ADAP Quarterly NDC Special Review

Total Page:16

File Type:pdf, Size:1020Kb

ADAP Quarterly NDC Special Review ADAP Formulary Report Current List Of Specified Drug Classes and Drugs Effective Between 04/01/2017 and 06/30/2017 DRUG CLASS DRUG NAME PRODUCT DESCRIPTION EFF DATE TERM DATE PA RQRD BRAND *ANDROGENS-ANABOLIC* Nandrolone Decanoate ANABOLIN LA INJ 100MG/ML 06/11/2010 12/31/2029 NO NO ANDROLONE-D INJ 100MG/ML 06/11/2010 12/31/2029 NO NO ANDROLONE-D INJ 200MG/ML 06/11/2010 12/31/2029 NO NO DECA-DURABOL INJ 100MG/ML 06/11/2010 12/31/2029 NO YES DECA-DURABOL INJ 200MG/ML 06/11/2010 12/31/2029 NO YES DECA-DURABOL INJ 50MG/ML 06/11/2010 12/31/2029 NO YES HYBOLIN DECA INJ 100MG/ML 06/11/2010 12/31/2029 NO NO HYBOLIN DECA INJ 50MG/ML 06/11/2010 12/31/2029 NO NO KABOLIN INJ 50MG/ML 06/11/2010 12/31/2029 NO NO NANDROL DEC INJ 100MG/ML 06/11/2010 12/31/2029 NO NO NANDROL DEC INJ 200MG/ML 06/11/2010 12/31/2029 NO NO NANDROL DEC INJ 50MG/ML 06/11/2010 12/31/2029 NO NO NANDROLATE INJ 100MG/ML 06/11/2010 12/31/2029 NO NO NANDROLATE INJ 50MG/ML 06/11/2010 12/31/2029 NO NO NEO-DURABOL INJ 200MG/ML 06/11/2010 12/31/2029 NO NO NEO-DURABOL INJ 50MG/ML 06/11/2010 12/31/2029 NO NO NEO-DURABOLI INJ 100MG/ML 06/11/2010 12/31/2029 NO NO Nandrolone Phenpropionate ANABOLIN INJ 50MG/ML 06/11/2010 12/31/2029 NO NO ANDROLONE INJ 25MG/ML 06/11/2010 12/31/2029 NO NO ANDROLONE 50 INJ 50MG/ML 06/11/2010 12/31/2029 NO NO DURABOLIN INJ 25MG/ML 06/11/2010 12/31/2029 NO YES DURABOLIN INJ 50MG/ML 06/11/2010 12/31/2029 NO YES HYBOLIN INJ 50MG/ML 06/11/2010 12/31/2029 NO NO HYBOLIN IMPR INJ 25MG/ML 06/11/2010 12/31/2029 NO NO HYBOLIN IMPR INJ 50MG/ML 06/11/2010 12/31/2029 NO YES NANDROBOLIC INJ 25MG/ML 06/11/2010 12/31/2029 NO NO NANDROL PHEN INJ 25MG/ML 06/11/2010 12/31/2029 NO NO NANDROL PHEN INJ 50MG/ML 06/11/2010 12/31/2029 NO NO Testosterone ANDRO 100 INJ 100MG/ML 06/11/2010 12/31/2029 NO NO ANDRODERM DIS 2.5MG/24 06/11/2010 12/31/2029 NO YES ANDRODERM DIS 4MG/24HR 06/11/2010 12/31/2029 NO YES ANDRODERM DIS 5MG/24HR 06/11/2010 12/31/2029 NO YES ANDROGEL GEL 1%(25MG) 06/11/2010 12/31/2029 NO YES ANDROGEL GEL 1%(50MG) 01/01/2012 12/31/2029 NO YES ANDROGEL GEL 1.62% 09/30/2011 12/31/2029 NO YES ANDROLAN INJ 100MG/ML 06/11/2010 12/31/2029 NO NO ANDROLAN INJ 25MG/ML 06/11/2010 12/31/2029 NO NO ANDROLAN INJ 50MG/ML 06/11/2010 12/31/2029 NO NO DURA TESTOST INJ 200/ML 06/11/2010 12/31/2029 NO YES HISTERONE INJ 100MG/ML 06/11/2010 12/31/2029 NO NO HISTERONE INJ 50MG/ML 06/11/2010 12/31/2029 NO NO SHOTEST 100 INJ 100MG/ML 06/11/2010 12/31/2029 NO NO SHOTEST 50 INJ 50MG/ML 06/11/2010 12/31/2029 NO NO STRIANT MIS 30MG 06/11/2010 12/31/2029 NO YES TESAMORE 100 INJ 100MG/ML 06/11/2010 12/31/2029 NO NO TESONE 100 INJ 100MG/ML 06/11/2010 12/31/2029 NO NO TESTIM GEL 1%(50MG) 01/01/2012 12/31/2029 NO YES TESTODERM DIS 4MG/24HR 06/11/2010 12/31/2029 NO YES TESTODERM DIS 6MG/24HR 