Profile Profile Profile Profile

Total Page:16

File Type:pdf, Size:1020Kb

Profile Profile Profile Profile 127 4. Berl et al. Mechanism of allergic contact dermatitis from Piroxin; Fr. : Brexin; Cycladol; Feldene; Geldene; Inflacedt; 3-(4-[2-(1-p-Chlorobenzoyl-5-methoxy,2-methylindol-3-yia­ V, Proxalyoc; Zofora; Ger.: Brexidolt; Flexaset; Pirobeta; Piroflam; propacetamol: sensitization to activated N,N-diethylglycine. Contad cetoxy)eth)'i}piperazln-1-yl)propyt '4cbenzamldo-N,N,dipro­ 38: Pirox; Gr. : Bleduran; Brexin; Calmopyrol; Conzila; Feldene; Dermatitis I998; 185-8. pylglutaramate dimaieate. 5. Hersch M, et al. Effect of intravenous propacetamol on blood pressure in Fidinor; Flodeneu; Grecotens; Inflamase�N; Neo Axedil; Nilvo; febrile critically patients. Pharmacotherapy 2008; 28: I205-IO. Oximezin; Painrelipt�D; Pedifan; Propanol; Pyrcost; Reumaplus; 076.6 ill C�,HsaCIN50s,2C;H,04� 1 Ruvamed; Sinartrol; Valopon; Zerospasm; Zitumex; Hong Kong: Porphyria. The Drug Database for Acute Porphyria, com­ cinc� s ·-,57,�32�53�3 {,orogh:meracin); 59209-40-4 (.orogturn'eta­ CP-Pirox; Feldene; Mobilist; Piram-Dt; Piroxicat; Sefdene; piled by the Norwegian Porphyria Centre (NAPOS) and Synoxicamt; Vidapirocamt; Hung. : Brexin; Feldene; Flamexin; maleate). the Porphyria Centre Sweden, classifies propacetamol as Hotemin; Pirorheumt; India: Amida; Brexic; Camrox; Camsun; ATC - MOIA814. probably not porphyrinogenic; it may be used as a drug of Cycladol; Dolocare; Dolocip; Dolodil; Dolokam; Dololup; Dolo� ATC vet - 0MO/A8l4. first choice and no precautions are needed.1 nex; Dolopir; Doloswift; Dupox; Estcom; Felcam; Feldex; Flex� UN!/ - F2PUN24B8C ar; Kemonex; Lincitrax; Medicam; Meloxi; Micropec; Mobicam; I. The Drug Database for Acute Porphyria. Available at: http:l/www. drugs-porphyria.org (accessed II !10/11) Mobidin; Movon; Noxicam-MD; Pam; Panorox; Pirox; Suganril; ; Profile Indon.: Faxident; Felcam; Feldene; Infeld; Kifadene; Lanareu­ Proglumetacin maleate, an indoleacetic add derivative P epa at ons ma; Licofel; Maxicamt; Pirocam; Pirodenet; Pirofel; Rexicam; .........r r .......i ................ .......... ......... ....... related to indometacin (p. 71.2), is an NSAID (p. 102.3). It ... Rexil; Rosict; Roxidene; Scandene; Sofdent; Tropidene; Xica� Proprietary Preparations (details are given in Volume B) lorn; Irl.: Feldene; Pericamt; Israel: Brexin; Exipan; Feldene; has been used in musculoskeletal and joint disorders in oral !tal. : Antiflog; Artroxicam; Brexidol; Brexin; Brexivel; Bruxi� doses of up to 600 mg daily, in divided doses. Proglumetacin Single�ingredient Preparations. Gr. : Pro-Dafalgant; Mex. : Tern� camt; Cicladol; Clevian; Dexicamt; Euroxi; Feldene; Flodol; maleate has also been given as rectal suppositories and pra. Ipsoflog; Kinski; Lampoflex; Lenotac; Pirobec; Piroftal; Reuma­ topically as a 5% cream. gil; Roxenet; Roxenilt; Roxiden; Sinartrol; Zelist; Jp n: Baxo; Malaysia: Brexin; Feldene; Rhumagel; Uphaxicam; Mex. : References. l. Appelboom T, Franchimont P. Proglumetacin versus indometacin in Androxicamt; Arlexicam; Artyflam; Asabont; Axtrim; Bapix� rheumatoid arthritis: a double-blind multicenter study. Adv Therapy ied; Bioximil; Brexicam; Brexodin; Brucam; Campirex; Citoken 1994; II: 228-34. T; Dixonal; Dolzycam; Edecamt; Facicam; Feldene; Glandicin; 2. Martens M. Double-blind randomized comparison of proglumetadn and Laspiro; Osteral; Oxi�Reul; Oxicanolt; Pirodaxt; Pirox; Pirox­ naproxen sodium in the treatment of patients with ankle sprains. Curr ant; R�Tyflamt; Reucam; Reutricam; Ripox; Serpicam; Tripirol; Ther Res 1995; 56: 639--48. Vatrem; Neth.: Brexinet; Norw. : Brexidol; NZ: Candyl; Piram- Dt; Pirohexal�Dt; Philipp.: Feldene; Flamastat; Flaxine; Macro� P