DEFITELIO® Defibrotide

Total Page:16

File Type:pdf, Size:1020Kb

DEFITELIO® Defibrotide This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. You can report side effects to your doctor, or directly at www.tga.gov.au/reporting-problems. DEFITELIO® defibrotide Consumer Medicine Information What is in this leaflet This medicine can be used in adults, • have heavy bleeding and need a and in adolescents, children and blood transfusion This leaflet answers some common infants over one month of age. • are undergoing surgery questions about DEFITELIO. It Ask your doctor if you have any • have problems with blood does not contain all the available questions about why this circulation because your body information. It does not take the medicine has been prescribed for cannot maintain a constant place of talking to your doctor. you. blood pressure. All medicines have risks and This medicine is available only with DEFITELIO is not recommended in benefits. Your doctor has weighed a doctor's prescription. children less than 1 month of age. the risks of you using DEFITELIO This medicine is not expected to If you are not sure if you should against the benefits they expect it affect your ability to drive a car or be given DEFITELIO talk to your will have for you. operate machinery. doctor. If you have any concerns about using this medicine, ask your Taking other medicines doctor. Tell your doctor if you are taking Keep this leaflet. Before you are given any other medicines including You may need to read it again. DEFITELIO medicines that you buy without a prescription from your When you must not be given pharmacy, supermarket or health this medicine food shop. What DEFITELIO is Tell your doctor if you are taking used for You must not be given DEFITELIO any of the following: if you: • medicines to break down blood DEFITELIO is a medicine that • are allergic to defibrotide or any clots, such as tissue contains the active substance of the other ingredients listed in plasminogen activators (e.g. defibrotide. this leaflet alteplase, reteplase). DEFITELIO is used to treat a • are using other medicines to • medicines used to thin your condition called hepatic veno- break down blood clots such as blood such as aspirin, heparin occlusive disease (or VOD), in tissue plasminogen activators sodium, warfarin, dabigatran which the blood vessels in the liver (e.g. alteplase, reteplase). etexilate, rivaroxaban, apixaban become damaged and obstructed by • non-steroidal anti-inflammatory Before you are given this blood clots. This can be caused by medicines such as ibuprofen, medicines that are given prior to a medicine naproxen, diclofenac and other stem cell transplantation. Tell your doctor if you have nonsteroidal anti-inflammatory DEFITELIO works by protecting allergies to any other medicines, medicines. the cells of the blood vessels and foods, preservatives or dyes. preventing or breaking down the Tell your doctor if you: blood clots. • are taking medicine that thins your blood or increases the risk of bleeding DEFITELIO® Published by MIMS December 2020 1 Pregnancy When it is given • bleeding from the infusion line or catheter If you are pregnant, think you You will receive this treatment four • bleeding at the site of injection may be pregnant or are planning times a day for at least 21 days or to have a baby, tell your doctor. until your symptoms resolve. • bleeding from the mouth Defitelio should not be used during • bleeding from the eye pregnancy unless there is a definite If you miss a dose • chest pain need. Your doctor will discuss with Tell your doctor or nurse • shortness of breath you the risk and benefit involved in immediately if you think you have • rapid heart beat using DEFITELIO during missed a dose of DEFITELIO. pregnancy. • fever or high temperature As you will be given this medicine • dizziness or light-headedness If you are sexually active and you by a doctor or a nurse it is unlikely • sudden signs of allergy such as or your partner could become that a dose will be missed. You pregnant, you both must use rash, itching or hives on the must not be given a double dose to effective contraception during skin, swelling of the face, lips, make up for a missed dose. treatment with DEFITELIO and tongue or other parts of the for 1 week after stopping the If you are given too much body, shortness of breath, treatment. wheezing or trouble breathing. (overdose) • feeling sick, also called nausea Breastfeeding As DEFITELIO is given to you • vomiting under the supervision of your doctor If you are breastfeeding, tell your • diarrhoea doctor. it is unlikely that you will be given • rash Your doctor can discuss with you too much. However, if you the risk and benefits involved. experience any side effects after • red or purple, flat, pinhead spots under the skin If you have not told your doctor being given DEFITELIO, tell your about any of the above, tell doctor immediately. • itching. him/her before you are given