06/11/2010 12/31/2029 NO YES TESTODERM DIS TTS 06/11/2010 12/31/2029 NO YES TESTOJECT-50 INJ 50MG/ML 06/11/2010 12/31/2029 NO NO RT18100 Saturday, July 8, 2017 Page 1 of 279 Confidentiality Notice: This report is for the sole use of the intended recipient(s) and may contain confidential and privileged information. Any unauthorized review, use, disclosure or distribution is strictly prohibited. ADAP Formulary Report Current List Of Specified Drug Classes and Drugs Effective Between 04/01/2017 and 06/30/2017 DRUG CLASS DRUG NAME PRODUCT DESCRIPTION EFF DATE TERM DATE PA RQRD BRAND *ANDROGENS-ANABOLIC* Testosterone TESTOLIN INJ 100MG/ML 06/11/2010 12/31/2029 NO NO TESTONE POW 06/11/2010 12/31/2029 NO NO TESTONE/AQ INJ 100MG/ML 06/11/2010 12/31/2029 NO NO TESTONE/AQ INJ 50MG/ML 06/11/2010 12/31/2029 NO NO TESTOPEL MIS PELLETS 06/11/2010 12/31/2029 NO YES TESTOSTERONE GEL 1%(50MG) 01/01/2012 12/31/2029 NO YES TESTOSTERONE INJ 100MG/ML 06/11/2010 12/31/2029 NO NO TESTOSTERONE INJ 25MG/ML 06/11/2010 12/31/2029 NO NO TESTOSTERONE INJ 50MG/ML 06/11/2010 12/31/2029 NO NO TESTOSTERONE POW 06/11/2010 12/31/2029 NO YES TESTOSTERONE POW MICRONIZ 06/11/2010 12/31/2029 NO YES TESTRO INJ 100MG/ML 06/11/2010 12/31/2029 NO NO TESTRO INJ 50MG/ML 06/11/2010 12/31/2029 NO NO VOGELXO GEL 1%(50MG) 01/01/2012 12/31/2029 NO YES Testosterone Cypionate ANDRO-CYP200 INJ 200MG/ML 06/11/2010 12/31/2029 NO NO DEPANDRO 200 INJ 200MG/ML 06/11/2010 12/31/2029 NO NO DEPOTEST INJ 200MG/ML 06/11/2010 12/31/2029 NO NO DEPO-TESTOST INJ 200MG/ML 06/11/2010 12/31/2029 NO YES D-TES 200 INJ 200MG/ML 06/11/2010 12/31/2029 NO NO DURATEST INJ 200MG/ML 06/11/2010 12/31/2029 NO NO LA TEST 200 INJ 200MG/ML 06/11/2010 12/31/2029 NO NO RU-ANDROSPAN INJ 200MG/ML 06/11/2010 12/31/2029 NO NO TESTOJECT LA INJ 200MG/ML 06/11/2010 12/31/2029 NO NO TESTONE/CYP INJ 200MG/ML 06/11/2010 12/31/2029 NO YES TESTOST CYP INJ 200MG/ML 06/11/2010 12/31/2029 NO NO TESTRED INJ 200MG/ML 06/11/2010 12/31/2029 NO NO VIRILON INJ 200MG/ML 06/11/2010 12/31/2029 NO NO *ANORECTAL AGENTS* Benzocaine (Rectal) AMERICAINE OIN 20% 07/01/2007 12/31/2029 NO YES ANOCAINE SUP 07/01/2007 12/31/2029 NO YES BISCOLAN SUP 07/01/2007 12/31/2029 NO NO HEMET HEMORR SUP 07/01/2007 12/31/2029 NO NO MEDICONE OIN 07/01/2007 12/31/2029 NO NO MEDICONE SUP 07/01/2007 12/31/2029 NO NO MEDICONE SUP 130MG 07/01/2007 12/31/2029 NO YES MEDICONE REC OIN 07/01/2007 12/31/2029 NO YES MEDICONE REC SUP 07/01/2007 12/31/2029 NO YES Benzocaine-Benzethonium (Rectal) AMERICAINE OIN 20% 07/01/2007 12/31/2029 NO YES Benzocaine-Ephedrine HEMOCAINE OIN 07/01/2007 12/31/2029 NO YES PAZO OIN 07/01/2007 12/31/2029 NO YES PAZO SUP 07/01/2007 12/31/2029 NO YES Benzocaine-Phenylephrine RECTAGENE SUP 07/01/2007 12/31/2029 NO YES Benz-Pyril-Phenyleph-Bismuth Subgallate-Zinc Oxide RECTAGENE OIN 07/01/2007 12/31/2029 NO NO Budesonide (Intrarectal) UCERIS AER 2MG/ACT 