epa a ons i .....r . r.. ti... .... xam; Neperlant; Palpasin; Parixamt; Pirostadt; Pixacor; Proxi� . ... .. ... ProprietaryPreparations (details are given in Volume B) max; Raxicam; Pol. : Feldene; Flamexin; Hotemint; Port.: Brex­ Propyl nicotinate is used in topical preparations as a in; Feldene; Flexar; Flogocant; Remisil; Reumoxican; Roxazin; Single-ingredient Preparations. Arg.: Bruxel; Belg.: Tolindol; rubefacient. Rus.: Erazon (3pa3oH); Finalgel (<I>rrnarrreni>); S.Afr. : Brexecam; Ger.: Protaxon; Hong Kong: Afloxan; Ital. : Proxil; Jpn: Mirida� Pixicam; Pyrocaps; Rheugesic; Roxifen; Xycam; Singapore: cin; Philipp.: Afloxan; Port. : Protaxil; Thai.: Afloxan. Feldene; Rhumagel; Rosiden; Roxifen; Sefdene; Vitaxicamt; Preparations . ..... .. ..... ....... ....... Spain: Brexinilt; Cycladolt; Feldegel; Feldene; Improntal; Sal­ ProprietaryPreparations (details are given in Volume B) vacam; Sasulen; Vitaxicamt; Swed. : Brexidol; Switz. : Felden; Ger.: Pirocamt; Pirosol; Thai.: Ammidene; Brexin; Butacinon; Cyclo­ Propacetamol Hydrochloride (BANM, r/NNM) Single-ingredient Preparations. Elacur. dex; Dexalin; Fasden; Felcam; Feldene; Felgesic; Felicam; Fel­ Hidrodoruro ropacetamo!; Propac€:tamol, Chiorhydrate nox; Felpac; Felrox; Felxicam; Flamic; Heropedd; Ifemed; de p de; Propacetamof, hidrociOiuro de; Propacetamol-hidroklor• Kobixam; Manoxicam; Maswin; Moxicamt; Neogelt; Neotica; Propyphenazone (BAN, r/NN} id; · Nutarzol; PC�20t; Pherazone; Pi�rock; Pidoxam; Piram; Pirax; . Propacetamolhydroch!orid; Propacetamoi-hydrochforid; lsopropylantipyrine; lsopropylantipyrinum; lsopropylphella­ Piraxil; Pircam; Pirox�Man; Pirox; Piroxal; Piroxam; Piroxcin; Propacetamolhydroklorid; Propacetamoli f1Ydrochlorrdum; · Piroxent; Piroxidon; Piroxone; Piroxsil; Polyxicam; Posedenet; Propacetamolio hldrochloridas; Propasetamolihydrokloridi; zo ne; Propifetiazon; Propifenazoria; Propifenazonas; Propy' Rocki; Roxicam; Roxifen; Roxium; Roxycam; Roxycan; Ruma� nponalieTa Moria V!ApoXJJopt�LI- fenatsoni; Propyfenazoni Propypiienazon; Propyphenazo ne; dene; Rumaxicam; Setarox; Sotilen; Spamic; Verox; Xicam; The hydrochlorider of N/11-diethyiQIYc'ine ester .with Propypnenazonum: flponrir¢er;il30fl Turk.: Cycladol; Felden; Inflamext; Oksikam; UK: Brexidol; cetai11ol; 4-AcetamJdopheriyl diethylaminoacetate hydro­para­ 4-fsopropyi-2,3.Jimethyl-1-phef1}·1-3-pyrazolin-5-one. Feldene; Ukr.: Finalgel (cDimarrreni>); USA: Feldene; Venez. : C:.H,8Nl(}.,230.3 Feldene; Feldenedi; Flamalit; Maxipiro; Pixorid. chloride. Arg.: C45 - 479-91-5. Multi-ingredient Preparations. Buta Rut Bl2; Flexicamin A; Ct,H-,oNz03.HCJ=300.866532-85-2 Flexicamin Bl2; Flexicamin Bl2; Flexicamin; Flogiatrin Bl2; AT(- N028804. CA S -· (p ropacetamoO. Flogiatrin Bl2; Flogiatrin; Peganix; Rumisedan Fuerte; Rumise� AIC Vet--'- -- A TC Ve t N02BE05.- dan; Solocalm Plus; Solocalm Plus; Solocalm�B; Solocalm�Flex; ATC ONO:!BE05 UN/1 nFilRFlt7<;>'Y Braz. : Rheumafim; India: Capsidal; Indon.: Counterpain�PXM; Pharmacopoeias. In Bur. (see p. vii) and Jpn. (}Nil - Sl-t4TQYH8E5. Thai. : Counterpain Plus. Pharmacopoeias. In Bur. (see p. vii). Ph. Eur. 8: (Propyphenazone). A white or slightly yellowish crystalline powder. Slightly soluble in water; freely soluble Ph. Eur. 8: (Propacetamol Hydrochloride). A white or PharmacopoeialPreparafions in alcohol and in dichloromethane. Protect from light. BP 2014: Piroxicam Capsules; Piroxicam Gel; almost white crystalline powder. Freely soluble in water; USP 36: Piroxicam Capsules; Piroxicam Cream. slightly soluble in dehydrated alcohol; practically insoluble in acetone. Protect from moisture. Profile Propyphenazone, a pyrazolone derivative related to Pranoprofen (r!NN) Profile phenazone (p. 124.1), has analgesic and