Order in Council 1008/1950

Total Page:16

File Type:pdf, Size:1020Kb

Order in Council 1008/1950 1008. Approved and ordered this 18th day of May , A.D. 1950. At the Executive Council Chamber, Victoria, bieute.iiant-Gov PRESENT: The Honourable in the Chair. Mr. Johnson Mr. Turnbull Mr. Straith Mr. Wismer Mr. MacDonald Mr. Carson Mr. Cates Mr. Mr. Mr. Mr. To His Honour The Lieutenant-Governor in Council: The undersigned has the honour to recommend: THAT under Section 40 of the "Pharmacy Act", being Lhapter 251, "Revised Statutes of British Columbia, 19118" the resolution of the Council of the Pharmaceutical Association of the Province of British Columbia passed on the 7th day of March, 1950, a copy of which is attached hereto, be approved. DATED THIS Li-4K day of A.D., 1950. nister of Health and Welfare. APPROVED THIS day of A.D., 1950. Presiding Member of the Executive Council. )4 (dr (a) /p/6 ,4, e'" ...:-r 11A%(... Je"( //.1/ ass I. &mere, Attars'''.Oenerslos Dopartmont, 31st Nay, 1950. BUILDINOS. res Ordor-in-Oounoil Mo, 100e, 1950, Amendments to I mobilo herewith • eopy of Order-in-Council No. 10041, 1910, approving meendments to liehedulse of the "Phormasy Ast'. You will require to have Imowledge of them emendmento in order that your Stet doe may be up to data. for R. A. hnnington, Deputy Provincial flosrotery. 6IG loo8 ISO AMENDMENTS TO SCHEDULES OF THE PHARMACY ACT OF BRITISH COLUMBIA Under authority of Section 40 of the Pharmacy lot of the Province of British Columbia, the Council of the Pharmaceutical Association of the Province of British Columbia, assembled in open session of the Council, do this day declare that the articles or preparations listed in Schedule A, Part I, of the Pharmacy Lot of the Province of British Columbia be struck out and the following substituted: le AminopyrinS and any salt, homologue or deriva.- r. tive thereof: 2. Amphetamine, and any salt thereof: 3. Apiol: 4, Atropine and salts and preparations thereof: 5. Aureomycin: 6, Barbituric koid, and any salt, homologue or derivative thereof: 7. Bromoform: 8. Butyl Chloral Hydrate: " 9, Chloria Hydrate: 10, Cinohophen and Neooinchophen: 11, Codeine and its salts and their preparations, except preparations containing one-eighth grain or less of codeine per tablet or other solid form, or liquid preparations containing one- third grain or less of codeine per fluid ounce, when such preparations are combined with other medicinal ingredients and the maximum dose prescribed for the preparation contain' (1) one such ingredient not less in quantity than the amount prescribed by the British Pharmacopoeia as a minimum dose for such ingredient; (11) two such ingredients having a similar action, each not lees in quantity than one-half the amount prescribed by the British Pharmacopoeia as a minimum dose for each such ingredient respectively; or (111) three such ingredients having a similar action each not less in quantity than one-third the amount prescribed by the British Pharmacopoeia as a minimum dose for each such ingredient respectively, 12. 1-desoxyephedrine, and any salt thereof: 13. Emetine: 14. Ergot, and alkaloids and preparations thereef: 156 hydrocyanic Acid (Prussio): 16. Hyosoine (Scopolamine), and preparations thereof: 17. hyosoyamys and preparations thereof: 18. Hethedrine, and any salt thereof: 19. Nitro-glyoerin: ia 20. Ortho-dinitrophenol, and any compound, homologue or derivatives thereof: ()/$17e' 21. Paraldehyde: 22. Penicillin, its salts, or derivatives or prepar- ations thereof excluding preparations for oral use that contain not more than 3,000 Internation- al Units per dose: except where sold for veterin- ary purposes in oonformity with requirements of Food and Drugs Aot (Canada). 23. Pervertin, and any salt thereof: 24. Phenytoin Sodium: 25. Streptomyoin and any compound thereof: 26. Strpphanthua and preparations thereof: 27. Sulphonamides, and any salt, homologue •r derivative thereof, except where sold for veter- inary purposes in conformity with requirements of Food and Drags lot (Canada). 28. Tetraethylthiuram disulphide: Thiouraoil and any deritiveva or homologue atej4 -5. 