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Order in Council 1243/1995

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PROVINCE OF BRITISH COLUMBIA ORDER OF THE LIEUTENANT GOVERNOR IN COUNCIL Order in Council No. 12 4 3 , Approved and Ordered OCT 121995 Lieutenant Governor Executive Council Chambers, Victoria On the recommendation of the undersigned, the Lieutenant Governor, by and with the advice and consent of the Executive Council, orders that Order in Council 1039 made August 17, 1995, is rescinded. 2. The Drug Schedules made by regulation of the Council of the College of Pharmacists of British Columbia, as set out in the attached resolution dated September 6, 1995, are hereby approved. (----, c" g/J1"----c- 4- Minister of Heal fandand Minister Responsible for Seniors Presidin Member of the Executive Council (This pan is for adnwustratlye purposes only and is not part of the Order) Authority under which Order Is made: Act and section:- Pharmacists, Pharmacy Operations and Drug Scheduling Act, section 59(2)(1), 62 Other (specify): - Uppodukoic1enact N6145; Resolution of the Council of the College of Pharmacists of British Columbia ("the Council"), made by teleconference at Vancouver, British Columbia, the 6th day of September 1995. RESOLVED THAT: In accordance with the authority established in Section 62 of the Pharmacists, Pharmacy Operations and Drug Scheduling Act of British Columbia, S.B.C. Chapter 62, the Council makes the Drug Schedules by regulation as set out in the attached schedule, subject to the approval of the Lieutenant Governor in Council. Certified a true copy Linda J. Lytle, Phr.) Registrar DRUG SCHEDULES to the Pharmacists, Pharmacy Operations and Drug Scheduling Act of British Columbia The Drug Schedules have been printed in an alphabetical format to simplify the process of locating each individual drug entry and determining its status in British Columbia. Each entry is preceded by a code noted as "S-P-D." S = Schedule (A or B) P = Part (1, 2, 3, or 4) D = Division (1, 2, or 3) Drugs listed in Schedule A must be sold from licensed pharmacies. Schedule B drugs may be sold from nonpharmacy outlets. The various Schedules, Parts, and Divisions are further differentiated as follows: A-1 Schedule A, Part 1 (Prescription) Drugs that may be sold by a pharmacist to a practitioner, or on the prescription of a practitioner, anti includes drugs listed in Schedule G of the Food and Drugs Act, Schedule F of the Regulations to the Food and Drugs Act, the Schedule to the Narcotic Control Act, and certain selected additional drugs. A-1-A Schedule A, Part IA (Triplicate Prescription Program) Drugs that may be sold by a pharmacist to a practitioner or on the prescription of a practitioner in accordance with Bylaw B-19(16). A-1-X Schedule A, Part I (Exemptions for Veterinary Purposes) Drugs which may be sold by a pharmacist for veterinary purposes provided that the drugs are stored in an area to which there is no public access, and provided that the drugs are clearly labeled as required by Bylaw 13-19(11) or if the original container is clearly labeled as "For Veterinary Use Only" and a record is kept of: a) Date of sale b) Name, address and signature of purchaser c) Name and quantity of drug sold d) Kind of animal and purpose for which drug is required e) Signature of pharmacist (seller) oteu-15/tmd A-2 Schedule A, Part 2 (Poison Signature) Drugs which may be sold by a pharmacist to any person after the sale is entered in the Poison Register and the drug is labeled as provided in Section 29 of the Pharmacists, Pharmacy Operations and Drug Scheduling Act. A-3-1 Schedule A, Part 3, Division 1 (Poison Label) Drugs that may be sold by a pharmacist to any person but must be labeled "Poison" when repackaged in a pharmacy. A-3-2 Schedule A, Part 3, Division 2 (No Public Access) Drugs that must be stored in an area of the pharmacy to which there is no public access and can be sold by a pharmacist to any person. A-3-3 Schedule A, Part 3, Division 3 (Professional Products Area) Drugs that may be sold by a pharmacist to any person. Entries are "by reference," meaning that any drug not specifically listed elsewhere in the Schedules is considered to be included in this section. B-1 Schedule B, Part 1 Drugs that may be sold by a nonpharmacist to any person. 