Other side effects not listed above DEFITELIO. may also occur in some people. Side effects How DEFITELIO is Like all medicines, DEFITELIO After you are given given can cause side effects, although not DEFITELIO everybody gets them. Your doctor will discuss these with you and The treatment with DEFITELIO Storage can be initiated and continuously explain the risks and benefits of supervised only by an experienced your treatment. It is unlikely that you will be asked doctor in a hospital or in a Ask your doctor or pharmacist to to store DEFITELIO yourself. It specialised centre for stem cell answer any questions you may will usually be stored in the transplantation. have. pharmacy or on the ward. Tell your doctor or nurse DEFITELIO is stored below 25°C. How much is given immediately if you notice any of It must not be frozen. the following as you may require The total dose of DEFITELIO that Keep this medicine out of reach medical attention: is given is calculated based on your and sight of children. body weight. The calculation of the • signs of increased or unusual Do not use DEFITELIO after the dose in children from one month to bleeding or bruising during or expiry date which is stated on the 18 years of age is the same as in after treatment carton and vial label after ‘EXP’. adults. • nosebleeds The expiry date refers to the last • passing of blood in the urine or day of the month. How it is given faeces DEFITELIO will be given via a • dark coloured faeces drip (a slow injection into your • bloody diarrhoea veins) over a 2-hour period. This is • vomiting blood or material that also called an intravenous infusion. looks like coffee grounds DEFITELIO® Published by MIMS December 2020 2 Product description What it looks like DEFITELIO is a clear light yellow to brown concentrated solution for infusion, free from particulate matter or turbidity. One carton contains 10 glass vials, each with 2.5 mL of concentrated solution for infusion. Ingredients The active substance in DEFITELIO is defibrotide. Each 2.5 mL vial contains 200 mg defibrotide and each mL of concentrated solution contains 80 mg defibrotide. DEFITELIO also contains: • sodium citrate dihydrate • hydrochloric acid • sodium hydroxide • water for injections. Name and address of the sponsor DEFITELIO is distributed in Australia by: Link Medical Products Pty Ltd 5 Apollo Street Warriewood NSW 2102 AUSTRALIA Australian registration number: AUST R 319221 Date of preparation July 2020. DEFITELIO® Published by MIMS December 2020 3.
Recommended publications
  • Characterising the Risk of Major Bleeding in Patients With
    EU PE&PV Research Network under the Framework Service Contract (nr. EMA/2015/27/PH) Study Protocol Characterising the risk of major bleeding in patients with Non-Valvular Atrial Fibrillation: non-interventional study of patients taking Direct Oral Anticoagulants in the EU Version 3.0 1 June 2018 EU PAS Register No: 16014 EMA/2015/27/PH EUPAS16014 Version 3.0 1 June 2018 1 TABLE OF CONTENTS 1 Title ........................................................................................................................................... 5 2 Marketing authorization holder ................................................................................................. 5 3 Responsible parties ................................................................................................................... 5 4 Abstract ..................................................................................................................................... 6 5 Amendments and updates ......................................................................................................... 7 6 Milestones ................................................................................................................................. 8 7 Rationale and background ......................................................................................................... 9 8 Research question and objectives .............................................................................................. 9 9 Research methods ....................................................................................................................
    [Show full text]
  • Drug Consumption in 2017 - 2020