07/01/2007 12/31/2029 NO YES Calamine-Zinc Oxide (Rectal) VERSAL SUP HEMORRHO 07/01/2007 12/31/2029 NO YES Camphor-Phenol-Tannic Acid-Zinc Oxide (Rectal) MEDICONE OIN MAX ST 07/01/2007 12/31/2029 NO YES PETERSONS OIN HEMORRH 07/01/2007 12/31/2029 NO YES Cocoa Butter-Shark Liver Oil HCA HEMORRHO SUP 79-3% 07/01/2007 12/31/2029 NO NO HEMOR AID SUP 07/01/2007 12/31/2029 NO NO HEMORRHOID SUP PREP 07/01/2007 12/31/2029 NO NO HEMORRHOIDAL SUP 07/01/2007 12/31/2029 NO YES HEMORRHOIDAL SUP H 07/01/2007 12/31/2029 NO NO RT18100 Saturday, July 8, 2017 Page 2 of 279 Confidentiality Notice: This report is for the sole use of the intended recipient(s) and may contain confidential and privileged information. Any unauthorized review, use, disclosure or distribution is strictly prohibited. ADAP Formulary Report Current List Of Specified Drug Classes and Drugs Effective Between 04/01/2017 and 06/30/2017 DRUG CLASS DRUG NAME PRODUCT DESCRIPTION EFF DATE TERM DATE PA RQRD BRAND *ANORECTAL AGENTS* Cocoa Butter-Shark Liver Oil HEMORRHOIDAL SUP PREP 07/01/2007 12/31/2029 NO NO HEMORROID SUP 3% 07/01/2007 12/31/2029 NO YES OSCO HEMORRH SUP 3% 07/01/2007 12/31/2029 NO NO PREPARATION SUP H 07/01/2007 12/31/2029 NO YES PROMPT RELIE SUP 07/01/2007 12/31/2029 NO NO SAV-ON HEMOR SUP 07/01/2007 12/31/2029 NO NO WYANOIDS REL SUP FACTOR 07/01/2007 12/31/2029 NO YES Dibucaine (Rectal) DIBUCAINE OIN 1% 07/01/2007 12/31/2029 NO NO HEMMORHOIDAL OIN & TOP 1% 07/01/2007 12/31/2029 NO NO NUPERCAINAL OIN 1% 07/01/2007 12/31/2029 NO YES RECTACAINE OIN 1% 07/01/2007 12/31/2029 NO NO Diperodon HCl (Rectal) HEMORRHOID OIN 07/01/2007 12/31/2029 NO NO RECTOLATUM OIN 07/01/2007 12/31/2029 NO NO Diperodon-Pyrilamine-Phenylephrine EMEROID CRE 07/01/2007 12/31/2029 NO YES HEMET HEMORR OIN 07/01/2007 12/31/2029 NO NO RECTAL OIN 07/01/2007 12/31/2029 NO YES Ephedrine & Belladonna WYANOID SUP 07/01/2007 12/31/2029 NO YES Hamamelis Water-Glycerin TUCKS CLEAR GEL 07/01/2007 12/31/2029 NO YES Hydrocortisone (Intrarectal) COLOCORT ENE 100MG 07/01/2007 12/31/2029 NO NO CORTENEMA ENE 100MG 07/01/2007 12/31/2029 NO YES HYDROCORT ENE 100MG 07/01/2007 12/31/2029 NO NO Hydrocortisone (Rectal) ANUSOL-HC CRE 2.5% 07/01/2007 12/31/2029 NO YES HEMORRHOIDAL CRE HC 2.5% 07/01/2007 12/31/2029 NO NO HEMORRHOIDAL CRE -HC 2.5% 07/01/2007 12/31/2029 NO NO HYDROCORT CRE 1% 07/01/2007 12/31/2029 NO NO HYDROCORT CRE 2.5% 07/01/2007 12/31/2029 NO NO HYDROCORTISO CRE 2.5% 07/01/2007 12/31/2029 NO NO PROCTOCARE CRE -HC 2.5% 07/01/2007 12/31/2029 NO NO PROCTOCORT CRE 1% 07/01/2007 12/31/2029 NO YES PROCTOCREAM CRE HC 2.5% 07/01/2007 12/31/2029 NO NO PROCTOCREAM CRE -HC 2.5% 07/01/2007 12/31/2029 NO NO PROCTO-KIT CRE 2.5% 07/01/2007 12/31/2029 NO NO PROCTO-MED CRE HC 2.5% 07/01/2007 12/31/2029 NO NO PROCTO-PAK CRE 1% 07/01/2007 12/31/2029 NO NO PROCTOSOL HC CRE 2.5% 07/01/2007 12/31/2029 NO NO PROCTOZONE CRE -HC 2.5% 