29. thereof: 30. Thyroid: 31. Thyroxin, and any salt thereof: 32.Urethane: 33. Yohimba, alkaloids and preparations thereof: An that the article listed in Schedule A, Part II, as item 26, namely Urethanes, be struck out. An that Schedule A, Part III, be amended by the inclusion of the Antihistaminic group, and that the present Schedule A, Part III, be re-numbered including this Antihista- minic group of drugs in its proper alphabetical order, namely: - 3 - xl. Acetanilid and preparations thereof: x2. Acid. Acetic (thirty-three per oentum or stronger): 3. Acid Ametylsalioylic, whether described as Aspirin, Aoetophen, or any other trade- name, mark or designation: x4. Acid Chromic: x5. Acid Oxalic: x6. Acid Pieria (Trinitrophenol): 7. Acid Salicylic: S. Aloes and preparations thereof: x9. Amyl Nitrite: 10. Antihistaminic agents, or histamine antagonists of the metabolic blocking type used for the relief of allergic symptoms, inoluding ethylenediamine derivatives and other synthetic compounds with analagouA pharmacological action, by whatever names or trade names, or for whatever purpose they may be offered for sale or sold, for example: Alubrine, Antergan, Anthallin, Anthisan, Anthophyllin, Antis tine, Benadryl, Bromobenzyl Bromothen, Chlorothen, Deeapryn, Diatrin Hydrochloride, Hetramine, Histadyl, Hydryllin, Linadryl, Neoantergan, Neo-Antergan Maleate, Neohetramine, Phenergan, Pyribenzamine, Pyrrolazote, Tagathen, Thenyl (D.P.E.), Thenylene Hydrochloride, Thephorin„ Tripolon, Trimeton, 3015 R.P., 3277 R.P., and preparations thereof: 11. Aristol: x12. Arsenic, Belladonna, and Stryohnine, when combined with other ingredients in prepara- tions of pills, capsules, tablets, elixirs, or syrups having medicinal qualities other than those possessed by the drugs named in this clause when taken alone, and in doses not exceeding those of the British Pharma- copoeia and generally recognised as safe medication: x13, Barium Chloride: x14, Barium Sulphide: 15. Benzoli 16. Beta Napthol: 17, Bismuth salts and preparations thereof: x18. Butyn: 19. Caffeine and preparations and compounds thereof: 4 x20. Calabar Beans, the alkaloids and prepara- tions thereof: 21. Calomel: 22. Carbon tetrachloride: 23. Cerium Oxalate: 24. Chloretane: x23. Colchicum and preparations thereof: x26. Corrosive Sublimate (tablets only): x27. Cotton Root and preparations thereof: x88. Creosote: x29. Cresol (Cresylio Aoid) and its preparations and the Homologues of Cresol, and their preparations: x30. Crude Carbolic Acid: x31. Dorris Root: x32. Digitalis and preparations thereof: x33. Ephedrine Salts: x34. Ethyl Chloride: 35. Fluid Extracts, except those included elsewhere in these Sohedulee: x36. Formaldehyde, whether described as Formalin or any other trade-name, mark or designation: 37. Formin, whether described as Urotropin, Urosal, Urosine, or any other trade...name, mark, or designation: x38. Galsemium and preparations thereof: x39. Ouaiemol: x40. Hellebore: x41. Henna: 42. Iohthyol and preparations thereof: 43. Insulin: x44. Iodine and preparations thereof: 45. Ipecac and preparations thereof: x46. Lead in combination with Oleio Acid whether sold as Diachylon or under any other desig- nation: x47. Lead Acetate: x48. Lead Carbonate: x49. Lead Iodide: x50. Lead Oxide: 51. Menthol: 52. Methylene Blue: x53. Oil of Cedar: x54. Oil of Chenopodium: x55. Pennyroyal: 56. Phenacetin: 41t57. Phenssone (antiApyrine): Arm' x58. Phosphorus in a free state: x59. Piorotoxin: 60. Pituitary gland, the active principles of: 61. Podophyllin: x62. Potassium Biohromate: 63. Potassium Bromide: 64. Potassium Chloride: x65• Potassium Hydroxide: 66. Potassium Iodide: x67. Potassium Permanganate: 686 Resoroln: x69. Sabadilla seeds: 70. Salioih: 71. Sala: 72. Salophen: x73. Silver Nitrate: x74. Sodium Fluoride: x75. Sodium Hydroxide: x76. Sodium Nitrite: x77. Stavesacre: x78. 3tramonium and preparations thereof: 79. Strontium salts (compounds and preparations except nitrate): x80. Suiphonal, its derivatives: 81. Suprarenal gland, the active principles of: their salts: x82. Thallium salts: 83. Valerian and preparations thereof: x84. Verdigris: x85* Zino Acetate: x86. Zino Chloride; and x87. Zino Sulphate. Done and passed in open Council at Victoria* B. C., this 7th day of Nhroh, A.D. 1950. SIGNED: ai %,Ve74"5 Registrari Seo;141:fteasurer. .