11-2 Schedule B, Part 2 Drugs that may be sold by a nonpharmacist to any person, provided the drugs are: (1) contained in a product which is registered as a Proprietary Medicine under Division 10 of the Regulations to the Food and Drugs Act, or (2) contained in any other product when the drug's dosage does not exceed that of a product registered in (1) above, and when the product is recommended to treat the same condition as is the Proprietary Medicine and when the package size of the product qualifies for registration as in (1). B-3 Schedule B, Part 3 Drugs that may be sold by a nonpharmacist to any person, provided the drugs are: (1) offered for sale in original packages containing not more than 8 doses, and (2) clearly labeled "For Aquarium Use Only." 15 September 1995 B-4 Schedule B, Part 4 Drugs that may be sold by a nonphannacist to any person, provided the drugs are: (1) sold in the original, labeled container as packaged by the manufacturer, and (2) labeled to identify the concentration of each drug and specific directions for use where the recommended dose does not exceed the amount shown, and (3) not sold after a date on which the drug is indicated or labeled to expire. In general, if any one ingredient of a combination product falls under Part 1, the entire product is considered to be in Part 1. Similarly, if one ingredient of a combination product falls under the no-public-access division of Part 3, the product must not be accessible to the public. The Pharmacists, Pharmacy Operations and Drug Scheduling Act defines "drug" as a substance or combination of substances used, or for use, in or on the body of a person or animal a) to prevent, diagnose, treat or mitigate a disease, disorder or abnormal physical or mental state or a symptom of them, or b) to restore, correct or modify organic functions, and includes a prescribed substance or combination of substances; DRUG SCHEDULES S = Schedule, P = Part, D = Division. Please refer to Page 1 for details of distribution requirements. S-P-D DRUG A-1 ACEBUTOLOL and its salts A-1 ACEPROMAZINE and its salts B-2 ACETAMINOPHEN, maximum 325 mg per dosage unit in package size of 24 dosage units or less A-1 ACETANILDE A-1 ACETAZOLAMIDE A- I ACETOHEXAMIDE B-1 ACETONE A-1 ACETYLCARBROMAL A-1 ACETYLCHOLINE CHLORIDE A-3-2 ACETYLCYSTEINE (see "N-Acetylcysteine") B-2 ACETYLSALICYLIC ACID, maximum 325 mg per dosage unit in package size of 50 dosage units or less A-3-2 ACETYLSALICYLIC ACID, when labeled for pediatric use B-1 ACHILLEA 15 September 1995 S-P-D DRUG Page 4 B-I ACID ACETIC B-1 ACID BENZOIC B-2 ACID BORIC B-1 ACID MURIATIC B-1 ACID SULPHURIC (commercial) A-1 ACONIAZIDE and its salts A-2 ACONITE and its alkaloids and their preparations (except external preparations containing less than 0.2% aconitinc) B-3 ACRIFLAVINE A-1 ACTH (see "corticotropin") A-1 ACTINOMYCIN D and its salts and derivatives A-1 ACYCLOVIR and its salts A-1 ADENOSINE and its salts, when sold or recommended for intravenous administration A-3-2 ADONIS VERNALIS A-1 ADRENOCORTICAL HORMONES and their salts and derivatives (except hydrocortisone or hydrocortisone acetate, when sold as single medicinal ingredients in a concentration of 0.5% in preparations for topical use on the skin) A-3-2 AEROSOL BRONCHODILATORS (other than those containing drugs listed in Schedule A, Part 1) B-1 AGAR B-1 AGRIMONY B-1 ALCIOXA B-2 ALCOHOL ANHYDROUS B-2 ALCOHOL ISOPROPYL A 3-2 ALCOHOLIC MEDICINALS as approved by the Liquor Control and Licensing Branch B-1 ALETRIS A-1 ALFACALCIDOL A-2 ALKALOIDS (all alkaloids not specifically listed elsewhere in these schedules) A-1 ALKYL NITRITES (including amyl nitrite and isobutyl nitrite) A-3-2 ALL NEW NONPRESCRIPTION DRUGS B-1 ALLANTOIN A-I ALLOPURINOL A-I ALLYLISOPROPYLACETYLUREA B-2 ALOE B-2 ALOIN A-I ALPHA-CHLORALOSE (see "chloral") A-1 ALPHAXALONE A-1 ALPHODOLONE and its salts A-1 ALPRAZOLAM B-1 ALTHEA A-1 ALTRENOGEST 15 September 1995 S-P-D DRUG Page 5 A-1 ALTRETAMINE B-1 ALUM-AMMONIUM ALUM (see "ammonium aluminum sulfate") B-1 ALUMINUM ACETATE B-1 ALUMINUM CHLORHYDROXIDE B-1 ALUMINUM CHLORHYDROXIDE PROPYLENE GLYCOL COMPLEX B-2 ALUMINUM HYDROXIDE B-1 ALUMINUM SULFATE B-2 ALUMINUM ZIRCONYL HYDROCHLORIDE COMPLEX B-1 ALUM-POTASH ALUM (see "potassium aluminum sulphate") A-I AMANTADINE and its salts A-1 AMBENONIUM CHLORIDE A-1 AMIKACIN and its salts and derivatives A-1 AMILORIDE and its salts B-2 AMINOACRIDINE HCL A-1 