07/01/2007 12/31/2029 NO NO Hydrocortisone Ace-Pramoxine-Dietary Manage Prod-Cleans Wipe ANALPRAM KIT ADVANCED 07/01/2007 12/31/2029 NO YES Hydrocortisone Acetate (Intrarectal) CORTIFOAM AER 90MG 07/01/2007 12/31/2029 NO YES Hydrocortisone Acetate (Rectal) ANUCORT-HC SUP 10MG 07/01/2007 12/31/2029 NO NO ANUCORT-HC SUP 25MG 07/01/2007 12/31/2029 NO NO ANUGARD-HC SUP 07/01/2007 12/31/2029 NO NO ANU-MED HC SUP 25MG 07/01/2007 12/31/2029 NO NO ANUMED-HC SUP 25MG 07/01/2007 12/31/2029 NO NO ANU-MED-HC SUP 10MG 07/01/2007 12/31/2029 NO NO ANUPREP-HC SUP 10MG 07/01/2007 12/31/2029 NO NO ANUPREP-HC SUP 25MG 07/01/2007 12/31/2029 NO NO ANURX-HC SUP 25MG 07/01/2007 12/31/2029 NO NO ANUSOL-HC CRE 0.5% 07/01/2007 12/31/2029 NO YES ANUSOL-HC CRE 1% 07/01/2007 12/31/2029 NO YES ANUSOL-HC SUP 10MG 07/01/2007 12/31/2029 NO YES ANUSOL-HC SUP 25MG 07/01/2007 12/31/2029 NO NO RT18100 Saturday, July 8, 2017 Page 3 of 279 Confidentiality Notice: This report is for the sole use of the intended recipient(s) and may contain confidential and privileged information.
Recommended publications
  • (12) Patent Application Publication (10) Pub. No.: US 2014/0100249 A1 Sears Et Al
    US 201401.00249A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2014/0100249 A1 Sears et al. (43) Pub. Date: Apr. 10, 2014 (54) THERAPEUTIC TREATMENT A63/37 (2006.01) A613 L/45 (2006.01) (71) Applicants: Douglas Sears, Oak Park, CA (US); A613 L/4458 (2006.01) Michael Reilly, Oak Park, CA (US) (52) U.S. Cl. CPC ............... A61K 45/06 (2013.01); A61 K3I/451 (72) Inventors: Douglas Sears, Oak Park, CA (US); (2013.01): A613 L/4458 (2013.01); A61 K Michael Reilly, Oak Park, CA (US) 3 1/137 (2013.01); A61 K31/165 (2013.01) USPC .......................................................... S14/325 (21) Appl. No.: 14/046,528 (57) ABSTRACT (22) Filed: Oct. 4, 2013 This invention discloses a treatment for a patient receiving O O medication to treat an attention deficit disorder Such as Related U.S. Application Data ADHD wherein the treatment results in a loss of appetite and (60) Provisional application No. 61/744,948, filed on Oct. impairment of the patient's attentiveness. The treatment com 9, 2012, now abandoned. bines a treatment for an attention deficit disorder with an appetite stimulant, wherein the appetite stimulant increases Publication Classification the caloric intake of a patient, which can increase the patients attentiveness. The combination treatment can be given for an (51) Int. Cl. indefinite, including, without limitation, life-long, to allow a A6 IK 45/06 (2006.01) patient to maintain normal caloric intake during treatment for A6 IK3I/65 (2006.01) an attention deficit disorder. 8aasaias: Patent Application Publication Apr. 10, 2014 Sheet 1 of 22 US 2014/010O249 A1 Figure i: improvement in Atiention with increased Caiotic intake 8aakast Patent Application Publication Apr.