antipyretic properties. It has been given orally and as a rectal Pranoprofe f1<;; ranoprofeno; Pranoprofenum; flpaHonpo­ Propacetamol hydrochloride, a para-aminophenol deriva­ P suppository in the treatment of pain and fever. The usual tive. is hydrolysed to paracetamol (p. 115.1) in the plasma; oral dose is 0.5 to I g up to four times daily. There have been I g of propacetamol hydrochloride is hydrolysed to release ¢eH.a-Meth yt-5H-[1l-benzopyrano[2,3-b]pyridii1,.7-acetic acid. some reports of severe hypersensitivity reactions in patients about 500 mg of paracetamol. It has been given receiving propyphenazone. intramuscularly or intravenously for the treatment of pain C,5H,,-N03S255.3 C4S 5254!/-17-4. and fever. P ep r �r�ti?n.�................ ATC-SOI- BC09. References. Allegaert K, et al. Phannacokinetics of single dose intravenous (details are given in Volume B) ATC Vet QS01 BC09. l. ProprietaryPreparations propacetamol in neonates: effect ot gestational age. Arch Dis Child Fetal UN!! �.2Eil07ET613. 89: Single·ingredient Preparations. Ger.: Demex. Pharmacopoeias. In Jp n. Neonatal Ed 2004; F25-F28. 2. Walson PD, et al. efficacy and tolerability of a single MultHngredient Preparations. Arg.: Algio�Bladuril; Espasmo intravenous dose of acetaminophen prodrug propacetamol in Cibalena; Saridon; Austria: Adolorin; Avamigran; Gewadal; children: a randomized, double-blind, placebo-controlled trial. Clin Ther Melabon; Migradon; Montamed; Nervan; Rapidol; Saridon; Profile 2006; 28: 762-9. Pranoprofen, a propionic acid derivative, is an NSAID 3. Prins SA, et al. Pharmacokinetico;; and analgesic effects of intravenous Spasmoplus; Tonopan; Vivimed; Braz.: Saridon; Tonopan; Chile: Abalgin; Droxelt; Espasmo Cibalgina Compuestat; (p. 102.3). It is used as eye drops in a concentration of 0. 1% propacetamol vs rectal paracetamol in children after major craniofacial surgery. Paediatr Anaesth 2008; 18: 582-92. Espasmo Cibalgina; Gripasan Compuesto DN; Gripasan Com� for ocular inflammation. Pranoprofen has also been given 4. McNicol ED, et a!. Single-dose intravenous paracetamol or propacetamol puesto; SAE; China: Saridon Cz. : Saridon; Valetol; orally for the treatment of pain, inflammation,
Recommended publications
  • Rheumatoid Arthritis (1 of 23)
    Rheumatoid Arthritis (1 of 23) 1 Patient presents w/ signs & symptoms of rheumatoid arthritis (RA) 2 4 DIAGNOSIS No Is RA confi rmed? ALTERNATIVE DIAGNOSIS Yes A Pharmacological therapy • Conventional synthetic disease-modifying anti-rheumatic drug (DMARD) (csDMARD) monotherapy [Methotrexate (preferred), Lefl unomide or Sulfasalazine] • Adjunctive therapy [corticosteroids, nonsteroidal anti-infl ammatory drugs (NSAIDs)] B Non-pharmacological therapy 3 CONTINUE TREATMENT Symptoms improved Yes • at 3 mth & treatment goal Consider decreasing achieved at 6 mth? dose if in sustained remission No A Pharmacological therapy A Add any one of the Pharmacological following: therapy 3 • TNF inhibitor1 or • Change to or add a No Yes • Non-TNF second csDMARD Are poor prognostic factors 1 B present? biological or Non-pharmacological • Jak-inhibitor therapy MIMS B Non- pharmacological therapy TREATMENT © See next page 1In patients who cannot use csDMARDs as comedication, interleukin-6 receptor antagonists & targeted synthetic DMARDs (tsDMARDs) have some advantages over other biological DMARDs (bDMARDs) Not all products are available or approved for above use in all countries. Specifi c prescribing information may be found in the latest MIMS. B105 © MIMS 2020 Rheumatoid Arthritis (2 of 23) TREATMENT OF PATIENTS W/ POOR PROGNOSTIC FACTORS CONT’D CONTINUE 3 TREATMENT RHEUMATOID ARTHRITIS RHEUMATOID Symptoms improved • Yes Consider decreasing at 3 mth & treatment goal dose or increasing achieved at 6 mth? interval if in sustained remission No A Pharmacological therapy • Switch to another TNF inhibitor or non-TNF biological1 or • Jak-inhibitor B Non-pharmacological therapy 3 Symptoms improved Yes at 3 mth & treatment goal achieved at 6 mth? No 1In patients who failed one TNF inhibitor therapy, considerMIMS giving a second TNF inhibitor or changing to an agent from a diff erent class © Not all products are available or approved for above use in all countries.
