent No.: US 8,603,526 B2 Tygesen Et Al
USOO8603526B2 (12) United States Patent (10) Patent No.: US 8,603,526 B2 Tygesen et al. (45) Date of Patent: Dec. 10, 2013 (54) PHARMACEUTICAL COMPOSITIONS 2008. O152595 A1 6/2008 Emigh et al. RESISTANT TO ABUSE 2008. O166407 A1 7/2008 Shalaby et al. 2008/0299.199 A1 12/2008 Bar-Shalom et al. 2008/0311205 A1 12/2008 Habib et al. (75) Inventors: Peter Holm Tygesen, Smoerum (DK); 2009/0022790 A1 1/2009 Flath et al. Jan Martin Oevergaard, Frederikssund 2010/0203129 A1 8/2010 Andersen et al. (DK); Karsten Lindhardt, Haslev (DK); 2010/0204259 A1 8/2010 Tygesen et al. Louise Inoka Lyhne-versen, Gentofte 2010/0239667 A1 9/2010 Hemmingsen et al. (DK); Martin Rex Olsen, Holbaek 2010, O291205 A1 11/2010 Downie et al. (DK); Anne-Mette Haahr, Birkeroed 2011 O159100 A1 6/2011 Andersen et al. (DK); Jacob Aas Hoellund-Jensen, FOREIGN PATENT DOCUMENTS Frederikssund (DK); Pemille Kristine Hoeyrup Hemmingsen, Bagsvaerd DE 20 2006 014131 1, 2007 (DK) EP O435,726 8, 1991 EP O493513 7, 1992 EP O406315 11, 1992 (73) Assignee: Egalet Ltd., London (GB) EP 1213014 6, 2002 WO WO 89,09066 10, 1989 (*) Notice: Subject to any disclaimer, the term of this WO WO91,040 15 4f1991 patent is extended or adjusted under 35 WO WO95/22962 8, 1995 U.S.C. 154(b) by 489 days. WO WO99,51208 10, 1999 WO WOOOf 41704 T 2000 WO WO 03/024426 3, 2003 (21) Appl. No.: 12/701,429 WO WOO3,O24429 3, 2003 WO WOO3,O24430 3, 2003 (22) Filed: Feb. -
(12) United States Patent (10) Patent No.: US 9,005,660 B2 Tygesen Et Al
USOO9005660B2 (12) United States Patent (10) Patent No.: US 9,005,660 B2 Tygesen et al. (45) Date of Patent: Apr. 14, 2015 (54) IMMEDIATE RELEASE COMPOSITION 4,873,080 A 10, 1989 Bricklet al. RESISTANT TO ABUSEBY INTAKE OF 4,892,742 A 1, 1990 Shah 4,898,733. A 2f1990 DePrince et al. ALCOHOL 5,019,396 A 5/1991 Ayer et al. 5,068,112 A 11/1991 Samejima et al. (75) Inventors: Peter Holm Tygesen, Smoerum (DK); 5,082,655 A 1/1992 Snipes et al. Jan Martin Oevergaard, Frederikssund 5,102,668 A 4, 1992 Eichel et al. 5,213,808 A 5/1993 Bar Shalom et al. (DK); Joakim Oestman, Lomma (SE) 5,266,331 A 11/1993 Oshlack et al. 5,281,420 A 1/1994 Kelmet al. (73) Assignee: Egalet Ltd., London (GB) 5,352.455 A 10, 1994 Robertson 5,411,745 A 5/1995 Oshlack et al. (*) Notice: Subject to any disclaimer, the term of this 5,419,917 A 5/1995 Chen et al. patent is extended or adjusted under 35 5,422,123 A 6/1995 Conte et al. U.S.C. 154(b) by 473 days. 5,460,826 A 10, 1995 Merrill et al. 5,478,577 A 12/1995 Sackler et al. 5,508,042 A 4/1996 OShlack et al. (21) Appl. No.: 12/701.248 5,520,931 A 5/1996 Persson et al. 5,529,787 A 6/1996 Merrill et al. (22) Filed: Feb. 5, 2010 5,549,912 A 8, 1996 OShlack et al. -
Ehealth DSI [Ehdsi V2.2.2-OR] Ehealth DSI – Master Value Set
MTC eHealth DSI [eHDSI v2.2.2-OR] eHealth DSI – Master Value Set Catalogue Responsible : eHDSI Solution Provider PublishDate : Wed Nov 08 16:16:10 CET 2017 © eHealth DSI eHDSI Solution Provider v2.2.2-OR Wed Nov 08 16:16:10 CET 2017 Page 1 of 490 MTC Table of Contents epSOSActiveIngredient 4 epSOSAdministrativeGender 148 epSOSAdverseEventType 149 epSOSAllergenNoDrugs 150 epSOSBloodGroup 155 epSOSBloodPressure 156 epSOSCodeNoMedication 157 epSOSCodeProb 158 epSOSConfidentiality 159 epSOSCountry 160 epSOSDisplayLabel 167 epSOSDocumentCode 170 epSOSDoseForm 171 epSOSHealthcareProfessionalRoles 184 epSOSIllnessesandDisorders 186 epSOSLanguage 448 epSOSMedicalDevices 458 epSOSNullFavor 461 epSOSPackage 462 © eHealth DSI eHDSI Solution Provider v2.2.2-OR Wed Nov 08 16:16:10 CET 2017 Page 2 of 490 MTC epSOSPersonalRelationship 