    [Show full text]
  • A2) United States Patent (10) Patent No.: US 8,940,711 B2 Olsonet Al
    US008940711B2 a2) United States Patent (10) Patent No.: US 8,940,711 B2 Olsonet al. (45) Date of Patent: Jan. 27, 2015 (54) MICRO-RNA FAMILY THAT MODULATES C1I2N 2310/321 (2013.01); C12N 2310/346 FIBROSIS AND USES THEREOF (2013.01); CI2N 2310/3515 (2013.01); C12N (71) Applicant: The Board of Regents, The University 2320/31 (2013.01); CI2N 2330/10 (2013.01) of Texas System, Austin, TX (US) USPC iececcsesseeseeesenensceesensessecsenesenscnseeee 514/444 (58) Field of Classification Search (72) Inventors: Erie N. Olson, Dallas, TX (US); Eva USPC iececcsesseeseeesenensceesensessecsenesenscnseeee 514/44A van Rooij, Utrecht (NL) See application file for complete search history. (56) References Cited (73) Assignee: The Board of Regents, The University of Texas System, Austin, TX (US) U.S. PATENT DOCUMENTS Notice: Subject to any disclaimer, the term of this 7,232,806 B2 6/2007 Tuschletal. (*) 7,674,617 B2 3/2010 Kim etal. patent is extended or adjusted under 35 2005/0059005 Al 3/2005 Tuschletal. U.S.C. 154(b) by 1 day. 2005/0222399 Al 10/2005 Bentwich 2005/0261218 Al 11/2005 Esau etal. (21) Appl. No.: 13/840,242 2006/0019286 Al 1/2006 Horvitz et al. 2006/0105360 Al 5/2006 Croceet al. Filed: Mar.15, 2013 2006/0185027 Al 8/2006 Bartel etal. (22) 2006/0247193 Al 11/2006 Taira etal. 2007/0087335 Al 4/2007 Brahmacharietal. (65) Prior Publication Data 2007/0092882 Al 4/2007 Wangetal. US 2013/0261169 Al Oct. 3, 2013 2008/0050722 Al 2/2008 Kim etal. 2008/0176766 Al 7/2008 Brown etal.
    [Show full text]
  • Metabolic-Hydroxy and Carboxy Functionalization of Alkyl Moieties in Drug Molecules: Prediction of Structure Influence and Pharmacologic Activity
    molecules Review Metabolic-Hydroxy and Carboxy Functionalization of Alkyl Moieties in Drug Molecules: Prediction of Structure Influence and Pharmacologic Activity Babiker M. El-Haj 1,* and Samrein B.M. Ahmed 2 1 Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, University of Science and Technology of Fujairah, Fufairah 00971, UAE 2 College of Medicine, Sharjah Institute for Medical Research, University of Sharjah, Sharjah 00971, UAE; [email protected] * Correspondence: [email protected] Received: 6 February 2020; Accepted: 7 April 2020; Published: 22 April 2020 Abstract: Alkyl moieties—open chain or cyclic, linear, or branched—are common in drug molecules. The hydrophobicity of alkyl moieties in drug molecules is modified by metabolic hydroxy functionalization via free-radical intermediates to give primary, secondary, or tertiary alcohols depending on the class of the substrate carbon. The hydroxymethyl groups resulting from the functionalization of methyl groups are mostly oxidized further to carboxyl groups to give carboxy metabolites. As observed from the surveyed cases in this review, hydroxy functionalization leads to loss, attenuation, or retention of pharmacologic activity with respect to the parent drug. On the other hand, carboxy functionalization leads to a loss of activity with the exception of only a few cases in which activity is retained. The exceptions are those groups in which the carboxy functionalization occurs at a position distant from a well-defined primary pharmacophore. Some hydroxy metabolites, which are equiactive with their parent drugs, have been developed into ester prodrugs while carboxy metabolites, which are equiactive to their parent drugs, have been developed into drugs as per se.
    [Show full text]
  • (12) United States Patent (10) Patent N0.: US 8,343,962 B2 Kisak Et Al
    US008343962B2 (12) United States Patent (10) Patent N0.: US 8,343,962 B2 Kisak et al. (45) Date of Patent: *Jan. 1, 2013 (54) TOPICAL FORMULATION (58) Field of Classi?cation Search ............. .. 514/226.5, 514/334, 420, 557, 567 (75) Inventors: Edward T. Kisak, San Diego, CA (US); See application ?le fOr Complete Search history. John M. NeWsam, La Jolla, CA (US); _ Dominic King-Smith, San Diego, CA (56) References C‘ted (US); Pankaj Karande, Troy, NY (US); Samir Mitragotri, Goleta, CA (US) US' PATENT DOCUMENTS 5,602,183 A 2/1997 Martin et al. (73) Assignee: NuvoResearchOntano (CA) Inc., Mississagua, 6,328,979 2B1 12/2001 Yamashita et a1. 7,001,592 B1 2/2006 Traynor et a1. ( * ) Notice: Subject to any disclaimer, the term of this 7,795,309 B2 9/2010 Kisak eta1~ patent is extended or adjusted under 35 2002/0064524 A1 5/2002 Cevc U.S.C. 154(b) by 212 days. FOREIGN PATENT DOCUMENTS This patent is subject to a terminal dis- W0 WO 2005/009510 2/2005 claimer- OTHER PUBLICATIONS (21) APPI' NO‘, 12/848,792 International Search Report issued on Aug. 8, 2008 in application No. PCT/lB2007/0l983 (corresponding to US 7,795,309). _ Notice ofAlloWance issued on Apr. 29, 2010 by the Examiner in US. (22) Med Aug- 2’ 2010 Appl. No. 12/281,561 (US 7,795,309). _ _ _ Of?ce Action issued on Dec. 30, 2009 by the Examiner in US. Appl. (65) Prior Publication Data No, 12/281,561 (Us 7,795,309), Us 2011/0028460 A1 Feb‘ 3’ 2011 Primary Examiner * Raymond Henley, 111 Related U 5 Application Data (74) Attorney, Agent, or Firm * Foley & Lardner LLP (63) Continuation-in-part of application No.
