DOCSLIB.ORG

Package Leaflet: Information for the User Trampalgin 37.5 Mg/325 Mg

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Package Leaflet: Information for the User Trampalgin 37.5 Mg/325 Mg Package leaflet: Information for the user Trampalgin 37.5 mg/325 mg tablets tramadol hydrochloride/paracetamol Read all of this leaflet carefully before you start taking this medicine because it contains important information for you. • Keep this leaflet. You may need to read it again. • If you have any further questions, ask your doctor or pharmacist or nurse. • This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. • If you get any side effects, talk to your doctor or pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4. What is in this leaflet: 1. What Trampalgin is and what it is used for 2. What you need to know before you take Trampalgin 3. How to take Trampalgin 4. Possible side effects 5. How to store Trampalgin 6. Contents of the pack and other information 1. What Trampalgin is and what it is used for Trampalgin is composed of two pain relieving active substances, tramadol and paracetamol. Trampalgin is used to treat moderate to severe pain when your doctor recommends that a combination of tramadol and paracetamol is needed. Trampalgin is intended for adults, adolescents and children over 12 years of age. 2. What you need to know before you take Trampalgin Do not take Trampalgin • if you are allergic (hypersensitive) to the active substances tramadol and paracetamol or any of the other ingredients of Trampalgin • in cases of acute poisoning with alcohol, sleeping pills, pain relievers or psychotropic drugs (that affect mood, emotions and state of mind). • if you are also taking medicines called monoamine oxidase inhibitors (MAOIs) or have taken MAOIs in the last 14 days before treatment with Trampalgin. MAOIs are used in the treatment of depression or Parkinson’s disease. • if you have a severe liver disorder. • if you have epilepsy that is not adequately controlled by your current medicine. Warnings and precautions Take special care with Trampalgin if you 1/ 7 • take other medicines containing also active substances paracetamol or tramadol. • have liver disease as your eyes and skin may turn yellow, which may suggest jaundice. • have kidney problems. • have severe difficulties in breathing, for example asthma or severe lung problems. • have epilepsy or have already experienced fits or seizures. • have recently suffered from a head injury, shock or severe headaches associated with vomiting (being sick). • think you are addicted to other analgesics, for example morphine. • take other medicines to treat pain that contain buprenorphine, nalbuphine or pentazocine. • are going to have an anaesthetic (tell your doctor or dentist that you are taking Trampalgin). Should any of these problems occur during the treatment with Trampalgin or has it occurred in the past, inform your doctor. Please, pay attention to the fact that the active substance tramadol may induce physical or psychic dependence. The effect of tramadol may diminish with long-term use (the development of tolerance) and an increase in dosage may be needed. A treatment by Trampalgin of patients with drug-abusing tendencies or drug-dependent patients should be only for a short term under strict medical supervision. Children Trampalgin is not recommended in children under 12 years of age. Other medicines and Trampalgin Please inform your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. Trampalgin contains paracetamol and tramadol. Tell your doctor if you take any other medicine containing also paracetamol or tramadol. Do not exceed the total maximum daily doses of paracetamol or tramadol from this or other medicines. Do not take Trampalgin with MAOIs (see section Do not take Trampalgin). Trampalgin is not recommended with the following medicines: • carbamazepine (a medicine used to treat epilepsy or some types of pain) • buprenorphine, nalbuphine or pentazocine (opioid type pain relievers). Their pain relieving effect my be decreased. Trampalgin may increase the risk of side effects if you also take the following medicines: • medicines which may cause convulsions (fits), such as certain antidepressants,antipsycotics or bupropion. The risk of having a fit may increase if you take Trampalgin at the same time. Your doctor will tell you whether Trampalgin is suitable for you. • certain antidepressants such as selective serotonin re-uptake inhibitors (SSRIs) or triptans (used for migraine) . Trampalgin may interact with these medicines and you may experience symptoms such as involuntary, rhytmic contractions of muscles, including the muscles that control movement of the eye, agitation, excessive sweating, tremor, exaggeration