    [Show full text]
  • S1 Table. List of Medications Analyzed in Present Study Drug
    S1 Table. List of medications analyzed in present study Drug class Drugs Propofol, ketamine, etomidate, Barbiturate (1) (thiopental) Benzodiazepines (28) (midazolam, lorazepam, clonazepam, diazepam, chlordiazepoxide, oxazepam, potassium Sedatives clorazepate, bromazepam, clobazam, alprazolam, pinazepam, (32 drugs) nordazepam, fludiazepam, ethyl loflazepate, etizolam, clotiazepam, tofisopam, flurazepam, flunitrazepam, estazolam, triazolam, lormetazepam, temazepam, brotizolam, quazepam, loprazolam, zopiclone, zolpidem) Fentanyl, alfentanil, sufentanil, remifentanil, morphine, Opioid analgesics hydromorphone, nicomorphine, oxycodone, tramadol, (10 drugs) pethidine Acetaminophen, Non-steroidal anti-inflammatory drugs (36) (celecoxib, polmacoxib, etoricoxib, nimesulide, aceclofenac, acemetacin, amfenac, cinnoxicam, dexibuprofen, diclofenac, emorfazone, Non-opioid analgesics etodolac, fenoprofen, flufenamic acid, flurbiprofen, ibuprofen, (44 drugs) ketoprofen, ketorolac, lornoxicam, loxoprofen, mefenamiate, meloxicam, nabumetone, naproxen, oxaprozin, piroxicam, pranoprofen, proglumetacin, sulindac, talniflumate, tenoxicam, tiaprofenic acid, zaltoprofen, morniflumate, pelubiprofen, indomethacin), Anticonvulsants (7) (gabapentin, pregabalin, lamotrigine, levetiracetam, carbamazepine, valproic acid, lacosamide) Vecuronium, rocuronium bromide, cisatracurium, atracurium, Neuromuscular hexafluronium, pipecuronium bromide, doxacurium chloride, blocking agents fazadinium bromide, mivacurium chloride, (12 drugs) pancuronium, gallamine, succinylcholine
    [Show full text]
  • Protocol Synopsis
    Risk of Upper Gastrointestinal Complications in Users of Nonsteroidal Anti-inflammatory Drugs Study Protocol—V2.0 (Final) October 19, 2009 Prepared by Jordi Castellsague Susana Perez-Gutthann RTI Health Solutions E-mail: [email protected] Federica Pisa, MD, MStat Fabio Barbone, MD, DrPH Udine University, AOUD Udine Institute of Hygiene and Epidemiology E-mail: [email protected] RTI-HS Project No.: 0301655 PROTOCOL APPROVAL SIGNATURE PAGE Project Title : Risk of Upper Gastrointestinal Complications in Users ofNonsteroidal Anti-inflammatory Drugs RTI-HS Project 0301655 Final Appro val Date: October 22,2009 Authors: Jordi Castellsague, MD, MPH; Susana Perez-Gutthann, MD, PhD (RTI­ HS) Fede rica Pisa, MD, MStat; Fabio Barbone, MD, DrPH (Udine University, AOUD Udine) Version: Version 2.0 Final Version Date: October 19, 2009 The following people have reviewed the protocol and give their approval: Susana Perez-Gutthann, MD, PhD Date Global Head Epidemiology RTI Health Solutions / Fabio Barbone, MD, D H Signature Date Director, Institute of Hygiene and Epidemiology University of Udine ii TABLE OF CONTENTS 1 STUDY SYNOPSIS ............................................................................................ 1 2 BACKGROUND ................................................................................................. 4 3 KEY ROLES AND RESPONSIBILITIES ............................................................ 5 3.1.1 Financial Sponsorship ....................................................................................................