Recommended publications
  • Specialty Direct Supply Drug List
    DRAFT SPECIALTY DIRECT SUPPLY DRUG LIST (DSDL) 9/27/2005 Drug Description Effective Date 5-HT3 Receptor Antagonists ALOXI - SOLN 12/09/2004 ANZEMET - SOLN 12/09/2004 ANZEMET - TABS 12/09/2004 KYTRIL - SOLN 12/09/2004 KYTRIL - TABS 12/09/2004 Additional Solids ALPROSTADIL - POWD 12/09/2004 PROSTAGLANDIN E1 - POWD 12/09/2004 Agents for Gaucher Disease CEREZYME - SOLR 12/09/2004 Agents for Pheochromocytoma PHENTOLAMINE MESYLATE - SOLR 12/09/2004 REGITINE - SOLR 12/09/2004 Alkylating Agents CARBOPLATIN - SOLN 12/09/2004 CARBOPLATIN - SOLR 12/09/2004 CISPLATIN - SOLN 12/09/2004 CISPLATIN AQ - SOLN 12/09/2004 ELOXATIN - SOLR 12/09/2004 MYLERAN - TABS 12/09/2004 PARAPLATIN - SOLN 12/09/2004 PARAPLATIN - SOLR 12/09/2004 PLATINOL - SOLN 12/09/2004 PLATINOL AQ - SOLN 12/09/2004 THIOPLEX - SOLR 12/09/2004 THIOTEPA - SOLR 12/09/2004 Alpha-Proteinase Inhibitor (Human) ARALAST - SUSR 07/01/2005 PROLASTIN - SUSR 07/01/2005 ZEMAIRA - SOLR 07/01/2005 AMINOGLYCOSIDES APOGEN - SOLN 12/09/2004 GARAMYCIN - SOLN 12/09/2004 GENTAMICIN SULFATE - SOLN 12/09/2004 G-MYCIN - SOLN 12/09/2004 JENAMICIN - SOLN 12/09/2004 NEBCIN - SOLN 12/09/2004 NEBCIN MDV - SOLN 12/09/2004 STORZ-G - SOLN 12/09/2004 TOBI - NEBU 12/09/2004 TOBRAMYCIN SULFATE - SOLN 12/09/2004 TOBRAMYCIN SULFATE FLIPTO - SOLN 12/09/2004 Antianxiety Agents - Misc. rev A Page 1 of 13 MaineCare Direct Supply Drug List (DSDL) Drug Description Effective Date Antianxiety Agents - Misc. - Continued - DROPERIDOL - POWD 12/09/2004 DROPERIDOL - SOLN 12/09/2004 INAPSINE - SOLN 12/09/2004 Antiarrhythmics Type III
    [Show full text]
  • Pharmacy and Poisons (Third and Fourth Schedule Amendment) Order 2017
    Q UO N T FA R U T A F E BERMUDA PHARMACY AND POISONS (THIRD AND FOURTH SCHEDULE AMENDMENT) ORDER 2017 BR 111 / 2017 The Minister responsible for health, in exercise of the power conferred by section 48A(1) of the Pharmacy and Poisons Act 1979, makes the following Order: Citation 1 This Order may be cited as the Pharmacy and Poisons (Third and Fourth Schedule Amendment) Order 2017. Repeals and replaces the Third and Fourth Schedule of the Pharmacy and Poisons Act 1979 2 The Third and Fourth Schedules to the Pharmacy and Poisons Act 1979 are repealed and replaced with— “THIRD SCHEDULE (Sections 25(6); 27(1))) DRUGS OBTAINABLE ONLY ON PRESCRIPTION EXCEPT WHERE SPECIFIED IN THE FOURTH SCHEDULE (PART I AND PART II) Note: The following annotations used in this Schedule have the following meanings: md (maximum dose) i.e. the maximum quantity of the substance contained in the amount of a medicinal product which is recommended to be taken or administered at any one time. 1 PHARMACY AND POISONS (THIRD AND FOURTH SCHEDULE AMENDMENT) ORDER 2017 mdd (maximum daily dose) i.e. the maximum quantity of the substance that is contained in the amount of a medicinal product which is recommended to be taken or administered in any period of 24 hours. mg milligram ms (maximum strength) i.e. either or, if so specified, both of the following: (a) the maximum quantity of the substance by weight or volume that is contained in the dosage unit of a medicinal product; or (b) the maximum percentage of the substance contained in a medicinal product calculated in terms of w/w, w/v, v/w, or v/v, as appropriate.