    Page 1 Drug consumption in 2017 - 2020 2020 2019 2018 2017 DDD/ DDD/ DDD/ DDD/ 1000 inhab./ Hospital 1000 inhab./ Hospital 1000 inhab./ Hospital 1000 inhab./ Hospital ATC code Subgroup or chemical substance day % day % day % day % A ALIMENTARY TRACT AND METABOLISM 322,79 3 312,53 4 303,08 4 298,95 4 A01 STOMATOLOGICAL PREPARATIONS 14,28 4 12,82 4 10,77 6 10,46 7 A01A STOMATOLOGICAL PREPARATIONS 14,28 4 12,82 4 10,77 6 10,46 7 A01AA Caries prophylactic agents 11,90 3 10,48 4 8,42 5 8,45 7 A01AA01 sodium fluoride 11,90 3 10,48 4 8,42 5 8,45 7 A01AA03 olaflur 0,00 - 0,00 - 0,00 - 0,00 - A01AB Antiinfectives for local oral treatment 2,36 8 2,31 7 2,31 7 2,02 7 A01AB03 chlorhexidine 2,02 6 2,10 7 2,09 7 1,78 7 A01AB11 various 0,33 21 0,21 0 0,22 0 0,24 0 A01AD Other agents for local oral treatment 0,02 0 0,03 0 0,04 0 - - A01AD02 benzydamine 0,02 0 0,03 0 0,04 0 - - A02 DRUGS FOR ACID RELATED DISORDERS 73,05 3 71,13 3 69,32 3 68,35 3 A02A ANTACIDS 2,23 1 2,22 1 2,20 1 2,30 1 A02AA Magnesium compounds 0,07 22 0,07 22 0,08 22 0,10 19 A02AA04 magnesium hydroxide 0,07 22 0,07 22 0,08 22 0,10 19 A02AD Combinations and complexes of aluminium, 2,17 0 2,15 0 2,12 0 2,20 0 calcium and magnesium compounds A02AD01 ordinary salt combinations 2,17 0 2,15 0 2,12 0 2,20 0 A02B DRUGS FOR PEPTIC ULCER AND 70,82 3 68,91 3 67,12 3 66,05 4 GASTRO-OESOPHAGEAL REFLUX DISEASE (GORD) A02BA H2-receptor antagonists 0,17 7 0,74 4 1,10 4 1,11 5 A02BA02 ranitidine 0,00 1 0,63 3 0,99 3 0,99 4 A02BA03 famotidine 0,16 7 0,11 8 0,11 10 0,12 9 A02BB Prostaglandins 0,04 62
    [Show full text]
  • Pharmacokinetic Profile of Defibrotide in Patients with Renal Impairment
    Journal name: Drug Design, Development and Therapy Article Designation: Clinical Trial Report Year: 2016 Volume: 10 Drug Design, Development and Therapy Dovepress Running head verso: Tocchetti et al Running head recto: Pharmacokinetic profile of defibrotide in renal impairment open access to scientific and medical research DOI: http://dx.doi.org/10.2147/DDDT.S112181 Open Access Full Text Article CLINICAL TRIAL REPORT Pharmacokinetic profile of defibrotide in patients with renal impairment Paola Tocchetti1 Abstract: Hepatic veno-occlusive disease, also called sinusoidal obstruction syndrome (VOD/ Elena Tudone2 SOS), is an unpredictable, potentially life-threatening complication of hematopoietic stem cell Jean-Francois Marier3 transplant conditioning. Severe VOD/SOS, generally associated with multiorgan dysfunction Thomas C Marbury4 (pulmonary or renal dysfunction), may be associated with .80% mortality. Defibrotide, recently Katie Zomorodi5 approved in the US, has demonstrated efficacy treating hepatic VOD/SOS with multiorgan Mark Eller6 dysfunction. Because renal impairment is prevalent in patients with VOD/SOS, this Phase I, open-label, two-part study in adults examined the effects of hemodialysis and severe or end-stage 1 2 Gentium, Clinical Operations, renal disease (ESRD) on defibrotide pharmacokinetics (PK). Part 1 compared defibrotide PK Gentium, Villa Guardia, Como, Italy; 3Reporting and Analysis Services, during single 6.25 mg/kg doses infused with and without dialysis. Part 2 assessed defibrotide Pharsight, a Certara Company, plasma PK after multiple 6.25 mg/kg doses in nondialysis-dependent subjects with severe/ Montreal, Quebec, Canada; 4Orlando ESRD versus healthy matching subjects. Among six subjects enrolled in Part 1, percent ratios Clinical Research Center, Orlando, FL, 5 For personal use only.
    [Show full text]
  • Tracking Form for Applicants for New Technology Add-On Payments Under the Acute Inpatient Prospective Payment System (IPPS) for Federal Fiscal Year (FY) 2017
    Centers for Medicare & Medicaid Services Center for Medicare Management 7500 Security Boulevard Baltimore, Maryland 21244-1850 Tracking Form for Applicants for New Technology Add-on Payments under the Acute Inpatient Prospective Payment System (IPPS) for Federal Fiscal Year (FY) 2017 1. Technology Name: Titan Spine Endoskeleton® nanoLOCK™ Interbody Device 2. Manufacturer Name: Titan Spine 3. Trade Brand of Technology: Titan Spine Endoskeleton® nanoLOCK™ 4. Brief Description of Service, Device or Drug: The nanoLOCK™ is a nanotechnology-based interbody medical device with a dual acid-etched titanium interbody system to treat patients with degenerative disc disease. One of the key distinguishing features is the surface manufacturing technique and materials which produce macro, micro, and nano surface textures. The unique combination of surface topographies enable initial implant fixation, mimic an osteoclastic pit for bone growth, and especially produce the nano­ scale features that interface with the integrins on the outside of the cellular membrane. These generate better osteogenic and angiogenic responses that enhance bone growth, fusion and stability. nanoLOCK™’s clinical features also reduce pain, improve recovery time, lower rates of device complications such as debris and inflammation. Centers for Medicare & Medicaid Services Center for Medicare Management 7500 Security Boulevard Baltimore, Maryland 21244-1850 Tracking Form for Applicants for New Technology Add-on Payments under the Acute Inpatient Prospective Payment System (IPPS) for Federal Fiscal Year (FY) 2017 1. Technology Name: defibrotide 2. Manufacturer Name: Jazz Pharmaceuticals, Inc. 3. Trade Brand of Technology: Defitelio®. The trade brand name of Defitelio for defibrotide has been conditionally approved by the United States (US) Food and Drug Administration (FDA) and is subject to FDA confirmation in connection with approval of the New Drug Application (NDA).