of reflexes, increased muscle tension or body temperature above 38oC. 2/ 7 • tranquilizers, sleeping pills, other pain relievers such as morphine and codeine (also as cough medicine), baclofen (a muscle relaxant), medicines used to lower blood pressure, antidepressants or medicines to treat allergies. Check with your doctor if you feel drowsy or feel faint. • warfarin or phenprocoumon (for blood thinning). The effectiveness of such medicines may be altered and bleeding may occur (see section 4). Inform your doctor about any prolonged or unexpected bleeding. The effectiveness of Trampalgin may also be altered if you take the following medicines concomitantly: • metoclopramide, domperidone or ondansetron (medicines used to treat nausea and vomiting/being sick) • cholestyramine (medicine used to reduce cholesterol in the blood) • ketoconazole or erythromycin (medicines used against infections). Trampalgin with food and drink Do not drink alcohol while you are taking Trampalgin. Pregnancy, breast-feeding and fertility If you are pregnant or think you may be pregant, or if you are breast-feeding, ask your doctor for advice before taking any medicine. Do not take Trampalgin while you are pregnant. Inform your doctor if you become pregnant during treatment with Trampalgin. Trampalgin is not recommended while you are breastfeeding, as small amounts of tramadol may pass into the breast-milk. Driving and using machines If you feel drowsy while taking Trampalgin, do not drive, use tools or use machinery. 3. How to take Trampalgin Always take Trampalgin exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure. The dosage should be adjusted to the intensity of the pain and your individual pain sensitivity. In general the lowest pain-relieving dose should be taken. Take Trampalgin for as short a time as possible and no longer than your doctor has told you. Use in adults, adolescents and children over 12 years of age The recommended dosage is to start with 2 tablets, unless otherwise prescribed by your doctor. If required, further doses may be taken, as instructed by your doctor. The shortest time between doses must be at least 6 hours. Do not take more than 2 tablets in a single dose or 8 tablets per day. Your doctor may increase the time between doses: • if you are older than 75 years. 3/ 7 • if you have kidney problems. • if you have liver problems. Swallow the tablets whole with sufficient liquid. If you think that the effect of Trampalgin is too strong (you feel very drowsy or have difficulty breathing) or too weak (you do not have enough pain relief), contact your doctor. Use in children under 12 years of age Trampalgin is not recommended in children under 12 yers of age. Use in elderly patients In elderly patients (above 75 years) the excretion of tramadol may be delayed. If this applies to you, your doctor may recommend prolonging the dosage interval. Use in severe liver or kidney disease (insufficiency) patients Patients with severe liver and/or kidney insufficiency should not take Trampalgin. If in your case the insufficiency is mild or moderate, your doctor may recommend prolonging the dosage interval. If you take more Trampalgin than you should In case of overdose or accidentally taking this medicine by children seek immediately your doctor or the nearest hospital and tell them precisely what amount of this medicine was taken. Take all the remaining tablets and this package leaflet to your doctor. Overdose by paracetamol may cause serious impairment up to failure of liver function that may lead to death. If you forget to take Trampalgin If you forget to take the tablets, pain is likely to return. Do not take a double dose to make up for forgotten individual doses; simply continue taking the tablets as before. If you stop taking Trampalgin If you discontinue or abruptly interrupt the treatment with Trampalgin, the pain is likely to reappear. If you wish to discontinue the treatment due to the unpleasant side effects of the product, consult your doctor. The discontinuation of treatment with Trampalgin is not usually followed by withdrawal symptoms. After a discontinuation of long-term treatment, however, symptoms such as restlessness, anxiety, nervousness, panic attacks, hallucinations, unusual sensory sensations (itching, tingling, loss of sensation), tinnitus, insomnia, tremors or gastrointestinal symptoms may occur in some patients. Please contact your doctor, should any of these symptoms occur following the discontinuation of Trampalgin. If you have any further questions on the use of this product, ask your doctor or pharmacist. 4. Possible side effects Like all medicines, Trampalgin can have side effects although not everybody gets them. Some side effect could be serious.