    [Show full text]
  • Optum Essential Health Benefits Enhanced Formulary PDL January
    PENICILLINS ketorolac tromethamineQL GENERIC mefenamic acid amoxicillin/clavulanate potassium nabumetone amoxicillin/clavulanate potassium ER naproxen January 2016 ampicillin naproxen sodium ampicillin sodium naproxen sodium CR ESSENTIAL HEALTH BENEFITS ampicillin-sulbactam naproxen sodium ER ENHANCED PREFERRED DRUG LIST nafcillin sodium naproxen DR The Optum Preferred Drug List is a guide identifying oxacillin sodium oxaprozin preferred brand-name medicines within select penicillin G potassium piroxicam therapeutic categories. The Preferred Drug List may piperacillin sodium/ tazobactam sulindac not include all drugs covered by your prescription sodium tolmetin sodium drug benefit. Generic medicines are available within many of the therapeutic categories listed, in addition piperacillin sodium/tazobactam Fenoprofen Calcium sodium to categories not listed, and should be considered Meclofenamate Sodium piperacillin/tazobactam as the first line of prescribing. Tolmetin Sodium Amoxicillin/Clavulanate Potassium LOW COST GENERIC PREFERRED For benefit coverage or restrictions please check indomethacin your benefit plan document(s). This listing is revised Augmentin meloxicam periodically as new drugs and new prescribing LOW COST GENERIC naproxen kit information becomes available. It is recommended amoxicillin that you bring this list of medications when you or a dicloxacillin sodium CARDIOVASCULAR covered family member sees a physician or other penicillin v potassium ACE-INHIBITORS healthcare provider. GENERIC QUINOLONES captopril ANTI-INFECTIVES
    [Show full text]
  • DESCRIPTION Tolazamide Is an Oral Blood-Glucose-Lowering Drug of the Sulfonylurea Class
    TOLAZAMIDE- tolazamide tablet PD-Rx Pharmaceuticals, Inc. ---------- DESCRIPTION Tolazamide is an oral blood-glucose-lowering drug of the sulfonylurea class. Tolazamide is a white or creamy-white powder very slightly soluble in water and slightly soluble in alcohol. The chemical name is 1-(Hexahydro-1 H-azepin-1-yl)-3-( p-tolylsulfonyl)urea. Tolazamide has the following structural formula: Each tablet for oral administration contains 250 mg or 500 mg of tolazamide, USP and the following inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, magnesium stearate, microcrystalline cellulose, and sodium lauryl sulfate. CLINICAL PHARMACOLOGY Actions Tolazamide appears to lower the blood glucose acutely by stimulating the release of insulin from the pancreas, an effect dependent upon functioning beta cells in the pancreatic islets. The mechanism by which tolazamide lowers blood glucose during long-term administration has not been clearly established. With chronic administration in type II diabetic patients, the blood glucose-lowering effect persists despite a gradual decline in the insulin secretory response to the drug. Extrapancreatic effects may be involved in the mechanism of action of oral sulfonylurea hypoglycemic drugs. Some patients who are initially responsive to oral hypoglycemic drugs, including tolazamide tablets, may become unresponsive or poorly responsive over time. Alternatively, tolazamide tablets may be effective in some patients who have become unresponsive to one or more other sulfonylurea drugs. In addition to its blood glucose-lowering actions, tolazamide produces a mild diuresis by enhancement of renal free water clearance. Pharmacokinetics Tolazamide is rapidly and well absorbed from the gastrointestinal tract. Peak serum concentrations occur at 3 to 4 hours following a single oral dose of the drug.