464 epSOSPregnancyInformation 466 epSOSProcedures 467 epSOSReactionAllergy 470 epSOSResolutionOutcome 472 epSOSRoleClass 473 epSOSRouteofAdministration 474 epSOSSections 477 epSOSSeverity 478 epSOSSocialHistory 479 epSOSStatusCode 480 epSOSSubstitutionCode 481 epSOSTelecomAddress 482 epSOSTimingEvent 483 epSOSUnits 484 epSOSUnknownInformation 487 epSOSVaccine 488 © eHealth DSI eHDSI Solution Provider v2.2.2-OR Wed Nov 08 16:16:10 CET 2017 Page 3 of 490 MTC epSOSActiveIngredient epSOSActiveIngredient Value Set ID 1.3.6.1.4.1.12559.11.10.1.3.1.42.24 TRANSLATIONS Code System ID Code System Version Concept Code Description (FSN) 2.16.840.1.113883.6.73 2017-01 A ALIMENTARY TRACT AND METABOLISM 2.16.840.1.113883.6.73 2017-01 -
Tranquillizing and Thymoleptic Drugs in Outpatient and General Practice
TRANQUILLIZING AND THYMOLEPTIC DRUGS IN OUTPATIENT AND GENERAL PRACTICE BY r R. E. HEMPHILL, M.A., M.D., D.P.M. Lecturer in Mental Health, University of Bristol, Consultant Psychiatrist, Glenside-Barrow and United Bristol Hospitals AND J. E. BARBER, M.B., CH.B., D.(OBST.)R.C.O.G. * Clinical Research Assistant, Barrow Hospital. An account of these drugs was published in this Journal in 1962 (Hemphill, 1962). The present paper is a revision of the earlier survey, and includes a review of the newer drugs and recent developments. For clarity, sections of the original paper have been quoted completely or in part. The numerous preparations are divided for convenience into tranquillizers, anti- depressants and an intermediate group. This classification is clinical, and does not necessarily imply that the drugs in one group have a similar chemical structure or pharmacological action. The effect of these drugs in the human is complex, and is not necessarily the same in the sick as in the mentally well. Anxious persons and those with autonomic instability are particularly sensitive to some, and may develop side effects at a low dosage, in contrast to the usual tolerance of schizophrenics and other psychotics. Since tranquillizers and thymoleptics influence mood and emotion, it is to be expected that they will have an effect on other functions which involve the autonomic nervous system. Control of blood pressure, of intestinal and bladder muscle, and secretion of saliva and alimentary juices, for example, may be interfered with. Hypotension and dry mouth are common side effects, and therapeutic doses of some of the drugs can cause retention of urine and ileus. -
(12) United States Patent (10) Patent No.: US 9,023,394 B2 Andersen Et Al
USOO9023394B2 (12) United States Patent (10) Patent No.: US 9,023,394 B2 Andersen et al. (45) Date of Patent: *May 5, 2015 (54) FORMULATIONS AND METHODS FOR THE 4,330,338 A 5, 1982 Banker CONTROLLED RELEASE OF ACTIVE DRUG 4.389,393 A 6, 1983 Schor et al. 4.404,183 A 9, 1983 Kawata et al. SUBSTANCES 4,449,983 A 5/1984 Cortese et al. 4,503,067 A 3, 1985 Wiedemann et al. (71) Applicant: Egalet Ltd., London (GB) 4,686,212 A 8, 1987 Ducatman et al. 4,824,675 A 4/1989 Wong et al. (72) Inventors: Christine Andersen, Vedbaek (DK); 4,844,984 A 7, 1989 Eckenhoffetal. 4,873,080 A 10, 1989 Bricklet al. Karsten Lindhardt, Haslev (DK); Jan 4,892,742 A 1, 1990 Shah Martin Oevergaard, Frederikssund 4,898,733. A 2f1990 DePrince et al. (DK); Louise Inoka Lyhne-versen, 5,019,396 A 5/1991 Ayer et al. Gentofte (DK); Martin Rex Olsen, 5,068,112 A 11/1991 Samejima et al. Holbaek (DK); Anne-Mette Haahr, 5,082,655 A 1/1992 Snipes et al. 5,102,668 A 4, 1992 Eichel et al. Birkeroed (DK); Pernille Kristine 5,213,808 A 5/1993 Bar Shalom et al. Hoeyrup Hemmingsen, Bagsvaerd 5,266,331 A 11/1993 Oshlack et al. (DK) 5,281,420 A 1/1994 Kelmet al. 5,352.455 A 10, 1994 Robertson (73) Assignee: Egalet Ltd., London (GB) 5,411,745 A 5/1995 Oshlack et al. 5,419,917 A 5/1995 Chen et al. -