    [Show full text]
  • Defibrotide for the Treatment and Prophylaxis of Hepatic Veno-Occlusive Disease
    Defibrotide for the treatment and prophylaxis of hepatic veno-occlusive disease Systematic Review Decision Support Document No. 84 ISSN online: 1998-0469 Defibrotide for the treatment and prophylaxis of hepatic veno-occlusive disease Systematic Review Vienna, March 2015 Project Team Project Leader: Dr. med. Anna Nachtnebel, MSc Authors: Dr. med. Eleen Rothschedl Dr. med. Anna Nachtnebel, MSc Internal Review: Dr. rer.nat. Agnes Kisser Project Support Systematic Literature Search: Tarquin Mittermayr, BA External Review: Prof. Dr. med. Wolfgang Bethge Medizinische Universitätsklinik II Hämatologie/Onkologie Allogene Stammzelltransplantation Universitätsklinikum Tübingen Correspondence Dr. med. Eleen Rothschedl, e-mail: [email protected] This report should be referenced as follows: Rothschedl E., Nachtnebel A. Defibrotide for the treatment and prophylaxis of hepatic veno-occlusive disease. Decision Support Document No. 84; 2015. Vienna: Ludwig Boltzmann Institute for Health Technology Assessment. Conflict of interest All authors and reviewers involved in the production of this report have declared they have no conflicts of interest in relation to the technology assessed according to the Uniform Requirements of Manuscripts Statement of Medical Journal Editors (www.icmje.org). Commissioned by the Austrian Ministry of Health, this report systematically assessed the intervention described herein as decision support for the inclusion in the catalogue of benefits. CONTENT INFORMATION Publisher: Ludwig Boltzmann Gesellschaft GmbH Nußdorferstr. 64, 6 Stock, A-1090 Wien http://www.lbg.ac.at/de/lbg/impressum Responsible for content: Ludwig Boltzmann Institute for Health Technology Assessment (LBI-HTA) Garnisongasse 7/20, A-1090 Vienna http://hta.lbg.ac.at/ Decision support documents of the LBI-HTA do not appear on a regular basis and serve to publicize the research results of the Ludwig Boltzmann Institute of Health Technology Assessments.
    [Show full text]
  • Antithrombotic Agents in the Management of Sepsis
    Antithrombotic Agents in the Management of Sepsis !"#$ Loyola University Medical Center, Maywood, Illinois-60153, USA ABSTRACT Sepsis, a systemic inflammatory syndrome, is a response to infection and when associated with mul- tiple organ dysfunction is termed, severe sepsis. It remains a leading cause of mortality in the critically ill. The response to the invading bacteria may be considered as a balance between proinflammatory and antiinflammatory reaction. While an inadequate proinflammatory reaction and a strong antiinflammatory response could lead to overwhelming infection and death of the patient, a strong and uncontrolled pro- inflammatory response, manifested by the release of proinflammatory mediators may lead to microvas- cular thrombosis and multiple organ failure. Endotoxin triggers sepsis by releasing various mediators inc- luding tumor necrosis factor-alpha and interleukin-1(IL-1). These cytokines activate the complement and coagulation systems, release adhesion molecules, prostaglandins, leukotrienes, reactive oxygen speci- es and nitric oxide (NO). Other mediators involved in the sepsis syndrome include IL-1, IL-6 and IL-8; arachidonic acid metabolites; platelet activating factor (PAF); histamine; bradykinin; angiotensin; comp- lement components and vasoactive intestinal peptide. These proinflammatory responses are counterac- ted by IL-10. Most of the trials targeting the different mediators of proinflammatory response have failed due a lack of correct definition of sepsis. Understanding the exact pathophysiology of the disease will enable better treatment options. Targeting the coagulation system with various anticoagulant agents inc- luding antithrombin, activated protein C (APC), tissue factor pathway inhibitor (TFPI) is a rational appro- ach. Many clinical trials have been conducted to evaluate these agents in severe sepsis.