    [Show full text]
  • Concomitant Use of Nsaids Or Ssris with Noacs Requires Monitoring for Bleeding
    Original Article Yonsei Med J 2020 Sep;61(9):741-749 https://doi.org/10.3349/ymj.2020.61.9.741 pISSN: 0513-5796 · eISSN: 1976-2437 Concomitant Use of NSAIDs or SSRIs with NOACs Requires Monitoring for Bleeding Min-Taek Lee1, Kwang-Yeol Park2, Myo-Song Kim1, Seung-Hun You1, Ye-Jin Kang1, and Sun-Young Jung1 1College of Pharmacy, Chung-Ang University, Seoul; 2Department of Neurology, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Korea. Purpose: Non-vitamin K antagonist oral anticoagulants (NOACs) are widely used in patients with atrial fibrillation (AF) because of their effectiveness in preventing stroke and their better safety, compared with warfarin. However, there are concerns for an in- creased risk of bleeding associated with concomitant use of non-steroidal anti-inflammatory drugs (NSAIDs) or selective sero- tonin reuptake inhibitors (SSRIs) with NOACs. In this study, we aimed to evaluate the risk of bleeding events in individuals taking concomitant NSAIDs or SSRIs with NOACs after being diagnosed with AF. Materials and Methods: A nested case-control analysis to assess the safety of NSAIDs and SSRIs among NOAC users with AF was performed using data from Korean National Health Insurance Service from January 2012 to December 2017. Among patients who were newly prescribed NOACs, 1233 cases hospitalized for bleeding events were selected, and 24660 controls were determined. Results: The risk of bleeding events was higher in patients receiving concomitant NSAIDs [adjusted odds ratio (aOR) 1.41; 95% confidence interval (CI) 1.24–1.61] or SSRIs (aOR 1.92; 95% CI 1.52–2.42) with NOACs, compared to no use of either drug, respec- tively.
    [Show full text]
  • Prescription Medications, Drugs, Herbs & Chemicals Associated With
    Prescription Medications, Drugs, Herbs & Chemicals Associated with Tinnitus American Tinnitus Association Prescription Medications, Drugs, Herbs & Chemicals Associated with Tinnitus All rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted in any form, or by any means, without the prior written permission of the American Tinnitus Association. ©2013 American Tinnitus Association Prescription Medications, Drugs, Herbs & Chemicals Associated with Tinnitus American Tinnitus Association This document is to be utilized as a conversation tool with your health care provider and is by no means a “complete” listing. Anyone reading this list of ototoxic drugs is strongly advised NOT to discontinue taking any prescribed medication without first contacting the prescribing physician. Just because a drug is listed does not mean that you will automatically get tinnitus, or exacerbate exisiting tinnitus, if you take it. A few will, but many will not. Whether or not you eperience tinnitus after taking one of the listed drugs or herbals, or after being exposed to one of the listed chemicals, depends on many factors ‐ such as your own body chemistry, your sensitivity to drugs, the dose you take, or the length of time you take the drug. It is important to note that there may be drugs NOT listed here that could still cause tinnitus. Although this list is one of the most complete listings of drugs associated with tinnitus, no list of this kind can ever be totally complete – therefore use it as a guide and resource, but do not take it as the final word. The drug brand name is italicized and is followed by the generic drug name in bold.