    [Show full text]
  • WO 2011/156817 Al
    (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date Χ t it o n 1 15 December 2011 (15.12.2011) WO 2011/156817 Al (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C02F1/58 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BR, BW, BY, BZ, (21) International Application Number: CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, PCT/US20 11/040214 DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, 13 June 201 1 (13.06.201 1) KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, (25) Filing Language: English NO, NZ, OM, PE, PG, PH, PL, PT, RO, RS, RU, SC, SD, (26) Publication Language: English SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: 61/354,031 11 June 2010 ( 11.06.2010) (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (71) Applicant (for all designated States except US): MOLY- GM, KE, LR, LS, MW, MZ, NA, SD, SL, SZ, TZ, UG, CORP MINERALS LLC [US/US]; 561 Denver Tech ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, MD, RU, TJ, Center Pkwy, Suite 1000, Greenwood Village, CO 801 11 TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, (US).
    [Show full text]
  • 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
    [Show full text]
  • Changes Highlighted Final Version Date of Issue: 23Rd December 2015
    EPHMRA ANATOMICAL CLASSIFICATION GUIDELINES 2016 Section A Changed Classes/Guidelines: Changes Highlighted Final Version Date of issue: 23rd December 2015 1 A2B ANTIULCERANTS R1997r2 016 Combinations of specific antiulcerants with anti-infectives against Helicobacter pylori are classified according to the anti-ulcerant substance. For example, proton pump inhibitors in combination with these anti-infectives are classified in A2B2. A2B1 H2 antagonists R2002 Includes, for example, cimetidine, famotidine, nizatidine, ranitidine, roxatidine. Combinations of low dose H2 antagonists with antacids are classified with antacids in A2A6. A2B2 Acid Proton pump inhibitors R2003r2 016 Includes esomeprazole, lansoprazole, omeprazole, pantoprazole, rabeprazole. A2B3 Prostaglandin antiulcerants Includes misoprostol, enprostil. A2B4 Bismuth antiulcerants Includes combinations with antacids. A2B9 All other antiulcerants R2002r2 016 Includes all other products specifically stated to be antiulcerants even when containing antispasmodics (see A3). Combinations of low dose H2 antagonists with antacids are classified with antacids in A2A6. Included are, eg carbenoxolone, gefarnate, pirenzepine, proglumide, sucralfate and sofalcone. Herbal combinations are classified in A2C. In Japan, Korea and Taiwan only, sulpiride and other psycholeptics indicated for ulcer use are also included in this group, whilst in all other countries, these compounds are classified in N5A9. Products containing rebamipide for gastric mucosal protection are classified here. Products containing rebamipide and indicated for dry eye are classified in S1K9. A2C OTHER STOMACH DISORDER PREPARATIONS R1994 Includes herbal preparations and also plain alginic acid. Combinations of antacids with alginic acid are in A2A1. 2 A4 ANTIEMETICS AND ANTINAUSEANTS A4A ANTIEMETICS AND ANTINAUSEANTS R1996 Products indicated for vertigo and Meniere's disease are classified in N7C. Gastroprokinetics are classified in A3F.