    [Show full text]
  • Antiplatelet Agents for Chronic Kidney Disease
    bs_bs_banner Nephrology 18 (2013) 474–476 COCHRANE COMMENTARIES Edited by Angela Webster ([email protected]) Written by Suetonia Palmer, Valeria Saglimbene and Giovanni FM Strippoli ([email protected]) Antiplatelet agents for chronic kidney disease What is in this review about? patients) were conducted in people who had an acute coro- nary syndrome or who were undergoing percutaneous inter- This systematic review summarized the randomized trials vention and examined glycoprotein IIb/IIIa inhibitors evaluating the benefits and harms of antiplatelet agents (abciximab, tirofiban or eptifibatide) with or without clopi- (including aspirin, dipyridamole, thienopyridines (clopidog- dogrel in addition to aspirin and heparin in the setting of rel, ticlopidine), defibrotide, picotamide, sulfinpyrazone, and chronic kidney disease stage 3–5. For these interventions, glycoprotein IIb/IIIa inhibitors (abciximab, tirofiban and data were entirely based on post-hoc analysis for the sub- eptifibatide)) in addition to standard treatment in people group with chronic kidney disease derived from larger trials. who have chronic kidney disease. We focus here on evidence The remaining trials examined oral antiplatelet therapy in of major cardiovascular events, mortality and bleeding. people who have chronic kidney disease (aspirin, thienopy- ridines or dipyridamole, defibrotide, picotamide, or sulfin- What are the key findings? pyrazone alone or in combination) and who were at risk of or who had stable cardiovascular disease. Overall, 19 studies In
    [Show full text]
  • PRAC Draft Agenda of Meeting 11-14 May 2020
    11 May 2020 EMA/PRAC/257460/2020 Human Division Pharmacovigilance Risk Assessment Committee (PRAC) Draft agenda for the meeting on 11-14 May 2020 Chair: Sabine Straus – Vice-Chair: Martin Huber 11 May 2020, 10:30 – 19:30, via teleconference 12 May 2020, 08:30 – 19:30, via teleconference 13 May 2020, 08:30 – 19:30, via teleconference 14 May 2020, 08:30 – 16:00, via teleconference Organisational, regulatory and methodological matters (ORGAM) 28 May 2020, 09:00-12:00, via teleconference Disclaimers Some of the information contained in this agenda is considered commercially confidential or sensitive and therefore not disclosed. With regard to intended therapeutic indications or procedure scopes listed against products, it must be noted that these may not reflect the full wording proposed by applicants and may also change during the course of the review. Additional details on some of these procedures will be published in the PRAC meeting highlights once the procedures are finalised. Of note, this agenda is a working document primarily designed for PRAC members and the work the Committee undertakes. Note on access to documents Some documents mentioned in the agenda cannot be released at present following a request for access to documents within the framework of Regulation (EC) No 1049/2001 as they are subject to on-going procedures for which a final decision has not yet been adopted. They will become public when adopted or considered public according to the principles stated in the Agency policy on access to documents (EMA/127362/2006, Rev. 1). Official address Domenico Scarlattilaan 6 ● 1083 HS Amsterdam ● The Netherlands Address for visits and deliveries Refer to www.ema.europa.eu/how-to-find-us Send us a question Go to www.ema.europa.eu/contact Telephone +31 (0)88 781 6000 An agency of the European Union © European Medicines Agency, 2020.