    [Show full text]
  • Inflammatory Drug
    Abbreviations used: AR(s), adverse hepatotoxicity, 17 reaction(s); ADR(s), adverse drug manufacturers, 9 reaction(s); NSAID(s), non-steroid anti­ amorfazone, trade mark names and inflammatory drug(s) manufacturers, 9 Amuno, generic name and manufacturer, 12 anaemia absorption interactions, drug, 180-1 aplastic, 83 acemetacin, trade mark names and report rate, 33 manufacturers, 8 haemolytic, 84-5 acetyl salicylic acid, see Aspirin in rheumatoid patients, inappropriate action, drug, ~ pharmacoactivity therapy, 250 activation (of drugs), 243-5, 246, 247 anaphylaxis/anaphylactoid reactions, 17, pathway, 244 81 Actol, generic name and manufacturer, 13 Anaprox, generic name and manufacturer, Actosal, generic name and manufacturer, 13 9 angioedema, 6 acyl-coenzyme A formation, 221-2 angiotensin-converting enzyme, 195, 196 adjuvant induced arthritis, ~ inhibitors arthritis function, 195 Af1oxan, generic name and manufacturer, NSAID interactions with, 195-200 14 animal(s) age see also elderly experimentation, ethics of, 267 gastrointestinal susceptibility re­ inter species differences in lated to, 164, 286-8 propionate chiral inversion, use of anti-arthritics correlated 222-3, 223 with, 152 Ansaid, generic name and manufacturer, aged, the, ~ elderly 11 agranulocytosis antacids, 292 incidence, 7, 100-2 passim effect on drug absorption, 180, 181 in Sweden, 66, 67 NSAID interactions with, 185, 193 pyrazolone-induced, 7, 99-104 anthranilic acid, relative safety, 18 analytical epidemiological anti-arthritic drugs, ~ antirheumatic studies, 101-3 drugs
    [Show full text]
  • WO 2013/020527 Al 14 February 2013 (14.02.2013) P O P C T
    (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 WO 2013/020527 Al 14 February 2013 (14.02.2013) P O P C T (51) International Patent Classification: (74) Common Representative: UNIVERSITY OF VETER¬ A61K 9/06 (2006.01) A61K 47/32 (2006.01) INARY AND PHARMACEUTICAL SCIENCES A61K 9/14 (2006.01) A61K 47/38 (2006.01) BRNO FACULTY OF PHARMACY; University of A61K 47/10 (2006.01) A61K 9/00 (2006.01) Veterinary and Pharmaceutical Sciences Brno Faculty Of A61K 47/18 (2006.01) Pharmacy, Palackeho 1/3, CZ-61242 Brno (CZ). (21) International Application Number: (81) Designated States (unless otherwise indicated, for every PCT/CZ20 12/000073 kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (22) Date: International Filing BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, 2 August 2012 (02.08.2012) DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (25) Filing Language: English HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, (26) Publication Language: English ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, (30) Priority Data: NO, NZ, OM, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, 201 1-495 11 August 201 1 ( 11.08.201 1) SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, 2012- 72 1 February 2012 (01.02.2012) TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, 2012-5 11 26 July 2012 (26.07.2012) ZW.
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2005/0249806A1 Proehl Et Al
    US 2005O249806A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2005/0249806A1 Proehl et al. (43) Pub. Date: Nov. 10, 2005 (54) COMBINATION OF PROTON PUMP Related U.S. Application Data INHIBITOR, BUFFERING AGENT, AND NONSTEROIDAL ANTI-NFLAMMATORY (60) Provisional application No. 60/543,636, filed on Feb. DRUG 10, 2004. (75) Inventors: Gerald T. Proehl, San Diego, CA (US); Publication Classification Kay Olmstead, San Diego, CA (US); Warren Hall, Del Mar, CA (US) (51) Int. Cl." ....................... A61K 9/48; A61K 31/4439; A61K 9/20 Correspondence Address: (52) U.S. Cl. ............................................ 424/464; 514/338 WILSON SONS IN GOODRICH & ROSAT (57) ABSTRACT 650 PAGE MILL ROAD Pharmaceutical compositions comprising a proton pump PALO ALTO, CA 94304-1050 (US) inhibitor, one or more buffering agent and a nonsteroidal ASSignee: Santarus, Inc. anti-inflammatory drug are described. Methods are (73) described for treating gastric acid related disorders and Appl. No.: 11/051,260 treating inflammatory disorders, using pharmaceutical com (21) positions comprising a proton pump inhibitor, a buffering (22) Filed: Feb. 4, 2005 agent, and a nonsteroidal anti-inflammatory drug. US 2005/0249806 A1 Nov. 10, 2005 COMBINATION OF PROTON PUMP INHIBITOR, of the Stomach by raising the Stomach pH. See, e.g., U.S. BUFFERING AGENT, AND NONSTEROIDAL Pat. Nos. 5,840,737; 6,489,346; and 6,645,998. ANTI-NFLAMMATORY DRUG 0007 Proton pump inhibitors are typically prescribed for Short-term treatment of active duodenal ulcers, gastrointes CROSS REFERENCE TO RELATED tinal ulcers, gastroesophageal reflux disease (GERD), Severe APPLICATIONS erosive esophagitis, poorly responsive Symptomatic GERD, 0001.