Säädk 415/2019
SUOMEN SÄÄDÖSKOKOELMA MuuMnrovvvvLääkealanlääkeluettelosta asia turvallisuus- ja kehittämiskeskuksen päätös Julkaistu Helsingissä 29 päivänä maaliskuuta 2019 415/2019 Lääkealan turvallisuus- ja kehittämiskeskuksen päätös lääkeluettelosta Lääkealan turvallisuus- ja kehittämiskeskus on 10 päivänä huhtikuuta 1987 annetun lääkelain (395/1987) 83 §:n nojalla päättänyt vahvistaa seuraavan lääkeluettelon: 1§ Luettelon tarkoitus Tämä päätös sisältää luettelon Suomessa lääkkeellisessä käytössä olevista aineista ja rohdoksista. Lääkeluettelo laaditaan ottaen huomioon lääkelain 3 §:n ja 5 §:n säännökset. Lääkkeellä tarkoitetaan valmistetta tai ainetta, jonka tarkoituksena on sisäisesti tai ul- koisesti käytettynä parantaa, lievittää tai ehkäistä sairautta tai sen oireita ihmisessä tai eläi- messä. Lääkkeeksi katsotaan myös sisäisesti tai ulkoisesti käytettävä aine tai aineiden yh- distelmä, jota voidaan käyttää ihmisen tai eläimen elintoimintojen palauttamiseksi, kor- jaamiseksi tai muuttamiseksi farmakologisen, immunologisen tai metabolisen vaikutuk- sen avulla taikka terveydentilan tai sairauden syyn selvittämiseksi. Lääkeluettelo ei ole tyhjentävä. Tässä luettelossa mainitsemattomat aineet ja rohdokset, jotka täyttävät lääkelain lääkkeen määritelmän, ovat lääkkeitä. Lääkeluettelon vahvistamisen lisäksi Lääkealan turvallisuus- ja kehittämiskeskus päättää lääkelain 6 §:n nojalla tarvittaessa, onko ainetta tai valmistetta pidettävä lääkkeenä. Keskus päättää tapauskohtaisesti onko luettelossa olevaa ainetta sisältävää valmistetta pidettävä lääk- keenä -
Medicines Regulations 1984 (SR 1984/143)
Reprint as at 30 March 2021 Medicines Regulations 1984 (SR 1984/143) David Beattie, Governor-General Order in Council At the Government House at Wellington this 5th day of June 1984 Present: His Excellency the Governor-General in Council Pursuant to section 105 of the Medicines Act 1981, and, in the case of Part 3 of the regulations, to section 62 of that Act, His Excellency the Governor-General, acting on the advice of the Minister of Health tendered after consultation with the organisations and bodies that appeared to the Minister to be representatives of persons likely to be substantially affected, and by and with the advice and consent of the Executive Coun- cil, hereby makes the following regulations. Contents Page 1 Title and commencement 5 2 Interpretation 5 Part 1 Classification of medicines 3 Classification of medicines 9 Note Changes authorised by subpart 2 of Part 2 of the Legislation Act 2012 have been made in this official reprint. Note 4 at the end of this reprint provides a list of the amendments incorporated. These regulations are administered by the Ministry of Health. 1 Reprinted as at Medicines Regulations 1984 30 March 2021 Part 2 Standards 4 Standards for medicines, related products, medical devices, 10 cosmetics, and surgical dressings 4A Standard for CBD products 10 5 Pharmacist may dilute medicine in particular case 11 6 Colouring substances [Revoked] 11 Part 3 Advertisements 7 Advertisements not to claim official approval 11 8 Advertisements for medicines 11 9 Advertisements for related products 13 10 Advertisements -
Psychotropic Drugs G