AMINOCAPROIC ACID A-1 AMINOGLUTETHIMIDE A-1 AMINOPHYLLINE A-1 4-AMINO-N-METHYLPTEROYL GLUTAMIC ACID and its salts A-1 AMINOPTERIN and its salts A-1 4-AMINO-PTEROYL ASPARTIC ACID and its salts A-1 4-AMINOSALICYLIC ACID and its salts A-1 AMINOPYRINE and its derivatives A-1 5-AMINOSALICYLIC ACID A-1 AMIODARONE and its salts A-1 AMITRAZ A-1 AMITRIPTYLINE and its salts A-1 AMLODIPINE and its salts B-1 AMMONIA B-1 AMMONIACUM A-2 AMMONIATED MERCURY (see "mercurial salts") B-I AMMONIUM ACETATE B-1 AMMONIUM ALUMINUM SULPHATE (alum-ammonium alum) B-1 AMMONIUM BICARBONATE A-1 AMMONIUM BROMIDE B-1 AMMONIUM CARBONATE B-1 AMMONIUM CITRATE (in cough preparations only) B-1 AMMONIUM CHLORIDE (in cough preparations only) B-1 AMMONIUM TARTRATE A-1 AMOXAPINE A-1 AMOXICILLIN and its salts and derivatives A-1 AMPHETAMINE and its salts 15 September 1995 S-P-D DRUG Page 6 A-1 AMPHOTERICIN B and its salts and derivatives A-1 AMPICILLIN and its salts and derivatives A-1
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    1 Part I Biopharmaceuticals Translational Medicine: Molecular Pharmacology and Drug Discovery First Edition. Edited by Robert A. Meyers. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA. Published 2018 by Wiley-VCH Verlag GmbH & Co. KGaA. 3 1 Analogs and Antagonists of Male Sex Hormones Robert W. Brueggemeier The Ohio State University, Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Columbus, Ohio 43210, USA 1Introduction6 2 Historical 6 3 Endogenous Male Sex Hormones 7 3.1 Occurrence and Physiological Roles 7 3.2 Biosynthesis 8 3.3 Absorption and Distribution 12 3.4 Metabolism 13 3.4.1 Reductive Metabolism 14 3.4.2 Oxidative Metabolism 17 3.5 Mechanism of Action 19 4 Synthetic Androgens 24 4.1 Current Drugs on the Market 24 4.2 Therapeutic Uses and Bioassays 25 4.3 Structure–Activity Relationships for Steroidal Androgens 26 4.3.1 Early Modifications 26 4.3.2 Methylated Derivatives 26 4.3.3 Ester Derivatives 27 4.3.4 Halo Derivatives 27 4.3.5 Other Androgen Derivatives 28 4.3.6 Summary of Structure–Activity Relationships of Steroidal Androgens 28 4.4 Nonsteroidal Androgens, Selective Androgen Receptor Modulators (SARMs) 30 4.5 Absorption, Distribution, and Metabolism 31 4.6 Toxicities 32 Translational Medicine: Molecular Pharmacology and Drug Discovery First Edition. Edited by Robert A. Meyers. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA. Published 2018 by Wiley-VCH Verlag GmbH & Co. KGaA. 4 Analogs and Antagonists of Male Sex Hormones 5 Anabolic Agents 32 5.1 Current Drugs on the Market 32 5.2 Therapeutic Uses and Bioassays
  • Title 16. Crimes and Offenses Chapter 13. Controlled Substances Article 1

    Title 16. Crimes and Offenses Chapter 13. Controlled Substances Article 1

    TITLE 16. CRIMES AND OFFENSES CHAPTER 13. CONTROLLED SUBSTANCES ARTICLE 1. GENERAL PROVISIONS § 16-13-1. Drug related objects (a) As used in this Code section, the term: (1) "Controlled substance" shall have the same meaning as defined in Article 2 of this chapter, relating to controlled substances. For the purposes of this Code section, the term "controlled substance" shall include marijuana as defined by paragraph (16) of Code Section 16-13-21. (2) "Dangerous drug" shall have the same meaning as defined in Article 3 of this chapter, relating to dangerous drugs. (3) "Drug related object" means any machine, instrument, tool, equipment, contrivance, or device which an average person would reasonably conclude is intended to be used for one or more of the following purposes: (A) To introduce into the human body any dangerous drug or controlled substance under circumstances in violation of the laws of this state; (B) To enhance the effect on the human body of any dangerous drug or controlled substance under circumstances in violation of the laws of this state; (C) To conceal any quantity of any dangerous drug or controlled substance under circumstances in violation of the laws of this state; or (D) To test the strength, effectiveness, or purity of any dangerous drug or controlled substance under circumstances in violation of the laws of this state. (4) "Knowingly" means having general knowledge that a machine, instrument, tool, item of equipment, contrivance, or device is a drug related object or having reasonable grounds to believe that any such object is or may, to an average person, appear to be a drug related object.