    [Show full text]
  • The In¯Uence of Medication on Erectile Function
    International Journal of Impotence Research (1997) 9, 17±26 ß 1997 Stockton Press All rights reserved 0955-9930/97 $12.00 The in¯uence of medication on erectile function W Meinhardt1, RF Kropman2, P Vermeij3, AAB Lycklama aÁ Nijeholt4 and J Zwartendijk4 1Department of Urology, Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands; 2Department of Urology, Leyenburg Hospital, Leyweg 275, 2545 CH The Hague, The Netherlands; 3Pharmacy; and 4Department of Urology, Leiden University Hospital, P.O. Box 9600, 2300 RC Leiden, The Netherlands Keywords: impotence; side-effect; antipsychotic; antihypertensive; physiology; erectile function Introduction stopped their antihypertensive treatment over a ®ve year period, because of side-effects on sexual function.5 In the drug registration procedures sexual Several physiological mechanisms are involved in function is not a major issue. This means that erectile function. A negative in¯uence of prescrip- knowledge of the problem is mainly dependent on tion-drugs on these mechanisms will not always case reports and the lists from side effect registries.6±8 come to the attention of the clinician, whereas a Another way of looking at the problem is drug causing priapism will rarely escape the atten- combining available data on mechanisms of action tion. of drugs with the knowledge of the physiological When erectile function is in¯uenced in a negative mechanisms involved in erectile function. The way compensation may occur. For example, age- advantage of this approach is that remedies may related penile sensory disorders may be compen- evolve from it. sated for by extra stimulation.1 Diminished in¯ux of In this paper we will discuss the subject in the blood will lead to a slower onset of the erection, but following order: may be accepted.
    [Show full text]
  • Properties and Units in Clinical Pharmacology and Toxicology
    Pure Appl. Chem., Vol. 72, No. 3, pp. 479–552, 2000. © 2000 IUPAC INTERNATIONAL FEDERATION OF CLINICAL CHEMISTRY AND LABORATORY MEDICINE SCIENTIFIC DIVISION COMMITTEE ON NOMENCLATURE, PROPERTIES, AND UNITS (C-NPU)# and INTERNATIONAL UNION OF PURE AND APPLIED CHEMISTRY CHEMISTRY AND HUMAN HEALTH DIVISION CLINICAL CHEMISTRY SECTION COMMISSION ON NOMENCLATURE, PROPERTIES, AND UNITS (C-NPU)§ PROPERTIES AND UNITS IN THE CLINICAL LABORATORY SCIENCES PART XII. PROPERTIES AND UNITS IN CLINICAL PHARMACOLOGY AND TOXICOLOGY (Technical Report) (IFCC–IUPAC 1999) Prepared for publication by HENRIK OLESEN1, DAVID COWAN2, RAFAEL DE LA TORRE3 , IVAN BRUUNSHUUS1, MORTEN ROHDE1, and DESMOND KENNY4 1Office of Laboratory Informatics, Copenhagen University Hospital (Rigshospitalet), Copenhagen, Denmark; 2Drug Control Centre, London University, King’s College, London, UK; 3IMIM, Dr. Aiguader 80, Barcelona, Spain; 4Dept. of Clinical Biochemistry, Our Lady’s Hospital for Sick Children, Crumlin, Dublin 12, Ireland #§The combined Memberships of the Committee and the Commission (C-NPU) during the preparation of this report (1994–1996) were as follows: Chairman: H. Olesen (Denmark, 1989–1995); D. Kenny (Ireland, 1996); Members: X. Fuentes-Arderiu (Spain, 1991–1997); J. G. Hill (Canada, 1987–1997); D. Kenny (Ireland, 1994–1997); H. Olesen (Denmark, 1985–1995); P. L. Storring (UK, 1989–1995); P. Soares de Araujo (Brazil, 1994–1997); R. Dybkær (Denmark, 1996–1997); C. McDonald (USA, 1996–1997). Please forward comments to: H. Olesen, Office of Laboratory Informatics 76-6-1, Copenhagen University Hospital (Rigshospitalet), 9 Blegdamsvej, DK-2100 Copenhagen, Denmark. E-mail: [email protected] Republication or reproduction of this report or its storage and/or dissemination by electronic means is permitted without the need for formal IUPAC permission on condition that an acknowledgment, with full reference to the source, along with use of the copyright symbol ©, the name IUPAC, and the year of publication, are prominently visible.