Postgrad Med J: first published as 10.1136/pgmj.60.710.881 on 1 December 1984. Downloaded from Postgraduate Medical Journal (December 1984) 60, 881-885 Psychotropic drugs G. W. HANKS B.Sc., M.B., M.R.C.P. The Royal Marsden Hospital, Fulham Road, London SW3 6JJ Introduction system-depressant effect ofthese drugs: by depressing the general level of arousal the central perception of The interaction between the cognitive component pain may be modified. (the perception ofnociceptive, or painful stimuli) and In this review the evidence for intrinsic analgesic the affective component of pain is reflected in the activity and overlap between the actions of anti-nociceptive the place of psychotropic drugs in the agents (analgesics) and mood-altering drugs (psycho- treatment of chronic pain are discussed in the light of tropics) when treating pain patients. Anxiety, depres- the published literature and recent clinical experi- sion, fear and sleeplessness may all respond to ence. psychotropic drugs, and this may result in a reduc- tion in pain or a greater ability to cope with it. This TABLE 1. The WHO classification of psychotropic drugs may enable a patient's pain to be controlled with a Neuroleptics by copyright. smaller dose of analgesic. In this sense psychotropic Anxiolytic sedatives drugs have an 'analgesic' effect but it is a misleading Antidepressants use of the word, and has been the source of much Psychostimulants misunderstanding. Psychodysleptics In the day-to-day management of pain problems the two groups of drugs do have well-defined indications. Acute pain is invariably associated with Neuroleptics nociception, and responds to analgesics or other Neuroleptics are antipsychotic agents of which the antinociceptive treatments. -
Journal of Pharmacy and Pharmacology 1958 Volume.10 Suppl
The Journal of PHARMACY and PHARMACOLOGY Successor;sor to The Quarterly Journal o f Pharmacy and PharmacologyPharma 17 BLOOMSBURY SQUARE, LONDON, W.C.l Telephone: HOLborn 8967 Telegrams: Pharmakon, Westcent, London Editor: George Brownlee, D.Sc., Ph.D., F.P.S. Assistant Editor: J. R. Fowler, B.Pharm., F.P.S. CONTENTS BRITISH PHARMACEUTICAL CONFERENCE p a g e R eport o f Proceedings .......................................................................................... IT Chairman’s Address Modern Analytical Chemistry in the Service of Pharmacy and Medicine. By G. E. F o s t e r ..............................................................9 T Symposium E v a l u a t i o n o f N e w D r u g s . By L. G. Goodwin and F. L. Rose .. 24 T Science Papers and Discussions The Basis for “Sufficient of a Suitable Bacteriostatic” in Injec tions. By G. Sykes ..........................................................................40 T The Factors Influencing Sterilisation by Low Pressure Steam. Part I. Design and Instrumentation. By T. E. Barson, F. Peacock, E. L. Robins and G. R. Wilkinson .. .. .. .. .. 47 T The Factors Influencing Sterilisation by Low Pressure Steam. Part II. The Influence of Water Content of Cotton Gowns on Equilibrium Times. By T. E. Barson, F. Peacock, E. L. Robins and G. R. W ilk in s o n ..........................................................................56 T The Colorimetric D etermination of Morphine in G alenical Preparations. By C. A. Johnson and Cecilia J. Lloyd .. .. 60 T Some Observations Concerning the Chemical Reactions Occur ring Between Formaldehyde and Peptone. By Kenneth Bullock and V. Subba Rao .. .. .. .. .. .. 72 T The Effects of Added Peptone on the Bactericidal Action of Solutions of Formaldehyde. -
Qsar Study of Phenothiazines