Load more

Recommended publications
  • Aqualis ASA (A Public Limited Liability Company Organised Under the Laws of Norway) Org.No
    Aqualis ASA (A public limited liability company organised under the laws of Norway) Org.no. 913 757 424 The information in this prospectus (the "Prospectus") relates to (i) a underwritten rights issue (the “Rights Issue”) by Aqualis ASA (“Aqualis” or the “Company”, and when taken together with its consolidated subsidiaries, the “Group” or the “Aqualis Group”) and the listing on Oslo Børs of up to 8,882,575 new shares in the Company with a par value of NOK 0.1 each (the “Rights Issue Shares”), issued for a subscription price of NOK 3.96 per share (the “Subscription Price”), (ii) listing of 4,375,000 new shares in Aqualis, each with a par value of NOK 0.1 each (the “Private Placement Shares”) and (iii) listing of 14,865,621 new shares in Aqualis, each with a par value of NOK 0.1 each (the “Consideration Shares”, and together with the Rights Issue shares and the Private Placement Shares the “New Shares”). Subscription Period for the Rights Issue: From 24 June 09:00 (CET) to 8 July 16:30 (CET) Trading in Subscription Rights: From 24 09:00 (CET) 4 July 16:30 (CET) The shareholders of the Company as at 11 June 2019 (and being registered as such in the Norwegian Central Securities Depository (the "VPS") on 13 June 2019 pursuant to the two days' settlement procedure (the "Record Date")) (the "Existing Shareholders"), will be granted subscription rights in the Rights Issue that, subject to applicable law, provide preferential rights to subscribe for and be allocated Rights Issue Shares at the Subscription Price (the "Subscription Rights").
    [Show full text]
  • Aqualis Offshore Holding ASA (A Public Limited Liability Company Organised Under the Laws of Norway) Org.No
    Aqualis Offshore Holding ASA (A public limited liability company organised under the laws of Norway) Org.no. 913 757 424 Listing of 43,190,544 shares in Aqualis Offshore Holding ASA (the “Shares”) on the Oslo Stock Exchange (the “Listing”) The first day of listing of Aqualis Offshore Holding ASA (“New Aqualis” or the “Company”, together with its subsidiaries the “New Aqualis Group” or the “Group”) on the Oslo Stock Exchange is expected to be 13 August 2014 and trading in the shares will commence on the date of listing, under the trading symbol AQUA. Investing in the Shares involves a high degree of risk. See section 2 “Risk Factors” beginning on page 15. THIS PROSPECTUS SERVES AS A LISTING PROSPECTUS ONLY, AS REQUIRED BY NORWEGIAN LAW AND REGULATION. THIS PROSPECTUS DOES NOT CONSTITUE AN OFFER TO BUY, SUBSCRIBE OR SELL ANY OF THE SECURITIES DESCRIBED HEREIN, AND NO SECURITIES ARE BEING OFFERED OR SOLD PURSUANT TO IT. Manager: 12 August 2014 AQUALIS OFFSHORE HOLDING ASA IMPORTANT INFORMATION For the definitions of terms used throughout this Prospectus, see section 17 "Definitions and glossary of terms" of this Prospectus. This prospectus (the “Prospectus”) has been prepared to comply with the Norwegian Securities Trading Act of 29 June 2007 no. 75 (the “Norwegian Securities Trading Act”) and related secondary legislation, including the Commission Regulation (EC) no. 809/2004 implementing Directive 2003/71/EC of the European Parliament and of the Council of 4 November 2003 regarding information contained in prospectuses (the “Prospectus Directive”) as well as the format, incorporation by reference and publication of such prospectuses and dissemination of advertisements (hereafter “EC Regulation 809/2004”).
    [Show full text]
  • Let Food (Supplements) Be Thy Medicine
    4-Feb-19 7:40 AM Italian Equity Research PHARMANUTRA BUY Sector: Pharmaceutical New Coverage TP 21.50 Let Food (Supplements) Be Thy Medicine New Coverage Target price upside: +25% We initiate coverage on Pharmanutra with a BUY rating and a Target Price of EUR21.50 per FY18E FY19E share, providing 25% upside to the current share price. The Group is an undisputed leader in Change in EPS est. iron food supplements market (Sideral® has gained a 50% market share in Italy), and a 0.0% 0.0% credible challenger in the topical anti-inflammatory market (Cetilar® is quickly gaining market share). Thanks to an Intellectual Property (IP) production and management strategy Ticker (BBG, Reut) PHN IM PHN MI incomparable within the dietary supplements and medical devices industry, Pharmanutra Share price Ord. (Eu) 17.3 has created long-lasting competitive advantages and high barriers to protect its assets. The N. of Ord. shares (mn) 9.7 Group owns 8 proprietary raw materials, 7 patents based on pure technological innovation, Total N. of shares (mn) 9.7 25 registered brands, and has 79 completed clinical trials. We expect the impressive growth Market cap (Eu mn) 167 track record to continue in the medium term (we forecast a high-teens revenue and profit Total Market Cap (EU mn) 167 CAGR in 2017-20) driven by: the development of new formulations/applications for Sideral® Free Float Ord. (%) 29% and Cetilar® families of products, the launch of brand-new products (Sucrosomial Free Float Ord. (Eu mn) 48 magnesium®), and a wider penetration of foreign markets (the Group is constantly entering Daily AVG liquidity Ord.