    [Show full text]
  • Lääkealan Turvallisuus- Ja Kehittämiskeskuksen Päätös
    Lääkealan turvallisuus- ja kehittämiskeskuksen päätös N:o xxxx lääkeluettelosta Annettu Helsingissä xx päivänä maaliskuuta 2016 ————— Lääkealan turvallisuus- ja kehittämiskeskus on 10 päivänä huhtikuuta 1987 annetun lääke- lain (395/1987) 83 §:n nojalla päättänyt vahvistaa seuraavan lääkeluettelon: 1 § Lääkeaineet ovat valmisteessa suolamuodossa Luettelon tarkoitus teknisen käsiteltävyyden vuoksi. Lääkeaine ja sen suolamuoto ovat biologisesti samanarvoisia. Tämä päätös sisältää luettelon Suomessa lääk- Liitteen 1 A aineet ovat lääkeaineanalogeja ja keellisessä käytössä olevista aineista ja rohdoksis- prohormoneja. Kaikki liitteen 1 A aineet rinnaste- ta. Lääkeluettelo laaditaan ottaen huomioon lää- taan aina vaikutuksen perusteella ainoastaan lää- kelain 3 ja 5 §:n säännökset. kemääräyksellä toimitettaviin lääkkeisiin. Lääkkeellä tarkoitetaan valmistetta tai ainetta, jonka tarkoituksena on sisäisesti tai ulkoisesti 2 § käytettynä parantaa, lievittää tai ehkäistä sairautta Lääkkeitä ovat tai sen oireita ihmisessä tai eläimessä. Lääkkeeksi 1) tämän päätöksen liitteessä 1 luetellut aineet, katsotaan myös sisäisesti tai ulkoisesti käytettävä niiden suolat ja esterit; aine tai aineiden yhdistelmä, jota voidaan käyttää 2) rikoslain 44 luvun 16 §:n 1 momentissa tar- ihmisen tai eläimen elintoimintojen palauttami- koitetuista dopingaineista annetussa valtioneuvos- seksi, korjaamiseksi tai muuttamiseksi farmako- ton asetuksessa kulloinkin luetellut dopingaineet; logisen, immunologisen tai metabolisen vaikutuk- ja sen avulla taikka terveydentilan
    [Show full text]
  • Anatomical Classification Guidelines V2021 EPHMRA ANATOMICAL CLASSIFICATION GUIDELINES 2021
    EPHMRA ANATOMICAL CLASSIFICATION GUIDELINES 2021 Anatomical Classification Guidelines V2021 "The Anatomical Classification of Pharmaceutical Products has been developed and maintained by the European Pharmaceutical Marketing Research Association (EphMRA) and is therefore the intellectual property of this Association. EphMRA's Classification Committee prepares the guidelines for this classification system and takes care for new entries, changes and improvements in consultation with the product's manufacturer. The contents of the Anatomical Classification of Pharmaceutical Products remain the copyright to EphMRA. Permission for use need not be sought and no fee is required. We would appreciate, however, the acknowledgement of EphMRA Copyright in publications etc. Users of this classification system should keep in mind that Pharmaceutical markets can be segmented according to numerous criteria." © EphMRA 2021 Anatomical Classification Guidelines V2021 CONTENTS PAGE INTRODUCTION A ALIMENTARY TRACT AND METABOLISM 1 B BLOOD AND BLOOD FORMING ORGANS 28 C CARDIOVASCULAR SYSTEM 36 D DERMATOLOGICALS 51 G GENITO-URINARY SYSTEM AND SEX HORMONES 58 H SYSTEMIC HORMONAL PREPARATIONS (EXCLUDING SEX HORMONES) 68 J GENERAL ANTI-INFECTIVES SYSTEMIC 72 K HOSPITAL SOLUTIONS 88 L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS 96 M MUSCULO-SKELETAL SYSTEM 106 N NERVOUS SYSTEM 111 P PARASITOLOGY 122 R RESPIRATORY SYSTEM 124 S SENSORY ORGANS 136 T DIAGNOSTIC AGENTS 143 V VARIOUS 145 Anatomical Classification Guidelines V2021 INTRODUCTION The Anatomical Classification was initiated in 1971 by EphMRA. It has been developed jointly by Intellus/PBIRG and EphMRA. It is a subjective method of grouping certain pharmaceutical products and does not represent any particular market, as would be the case with any other classification system.