    [Show full text]
  • Injectable Medication Hcpcs/Dofr Crosswalk
    INJECTABLE MEDICATION HCPCS/DOFR CROSSWALK HCPCS DRUG NAME GENERIC NAME PRIMARY CATEGORY SECONDARY CATEGORY J0287 ABELCET Amphotericin B lipid complex THERAPEUTIC INJ HOME HEALTH/INFUSION** J0400 ABILIFY Aripiprazole, intramuscular, 0.25 mg THERAPEUTIC INJ J0401 ABILIFY MAINTENA Apriprazole 300mg, IM injection THERAPEUTIC INJ J9264 ABRAXANE paclitaxel protein-bound particles, 1 mg J1120 ACETAZOLAMIDE SODIUM Acetazolamide sodium injection THERAPEUTIC INJ J0132 ACETYLCYSTEINE INJ Acetylcysteine injection, 10 mg THERAPEUTIC INJ ACTEMRA 162mg/0.9ml Syringe (50242- J3262 SELF-INJECTABLE 0138-01) Tocilizumab, 1 mg ACTEMRA INJECTION (50242-0136-01, J3262 50242-0137-01) Tocilizumab 200mg, 400mg THERAPEUTIC INJ J0800 ACTHAR HP Corticotropin injection THERAPEUTIC INJ Hemophilus influenza b vaccine (Hib), PRP-T conjugate (4- 90648 ACTHIB dose schedule), for intramuscular use THERAPEUTIC INJ IMMUNIZATIONS J0795 ACTHREL Corticorelin ovine triflutal THERAPEUTIC INJ J9216 ACTIMMUNE Interferon gamma 1-b 3 miillion units SELF-INJECTABLE CHEMO ADJUNCT* J2997 ACTIVASE Alteplase recombinant, 1mg THERAPEUTIC INJ HOME HEALTH/INFUSION** J0133 ACYCLOVIR SODIUM Acyclovir, 5 mg THERAPEUTIC INJ HOME HEALTH/INFUSION** 90715 ADACEL Tdap vaccine, > 7 yrs, IM THERAPEUTIC INJ IMMUNIZATIONS J2504 ADAGEN Pegademase bovine, 25 IU THERAPEUTIC INJ HOME HEALTH/INFUSION** J9042 ADCETRIS Brentuximab vedotin Injection THERAPEUTIC INJ CHEMOTHERAPY J0153 ADENOCARD Adenosine 6 MG THERAPEUTIC INJ J0171 ADRENALIN Adrenalin (epinephrine) inject THERAPEUTIC INJ J9000 ADRIAMYCIN Doxorubicin
    [Show full text]
  • Drug Consumption at Wholesale Prices in 2017 - 2020
    Page 1 Drug consumption at wholesale prices in 2017 - 2020 2020 2019 2018 2017 Wholesale Hospit. Wholesale Hospit. Wholesale Hospit. Wholesale Hospit. ATC code Subgroup or chemical substance price/1000 € % price/1000 € % price/1000 € % price/1000 € % A ALIMENTARY TRACT AND METABOLISM 321 590 7 309 580 7 300 278 7 295 060 8 A01 STOMATOLOGICAL PREPARATIONS 2 090 9 1 937 7 1 910 7 2 128 8 A01A STOMATOLOGICAL PREPARATIONS 2 090 9 1 937 7 1 910 7 2 128 8 A01AA Caries prophylactic agents 663 8 611 11 619 12 1 042 11 A01AA01 sodium fluoride 610 8 557 12 498 15 787 14 A01AA03 olaflur 53 1 54 1 50 1 48 1 A01AA51 sodium fluoride, combinations - - - - 71 1 206 1 A01AB Antiinfectives for local oral treatment 1 266 10 1 101 6 1 052 6 944 6 A01AB03 chlorhexidine 930 6 885 7 825 7 706 7 A01AB11 various 335 21 216 0 227 0 238 0 A01AB22 doxycycline - - 0 100 0 100 - - A01AC Corticosteroids for local oral treatment 113 1 153 1 135 1 143 1 A01AC01 triamcinolone 113 1 153 1 135 1 143 1 A01AD Other agents for local oral treatment 49 0 72 0 104 0 - - A01AD02 benzydamine 49 0 72 0 104 0 - - A02 DRUGS FOR ACID RELATED DISORDERS 30 885 4 32 677 4 35 102 5 37 644 7 A02A ANTACIDS 3 681 1 3 565 1 3 357 1 3 385 1 A02AA Magnesium compounds 141 22 151 22 172 22 155 19 A02AA04 magnesium hydroxide 141 22 151 22 172 22 155 19 A02AD Combinations and complexes of aluminium, 3 539 0 3 414 0 3 185 0 3 231 0 calcium and magnesium compounds A02AD01 ordinary salt combinations 3 539 0 3 414 0 3 185 0 3 231 0 A02B DRUGS FOR PEPTIC ULCER AND 27 205 5 29 112 4 31 746 5 34 258 8