    [Show full text]
  • Spec Pharma M&A Transaction Multiples
    SECTOR REPORT FOURTH QUARTER 2016 Disclaimer All information set forth in this report (the “Overview”) has been synthesized by Bourne Capital Partners, L.L.C. (“BP”) or was obtained from publicly available sources. BP makes no express or implied representation or warranty as to the accuracy or completeness of the information contained herein. BP expressly disclaims any and all liability that may be based on all information set forth in the Overview, errors therein, or omissions therefrom. This Overview includes certain statements, estimates and projections provided by BP with respect to anticipated future performance. Such statements, estimates and projections reflect various assumptions made by BP concerning anticipated results, which reflect significant subjective judgments made by BP and as a result, may or may not prove to be correct. There can be no assurance that such projected results are attainable or will be realized. No express or implied representations or warranties are made as to the accuracy of such statements, estimates or projections. In furnishing the Overview, BP does not undertake any obligation to provide the recipient with access to any additional information, to correct any inaccuracies that may become apparent or to update or otherwise revise this Overview. This Overview is not an offer to sell or a solicitation of an offer to purchase securities or to engage in any other transaction. BP is a North Carolina (USA) limited liability company doing business as Bourne Partners with divisions in Healthcare Merchant Banking, Alternative Assets, Management Consulting and Investment Banking. Investment Banking services are offered by Bourne Partners Securities, LLC, a registered broker dealer, Member FINRA and SIPC.
    [Show full text]
  • Smart Choices for Everyday Healthcare Annual Report 2019 Table of Contents
    Annual Report 2019 Smart choices for everyday healthcare Annual Report 2019 Table of contents 28 Multi-Gyn: Management A natural treatment Financial review for vaginal discomfort statements 29 Locobase: The international skin care brand from Karo Pharma 06 Smart choices for 38 Statutory administration everyday healthcare 30 Power to our people report 07 Business model and 32 Operation Smile: 50 Five-year summary key categories Combatting cleft lip and palate 52 Corporate governance 08 Strongholds in the Nordics report and a global presence 34 Share and shareholders 56 Board 10 Letter from the CEO: A new Karo Pharma 58 Management with a new purpose "We’ve made it our 68 Notes 12 Letter from the Chairman purpose to develop 93 Audit report 14 Growing through reliable ways for smart choices people to treat their 97 Annual general meeting 16 Highlights 2019 everyday ailments, 18 A new group to help them live at the reins healthier lives. We 20 Market overview: call it smart choices Growth drivers and challenges for everyday health- care." 24 M&A: The vehicle of our growth – Christoffer Lorenzen, CEO, Karo Pharma 26 Our wide product portfolio 3 Karo Pharma Annual Report 2019 Management review 4 Management review 5 Management review Optimisation of portfolio and Business supply chain Smart model We own and We’re a virtual commercialise company and trusted, high quality, partner for access and key documented and to research and original brands Smart production choices for choices for categories everyday healthcare We occupy a space in the modern
    [Show full text]
  • Annual Report 2015
    Annual Report 2015 3 THIS IS VISTIN PHARMA 3 Highlights and key financial figures 4 Letter from the CEO 6 This is Vistin Pharma 10 Members of the Board 11 The Executive Management 12 Shareholder information 14 FROM THE BOARDROOM 14 Corporate governance 18 Directors' report for 2015 23 Responsibility statement 25 GROUP ACCOUNTS 26 Income statement 27 Comprehensive income statement 28 Balance sheet 29 Changes in equity 30 Cash flow statement 31 Notes to the Group accounts 48 ASA ACCOUNTS 49 Income statement 50 Balance sheet 51 Changes in equity 52 Cash flow statement 53 Notes to the ASA accounts 59 AUDITOR'S REPORT Highlights and key financial figures • The Vistin Pharma group was successfully established in 2015 Key figures from P&L (NOK 000's) 2015 1) . - Acquired the B2B business (metformin and opioids APIs) and tablet production assets Total revenue and income 227 892 Cost of materials 81 646 from Weifa AS for NOK 120 million on 1 June 2015 Other operating expenses 47 282 - Completed a NOK 170 million equity issue EBITDA 27 883 - The shares of Vistin Pharma were listed on Oslo Axess on 10 June 2015 Profit for the year 19 122 • Fifth consecutive year with double digit revenue growth for the metformin Key figures from the balance sheet (NOK 000's) business acquired from Weifa Cash & cash equivalents 61 989 Total assets 259 008 . - Continued strong metformin demand, and supply agreements signed with new customers Borrowings - . - Strong foothold established in the Japanese market Total equity 183 924 . - Agreement signed with a distribution agent for the US market Share data • Stable opioid prices despite continued challenging market Earnings per share – diluted (NOK) 1.12 Number of shares outstanding as of 31.12 17 054 935 .