    [Show full text]
  • Buzepide Metiodide/Certolizumab Pegol 1715 Laemia
    Buzepide Metiodide/Certolizumab Pegol 1715 laemia. This may cause or exacerbate hypertension, heart failure, berne; Belg.: Grains de Vals; Vethoine; Braz.: Bilifel†; Boldopeptan†; Chof- oedema, alkalosis, and muscle weakness and damage, and sys- ranina; Composto Emagrecedor†; Emagrevit†; Eparema; Jurubileno†; Pilulas De Witt’s†; Prisoventril†; Solvobil; Ventre Livre†; Canad.: Bicholate; Cho- temic carbenoxolone should therefore be used with caution, if at HO lasyn II; Cholasyn†; Control; Doulax; Extra Strong Formula 12†; Herbal Lax- all, in patients with cardiovascular disease. If hypokalaemia is ative; Herbal Laxative plus Yogurt; Herbal Laxative†; Herbalax†; Herbolax; prolonged, renal impairment can occur. Care is needed in pre- Herborex; Laxaco; Laxative†; Mucinum†; Thunas Laxative†; Chile: Bulgaro- existing hepatic or renal impairment. Regular monitoring of O lax; Fr.: Dragees Fuca; Dragees Vegetales Rex; Grains de Vals; Imegul†; Mu- OH cinum a l’Extrait de Cascara; Hong Kong: Mucinum Cascara†; Ital.: Amaro weight and blood pressure is advised; if hypokalaemia, oedema, Medicinale; Coladren; Combilax; Confetti Lassativi CM; Critichol; Digelax†; or a significant rise in blood pressure occurs, carbenoxolone ther- OO OH Dis-Cinil Complex; Draverex; Eparema; Eparema-Levul; Eupatol; Fave di Fu- apy should be stopped. Potassium depletion may be corrected HO ca; Grani di Vals; Hepatos; Hepatos B12; Lassatina†; Magisbile†; Mepalax; with potassium supplements. Systemic use of carbenoxolone OH Schias-Amaro Medicinale†; Solvobil; Stimolfit; Vadolax†;
    [Show full text]
  • Table 4: Protective Action Criteria (PAC) Rev. 29 Based on Applicable
    Table 4: Protective Action Criteria (PAC) Rev. 29a based on applicable 60-minute AEGLs, ERPGs, or TEELs. The chemicals are 3 listed in alphabetical order and the values are presented in mg/m . June 2018 Table 4 is an alphabetical list of the chemical substances and their corresponding PAC values in mass per unit volume (mg/m3). The conversion of ppm to mg/m3 was carried out assuming normal temperature and pressure, 25°C and 760 mm Hg. The columns presented in Table 4 provide the following information: Heading Definition No. The ordered numbering of the chemicals as they appear in this alphabetical listing Chemical Name The name of the chemical substance submitted to the PAC development team CASRN The Chemical Abstracts Service Registry Number1 for this chemical PAC-1 Based on the applicable AEGL-1, ERPG-1, or TEEL-1 value PAC-2 Based on the applicable AEGL-2, ERPG-2, or TEEL-2 value PAC-3 Based on the applicable AEGL-3, ERPG-3, or TEEL-3 value Chemicals for which AEGLs are available have their chemical name, CASRN, and AEGL values displayed in a bolded and larger font. Chemicals for which ERPGs are available, but not AEGLs, have their chemical name, CASRN, and ERPG values displayed in a bolded font. Chemicals for which TEELs are available, but no AEGLs or ERPGs, have their chemical name, CASRN, and values displayed using a regular font. Additional information on PAC values and TEEL values and links to other sources of information is provided on the Subcommittee on Consequence Assessment and Protective Actions (SCAPA) webpage at http://orise.orau.gov/emi/scapa/default.htm.