    [Show full text]
  • (CD-P-PH/PHO) Report Classification/Justifica
    COMMITTEE OF EXPERTS ON THE CLASSIFICATION OF MEDICINES AS REGARDS THEIR SUPPLY (CD-P-PH/PHO) Report classification/justification of - Medicines belonging to the ATC group M01 (Antiinflammatory and antirheumatic products) Table of Contents Page INTRODUCTION 6 DISCLAIMER 8 GLOSSARY OF TERMS USED IN THIS DOCUMENT 9 ACTIVE SUBSTANCES Phenylbutazone (ATC: M01AA01) 11 Mofebutazone (ATC: M01AA02) 17 Oxyphenbutazone (ATC: M01AA03) 18 Clofezone (ATC: M01AA05) 19 Kebuzone (ATC: M01AA06) 20 Indometacin (ATC: M01AB01) 21 Sulindac (ATC: M01AB02) 25 Tolmetin (ATC: M01AB03) 30 Zomepirac (ATC: M01AB04) 33 Diclofenac (ATC: M01AB05) 34 Alclofenac (ATC: M01AB06) 39 Bumadizone (ATC: M01AB07) 40 Etodolac (ATC: M01AB08) 41 Lonazolac (ATC: M01AB09) 45 Fentiazac (ATC: M01AB10) 46 Acemetacin (ATC: M01AB11) 48 Difenpiramide (ATC: M01AB12) 53 Oxametacin (ATC: M01AB13) 54 Proglumetacin (ATC: M01AB14) 55 Ketorolac (ATC: M01AB15) 57 Aceclofenac (ATC: M01AB16) 63 Bufexamac (ATC: M01AB17) 67 2 Indometacin, Combinations (ATC: M01AB51) 68 Diclofenac, Combinations (ATC: M01AB55) 69 Piroxicam (ATC: M01AC01) 73 Tenoxicam (ATC: M01AC02) 77 Droxicam (ATC: M01AC04) 82 Lornoxicam (ATC: M01AC05) 83 Meloxicam (ATC: M01AC06) 87 Meloxicam, Combinations (ATC: M01AC56) 91 Ibuprofen (ATC: M01AE01) 92 Naproxen (ATC: M01AE02) 98 Ketoprofen (ATC: M01AE03) 104 Fenoprofen (ATC: M01AE04) 109 Fenbufen (ATC: M01AE05) 112 Benoxaprofen (ATC: M01AE06) 113 Suprofen (ATC: M01AE07) 114 Pirprofen (ATC: M01AE08) 115 Flurbiprofen (ATC: M01AE09) 116 Indoprofen (ATC: M01AE10) 120 Tiaprofenic Acid (ATC:
    [Show full text]
  • Use of Antibiotics and Probiotics Reduces the Risk of Metachronous Gastric Cancer After Endoscopic Resection
    biology Article Use of Antibiotics and Probiotics Reduces the Risk of Metachronous Gastric Cancer after Endoscopic Resection Junya Arai 1 , Ryota Niikura 1,2,* , Yoku Hayakawa 1,* , Takuya Kawahara 3, Tetsuro Honda 4, Kenkei Hasatani 5, Naohiro Yoshida 6, Tsutomu Nishida 7 , Tetsuya Sumiyoshi 8, Shu Kiyotoki 9, Takashi Ikeya 10, Masahiro Arai 11, Nobumi Suzuki 1, Yosuke Tsuji 1, Atsuo Yamada 1, Takashi Kawai 2 and Kazuhiko Koike 1 1 Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8655, Japan; [email protected] (J.A.); [email protected] (N.S.); [email protected] (Y.T.); [email protected] (A.Y.); [email protected] (K.K.) 2 Department of Gastroenterological Endoscopy, Tokyo Medical University, Shinjuku-ku, Tokyo 160-0023, Japan; [email protected] 3 Clinical Research Promotion Center, The University of Tokyo Hospital, Tokyo 113-8655, Japan; [email protected] 4 Department of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki-shi, Nagasaki 850-8555, Japan; [email protected] 5 Department of Gastroenterology, Fukui Prefectural Hospital, Fukui-shi, Fukui 910-0846, Japan; [email protected] 6 Department of Gastroenterology, Ishikawa Prefectural Central Hospital, Kanazawa-shi, Ishikawa 920-8530, Japan; [email protected] 7 Department of Gastroenterology, Toyonaka Municipal Hospital, Toyonaka-shi, Osaka 560-8565, Japan; Citation: Arai, J.; Niikura, R.; [email protected] 8 Hayakawa, Y.; Kawahara, T.; Honda, Department of Gastroenterology, Tonan Hospital, Sapporo-shi, Hokkaido 060-0004, Japan; [email protected] T.; Hasatani, K.; Yoshida, N.; Nishida, 9 Department of Gastroenterology, Shuto General Hospital, Yanai-shi, Yamaguchi 333-0801, Japan; T.; Sumiyoshi, T.; Kiyotoki, S.; et al.