    [Show full text]
  • Estonian Statistics on Medicines 2013 1/44
    Estonian Statistics on Medicines 2013 DDD/1000/ ATC code ATC group / INN (rout of admin.) Quantity sold Unit DDD Unit day A ALIMENTARY TRACT AND METABOLISM 146,8152 A01 STOMATOLOGICAL PREPARATIONS 0,0760 A01A STOMATOLOGICAL PREPARATIONS 0,0760 A01AB Antiinfectives and antiseptics for local oral treatment 0,0760 A01AB09 Miconazole(O) 7139,2 g 0,2 g 0,0760 A01AB12 Hexetidine(O) 1541120 ml A01AB81 Neomycin+Benzocaine(C) 23900 pieces A01AC Corticosteroids for local oral treatment A01AC81 Dexamethasone+Thymol(dental) 2639 ml A01AD Other agents for local oral treatment A01AD80 Lidocaine+Cetylpyridinium chloride(gingival) 179340 g A01AD81 Lidocaine+Cetrimide(O) 23565 g A01AD82 Choline salicylate(O) 824240 pieces A01AD83 Lidocaine+Chamomille extract(O) 317140 g A01AD86 Lidocaine+Eugenol(gingival) 1128 g A02 DRUGS FOR ACID RELATED DISORDERS 35,6598 A02A ANTACIDS 0,9596 Combinations and complexes of aluminium, calcium and A02AD 0,9596 magnesium compounds A02AD81 Aluminium hydroxide+Magnesium hydroxide(O) 591680 pieces 10 pieces 0,1261 A02AD81 Aluminium hydroxide+Magnesium hydroxide(O) 1998558 ml 50 ml 0,0852 A02AD82 Aluminium aminoacetate+Magnesium oxide(O) 463540 pieces 10 pieces 0,0988 A02AD83 Calcium carbonate+Magnesium carbonate(O) 3049560 pieces 10 pieces 0,6497 A02AF Antacids with antiflatulents Aluminium hydroxide+Magnesium A02AF80 1000790 ml hydroxide+Simeticone(O) DRUGS FOR PEPTIC ULCER AND GASTRO- A02B 34,7001 OESOPHAGEAL REFLUX DISEASE (GORD) A02BA H2-receptor antagonists 3,5364 A02BA02 Ranitidine(O) 494352,3 g 0,3 g 3,5106 A02BA02 Ranitidine(P)
    [Show full text]
  • Antithrombotic Therapy in COVID-19: Systematic Summary of Ongoing Or Completed Randomized Trials
    medRxiv preprint doi: https://doi.org/10.1101/2021.01.04.21249227; this version posted January 6, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. Antithrombotic Therapy in COVID-19: Systematic Summary of Ongoing or Completed Randomized Trials Azita H. Talasaz, PharmD,1, 2 Parham Sadeghipour, MD,3 Hessam Kakavand, PharmD,1, 2 Maryam Aghakouchakzadeh, PharmD,1 Elaheh Kordzadeh-Kermani, PharmD,1 Benjamin W. Van Tassell, PharmD,4, 5 Azin Gheymati, PharmD,1 Hamid Ariannejad, MD,2 Seyed Hossein Hosseini, PharmD,1 Sepehr Jamalkhani, MD(2021),3 Michelle Sholzberg, MDCM, MSc,6, 7 Manuel Monreal, MD, PhD,8 David Jimenez, MD, PhD,9 Gregory Piazza, MD, MS,10 Sahil A. Parikh, MD,11, 12 Ajay J. Kirtane, MD, SM,11, 12 John W. Eikelboom, MBBS,13 Jean M. Connors, MD,14 Beverley J. Hunt, MD,15 Stavros V. Konstantinides MD, PhD,16, 17 Mary Cushman, MD, MSc18, 19 Jeffrey I. Weitz, MD,20, 21 Gregg W. Stone, MD,11, 22 Harlan M. Krumholz, MD, SM,23, 24, 25 Gregory Y.H. Lip, MD,26, 27 Samuel Z. Goldhaber, MD,10 and Behnood Bikdeli, MD, MS, 10, 11, 23, * Total Words Count: 9020 (including text, tables, Figure legends, but not online supplement) Affiliations: 1. Department of Clinical Pharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran. 2. Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran. 3. Cardiovascular Intervention Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
    [Show full text]