STUDIA UBB CHEMIA, LXI, 1, 2016 (p. 305-316) (RECOMMENDED CITATION) Dedicated to Professor Mircea Diudea on the Occasion of His 65th Anniversary QSAR STUDY OF PHENOTHIAZINES ATENA PÎRVAN MOLDOVANa,*, SARA ERSALIa, RALUCA POPb ABSTRACT. A QSAR study on a set of 30 phenothiazines performed within a hypermolecule frame, to model their logP and LD50 values, is reported. The initial set of molecules was split into a training set and the test set; Cluj topological indices and some quantum mechanical descriptors have been used to derive the models, which were next tested for predictability by LOO, external validation and similarity clustering. Key words: phenothiazine, hypermolecule, LD50, logP, topological indices. INTRODUCTION Phenothiazine is an organic heterocyclic compound, of the class of thiazines, with the brute formula S(C6H4)2NH, of which skeleton occurs in various antipsychotic, antihistaminic, antiemetic, etc. drugs. Phenothiazine was synthesized by Bernthsen in 1883 by melting the diphenylamine with sulfur; its medicamentous derivatives are currently synthesized by the cyclization of substituted diphenylamines or diphenyl sulfides. Synthesis of methylene blue was reported in 1876 and is still used as antiseptic, antihelminthic drug. Phenothiazine antipsychotics, like chlorpromazine and prochlorperazine, are used to treat serious mental and emotional disorders, including schizophrenia and other psychotic disorders. Phenothiazine antipsychotics are classified into three groups, differing with respect to the substituent on nitrogen: the aliphatic compounds, piperidine compounds and piperazine derivatives. As antihistaminic, the promethazine is the most used phenothiazine. a Babeş-Bolyai University, Faculty of Chemistry and Chemical Engineering, 11 Arany Janos str., RO-400028, Cluj-Napoca, Romania b University of Medicine and Pharmacy “Victor Babes” Timisoara, Faculty of Pharmacy, E. -
TCI AMERICA Page 1 of 5 SAFETY DATA SHEET Revision Number: 1.1 Revision Date: 07/06/2018
TCI AMERICA Page 1 of 5 SAFETY DATA SHEET Revision number: 1.1 Revision date: 07/06/2018 1. IDENTIFICATION Product name: Apronal Product code: A2844 Product use: For laboratory research purposes. Restrictions on use: Not for drug or household use. Company: Emergency telephone number: TCI America Chemical Emergencies: 9211 N. Harborgate Street TCI America (8:00am - 5:00pm) PST Portland, OR 97203 U.S.A. +1-503-286-7624 Telephone: Transportation Emergencies: +1-800-423-8616 / +1-503-283-1681 Chemtrec 24-Hour Fax: +1-800-424-9300 (U.S.A.) +1-888-520-1075 / +1-503-283-1987 +1-703-527-3887 (International) e-mail: Responsible department: [email protected] TCI America www.TCIchemicals.com Environmental Health Safety and Security +1- 503-286-7624 2. HAZARD(S) IDENTIFICATION OSHA Haz Com: CFR 1910.1200: Acute Toxicity - Oral [Category 4] WHMIS 2015: Signal word: Warning! Hazard Statement(s): Harmful if swallowed Pictogram(s) or Symbol(s): Precautionary Statement(s): [Prevention] Do not eat, drink or smoke when using this product. Wash hands and face thoroughly after handling. [Response] If swallowed: Call a poison center or doctor if you feel unwell. Rinse mouth. [Disposal] Dispose of contents and container in accordance with local, regional, national regulations (e.g. US: 40 CFR Part 261, EU:91/156/EEC, JP: Waste Disposal and Cleaning Act, etc.). Hazards not otherwise classified: None. [HNOC] 3. COMPOSITION/INFORMATION ON INGREDIENTS Substance/mixture: Substance Components: Apronal Percent: >98.0%(HPLC)(N) CAS RN: 528-92-7 Molecular Weight: 184.24 Chemical Formula: C9H16N2O2 Synonyms: (2-Isopropyl-4-pentenoyl)urea , Allylisopropylacetylcarbamide , Allylisoprorylacetylurea , Apronalide , N-Carbamoyl-2-isopropyl-4-pentenamide Apronal TCI AMERICA Page 2 of 5 4.