    [Show full text]
  • Ep 2002846 B1
    (19) TZZ ZZ _T (11) EP 2 002 846 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.: of the grant of the patent: A61K 45/06 (2006.01) A61K 38/20 (2006.01) 25.01.2017 Bulletin 2017/04 A61K 31/519 (2006.01) A61K 31/505 (2006.01) (21) Application number: 08014990.9 (22) Date of filing: 08.12.1997 (54) Combination therapy using an IL-1 inhibitor for treating IL-1 mediated diseases Kombinationstherapie mit einem IL-1-Inhibitor zur Behandlung von IL-1-vermittelten Krankheiten Thérapie combinée utilisant un inhibiteur IL-1 pour traiter les maladies liées au IL-1 (84) Designated Contracting States: • M. BRODY ET AL.: "MECHANISM OF ACTION OF AT BE CH DE DK ES FI FR GB GR IE IT LI LU MC METHOTREXATE: EXPERIMENTAL EVIDENCE NL PT SE THAT METHOTREXATE BLOCKS THE BINDING Designated Extension States: OF INTERLEUKIN 1 BETA TO THE INTERLEUKIN AL LT LV MK RO SI 1 RECEPTOR ON TARGET CELLS." EUROPEAN JOURNAL OF CLINICAL CHEMISTRY AND (30) Priority: 06.12.1996 US 32790 P CLINICAL BIOCHEMISTRY, vol. 31, no. 10, 23.01.1997 US 36353 P October 1993 (1993-10), pages 667-674, 07.02.1997 US 39311 P XP002062344 BERLIN, DE 09.07.1997 US 52025 P • M. SEITZ ET AL.: "METHOTREXATE ACTION IN RHEUMATOID ARTHRITIS: STIMULATION OF (43) Date of publication of application: CYTOKINE INHIBITOR AND INHIBITION OF 17.12.2008 Bulletin 2008/51 CHEMOKINE PRODUCTION BY PERIPHERAL BLOOD MONONUCLEAR CELLS." BRITISH (62) Document number(s) of the earlier application(s) in JOURNAL OF RHEUMATOLOGY, vol.
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 8.242,146 B2 Klein Et Al
    USOO8242146 B2 (12) United States Patent (10) Patent No.: US 8.242,146 B2 Klein et al. (45) Date of Patent: Aug. 14, 2012 (54) COMBINATION OF ANSAID AND A PDE-4 Wolda, S.L., “PDE4 inhibitors and chronic obstructive pulmonary INHIBITOR disease”, Emerging Drugs, vol. 5, No. 3, pp. 309-319, (2000). Silva, J.C.R. et al., “Effects of pentoxifylline and nabumetone on the (75) Inventors: Thomas Klein, Constance (DE); serum levels of IL-1B and TNF C in rats with adjuvant arthritis', Hans-Peter Kley, Allensbach (DE) Inflammation Research, vol. 49, pp. 14-19, (2000). Kumar, A. et al., “Analgesic and anti-inflammatory effects of (73) Assignee: Nycomed GmbH, Constance (DE) phosphodiesterase inhibitors'. Indian Journal of Experimental Biol ogy, vol. 38, pp. 26-30. (2000). (*) Notice: Subject to any disclaimer, the term of this Reuter, B.K. et al., “Phosphodiesterase inhibitors prevent NSAID patent is extended or adjusted under 35 entreopathy independently of effects on TNF-C. release'. Am J U.S.C. 154(b) by 1207 days. Physiol, vol. 277, pp. G847-G854, (1999). Sivola, J. et al., “Effects of nonsteroidal anti-inflammatory drugs on (21) Appl. No.: 12/003,129 rat gastric mucosal phosphodiesterase activity'. Agents and Actions, vol. 12, No. 4, pp. 516-520, (1982). (22) Filed: Dec. 20, 2007 Salcedo, J. et al., “Phosphodiesterase 4 Inhibition, A New Mecha nism to Maintain and Promote Gastric and Intestinal Mucosal Integ (65) Prior Publication Data rity Against NSAID-Induced Injury in the Rat', Gastroenterology, US 2008/O255.209 A1 Oct. 16, 2008 vol. 114, No.
    [Show full text]