    [Show full text]
  • List of Psychoactive Drug Spirits for MD A-Methylfentanyl, Abilify
    List of Psychoactive Drug Spirits for MD A-Methylfentanyl, Abilify, abnormal basal ganglia function, abuse of medicines, Aceperone, Acepromazine, Aceprometazine, Acetildenafil, Aceto phenazine, Acetoxy Dipt, Acetyl morphone, Acetyl propionyl morphine, Acetyl psilocin, Activation syndrome, acute anxiety, acute hypertension, acute panic attacks, Adderall, Addictions to drugs, Addictions to medicines, Addictions to substances, Adrenorphin, Adverse effects of psychoactive drugs, adverse reactions to medicines, aggression, aggressive, aggressiveness, agitated depression, Agitation and restlessness, Aildenafil, Akuammine, alcohol abuse, alcohol addiction, alcohol withdrawl, alcohol-related brain damage, alcohol- related liver damage, alcohol mix with medicines for adverse reaction, Alcoholism, Alfetamine, Alimemazine, Alizapride, Alkyl nitrites, allergic breathing reactions to meds, choking to anaphallectic shock, & death; allergic skin reactions to meds, rash, itchyness, hives, welts, etc, Alletorphine, Almorexant, Alnespirone, Alpha Ethyltryptamine, Alpha Neoendorphin, alterations in brain hormones, alterations in mental status, altered consciousness, altered mind, Altoqualine, Alvimopan, Ambien, Amidephrine, Amidorphin, Amiflamine, Amisulpride, Amphetamines, Amyl nitrite, Anafranil, Analeptic, Anastrozole, Anazocine, Anilopam, Antabuse, anti anxiety meds, anti dopaminergic activity, anti seizure meds, Anti convulsants, Anti depressants, Anti emetics, Anti histamines, anti manic meds, anti parkinsonics, Anti psychotics, Anxiety disorders,
    [Show full text]
  • Formula List with Notes of WH Schieffelin &
    FORMULA LIST WITH NOTES or W. II. Schieffelin & Co.’s SOLUBLE > Pius and Granules, Doses, Tables of Diseases and Remedies, the Metric System, etc. NKW YORK, Dec., 1882. ESTABLISHED 1794. Lawrence &. Schleffelin, 1794. Jacob Schleffelin, 1799. J. Schleffelin & Son, 1803. H. H. Schleffelin & Co., 1813. Schleffelin, Brothers & Co., 1849. W, H. Schleffelin &. Co., 1865. Preface. 3 PREFACE. This little volume is designed as a convenient pocket book of memofanda for the use of physi- cians. It is specially devoted to our Soluble Pills and Granules, and notes concerning them. In pre- senting it we beg to express our obligations to the profession for their favorable opinion of our prep- arations, as evinced not only by the direct expres- sions of leading physicians, but by the equally gratifying demand lor our goods which has recently necessitated the extension of our laboratory facili- ties to double their former capacity. This substan- tial tribute to the uniformly good quality of our goods we shall endeavor to merit in the future as in the past. The materials employed in manufacturing any of our goods are the best that the market affords. It is undoubtedly true that the drug market of the United States has advanced rapidly of late years in the superior quality of imported,as well as domes- tic, crude as well as manufactured goods, and we believe that now our country is at least equally as well supplied in that direction as any other. This satisfactory condition of our market has been brought about by the intelligent efforts of leading American importersand manufacturers, and no one need now experience any difficulty in securing the very best of drugs and chemicals provided he is willing to pay a just price for them.
    [Show full text]
  • Anatomical Classification Guidelines V2018 EPHMRA ANATOMICAL
    EPHMRA ANATOMICAL CLASSIFICATION GUIDELINES 2018 Anatomical Classification Guidelines V2018 "The Anatomical Classification of Pharmaceutical Products has been developed and maintained by the European Pharmaceutical Marketing Research Association (EphMRA) and is therefore the intellectual property of this Association. EphMRA's Classification Committee prepares the guidelines for this classification system and takes care for new entries, changes and improvements in consultation with the product's manufacturer. The contents of the Anatomical Classification of Pharmaceutical Products remain the copyright to EphMRA. Permission for use need not be sought and no fee is required. We would appreciate, however, the acknowledgement of EphMRA Copyright in publications etc. Users of this classification system should keep in mind that Pharmaceutical markets can be segmented according to numerous criteria." EphMRA 2018 Anatomical Classification Guidelines V2018 CONTENTS PAGE INTRODUCTION A ALIMENTARY TRACT AND METABOLISM 1 B BLOOD AND BLOOD FORMING ORGANS 28 C CARDIOVASCULAR SYSTEM 35 D DERMATOLOGICALS 50 G GENITO-URINARY SYSTEM AND SEX HORMONES 59 H SYSTEMIC HORMONAL PREPARATIONS (EXCLUDING SEX HORMONES) 67 J GENERAL ANTI-INFECTIVES SYSTEMIC 71 K HOSPITAL SOLUTIONS 87 M MUSCULO-SKELETAL SYSTEM 104 N NERVOUS SYSTEM 109 P PARASITOLOGY 119 R RESPIRATORY SYSTEM 121 S SENSORY ORGANS 132 T DIAGNOSTIC AGENTS 139 V VARIOUS 142 Anatomical Classification Guidelines V2018 INTRODUCTION The Anatomical Classification was initiated in 1971 by EphMRA. It has been developed jointly by PBIRG and EphMRA. It is a subjective method of grouping certain pharmaceutical products and does not represent any particular market, as would be the case with any other classification system. These notes are known as the Anatomical Classification Guidelines, and are intended to be used in conjunction with the classification.
    [Show full text]