    [Show full text]
  • Deliverable 5.A Interim Report on the Study Results APPENDIX 2
    Deliverable 5.a Interim report on the study results APPENDIX 2: Algorithms used to identify study variables for service contract EMA/2011/38/CN ‐ PIOGLITAZONE November 28th 2012 D5.a Interim report on the study results (Appendix 2) for Service Contract EMA/2011/38/CN PIOGLITAZONE Author(s): Vera Ehrenstein (AUH‐AS) APPENDIX 2. ALGORITHMS USED TO IDENTIFY STUDY VARIABLES Algorithms for AU Database DISEASE/CONDITION ICD-8 CODE (1977-1993) ICD-10 CODE (1994-) Diabetes type 2 250.00; 250.06; 250.07; 250.09 E11.0; E11.1; E11.9 Cancer of bladder 188 C67 Haematuria N/A R31 Haematuria, unspecified B18, K70.0–K70.3, K70.9, K71, K73, Mild hepatic impairment 571, 573.01, 573.04 K74, K76.0 Moderate to severe hepatic 070.00, 070.02, 070.04, 070.06, B15.0, B16.0, B16.2, B19.0, K70.4, impairment 070.08, 573.00, 456.00–456.09 K72, K76.6, I85 Acute myocardial infarction 410 I21-I23 Acute coronary syndrome 410, 413 I20-I24 Ischemic heart disease 410-414 I20-I25 427.09, 427.10, 427.11, 427.19, Congestive heart failure I50, I11.0, I13.0,I13.2 428.99, 782.49; Acute renal failure N/A N17 Diabetic coma N/A E10.0, E11.0, E12.0,E13.0, E14.0 Diabetic acidosis N/A E10.1, E11.1, E12.1,E13.1, E14.1 F10.1-F10.9, G31.2, G62.1, G72.1, Alcoholism 291, 303, 577.10, 571.09, 571.10 I42.6, K29.2, K86.0, Z72.1 Obesity 277.99 E65-E66 D5.a Interim report on the study results (Appendix 2) for Service Contract EMA/2011/38/CN PIOGLITAZONE Author(s): Vera Ehrenstein (AUH‐AS) Algorithms for defining acute events in Denmark, ICD-10 code Event ICD-10 code I21.x, I23.x http://apps.who.int/classifications/icd10/browse/2010/en#/I21
    [Show full text]
  • 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]
  • )&F1y3x PHARMACEUTICAL APPENDIX to THE
    )&f1y3X PHARMACEUTICAL APPENDIX TO THE HARMONIZED TARIFF SCHEDULE )&f1y3X PHARMACEUTICAL APPENDIX TO THE TARIFF SCHEDULE 3 Table 1. This table enumerates products described by International Non-proprietary Names (INN) which shall be entered free of duty under general note 13 to the tariff schedule. The Chemical Abstracts Service (CAS) registry numbers also set forth in this table are included to assist in the identification of the products concerned. For purposes of the tariff schedule, any references to a product enumerated in this table includes such product by whatever name known. Product CAS No. Product CAS No. ABAMECTIN 65195-55-3 ACTODIGIN 36983-69-4 ABANOQUIL 90402-40-7 ADAFENOXATE 82168-26-1 ABCIXIMAB 143653-53-6 ADAMEXINE 54785-02-3 ABECARNIL 111841-85-1 ADAPALENE 106685-40-9 ABITESARTAN 137882-98-5 ADAPROLOL 101479-70-3 ABLUKAST 96566-25-5 ADATANSERIN 127266-56-2 ABUNIDAZOLE 91017-58-2 ADEFOVIR 106941-25-7 ACADESINE 2627-69-2 ADELMIDROL 1675-66-7 ACAMPROSATE 77337-76-9 ADEMETIONINE 17176-17-9 ACAPRAZINE 55485-20-6 ADENOSINE PHOSPHATE 61-19-8 ACARBOSE 56180-94-0 ADIBENDAN 100510-33-6 ACEBROCHOL 514-50-1 ADICILLIN 525-94-0 ACEBURIC ACID 26976-72-7 ADIMOLOL 78459-19-5 ACEBUTOLOL 37517-30-9 ADINAZOLAM 37115-32-5 ACECAINIDE 32795-44-1 ADIPHENINE 64-95-9 ACECARBROMAL 77-66-7 ADIPIODONE 606-17-7 ACECLIDINE 827-61-2 ADITEREN 56066-19-4 ACECLOFENAC 89796-99-6 ADITOPRIM 56066-63-8 ACEDAPSONE 77-46-3 ADOSOPINE 88124-26-9 ACEDIASULFONE SODIUM 127-60-6 ADOZELESIN 110314-48-2 ACEDOBEN 556-08-1 ADRAFINIL 63547-13-7 ACEFLURANOL 80595-73-9 ADRENALONE
    [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]