    [Show full text]
  • Vistin Pharma ASA (A Public Limited Liability Company Organized Under the Laws of Norway)
    Vistin Pharma ASA (A public limited liability company organized under the laws of Norway) Listing of the Shares in Vistin Pharma ASA on Oslo Axess in connection with the offering of 17,054,935 Offer Shares at a Subscription Price of NOK 10 per Offer Share. This prospectus (the “Prospectus”) relates to, and has been issued by Vistin Pharma ASA (the “Company”), solely for use in connection with the offering (the "Offering") and listing on Oslo Axess, a regulated market operated by Oslo Børs ASA (the "Listing") of 17,054,935 new ordinary shares (the "Offer Shares") in the Company, each with a nominal value of NOK 1 and at a subscription price of NOK 10 per Offer Share (the “Subscription Price”). The Offering consists of (i) 15,554,935 new shares at NOK 10 per new share (the “New Shares”) are directed towards the shareholders of Weifa ASA ("Weifa") as of 19 May 2015, registered as such in the Weifa's shareholder register in the Norwegian Central Securities Depository (the "VPS") on 21 May (the "Record Date"), (the “Rights Offering”), who are not resident in a jurisdiction where such offering would be unlawful or would (in jurisdictions other than Norway) require any prospectus filing, registration or similar action (the "Eligible Shareholders") and (ii) 1,500,000 new shares at NOK 10 per new share (the “Employee Offer Shares”) are directed towards the Board of Directors, Executive Management and employees of the Company (the “Employee Offering”). The Employee Offering will be divided into three sub-tranches; (i) 500,000 Employee Offer Shares offered to the Company’s Board of Directors, (ii) 500,000 Employee Offer Shares offered to the Company’s Executive Management, and (iii) 500,000 Employee Offer Shares offered to the Company’s full-time employees as of the date of the transferal of the Acquired Interests.
    [Show full text]
  • Codeine Art. 31
    26 February 2013 EMA/124076/2013 Patient Health Protection Annex I List of the names, pharmaceutical forms, strengths of the medicinal products, routes of administration, marketing authorisation holders in the member states for codeine containing medicinal products used for pain in children Article 31 of Directive 2001/83/EC resulting from pharmacovigilance data Procedure number: EMEA/H/A-31/1342 7 Westferry Circus ● Canary Wharf ● London E14 4HB ● United Kingdom Telephone +44 (0)20 7418 8400 Facsimile +44 (0)20 7418 8416 E -mail [email protected] Website www.ema.europa.eu An agency of the European Union © European Medicines Agency, 2013. Reproduction is authorised provided the source is acknowledged. Member Marketing Product name INN Strength Pharmaceutical Route of State in EEA authorisaton holder form administration Austria Mundipharma GmbH, Codidol retard 60 mg - Dihydrocodeine 60 mg prolonged- oral use Apollogasse 16 - 18 Filmtabletten release tablet 1070 Vienna Austria Austria Mundipharma GmbH, Codidol retard 90 mg - Dihydrocodeine 90 mg prolonged- oral use Apollogasse 16 - 18 Filmtabletten release tablet 1070 Vienna Austria Austria Mundipharma GmbH, Codidol retard 120 mg - Dihydrocodeine 120 mg prolonged- oral use Apollogasse 16 - 18 Filmtabletten release tablet 1070 Vienna Austria Austria G.L. Pharma GmbH, Dehace retard 60 mg - Dihydrocodeine 60 mg prolonged- oral use Schloßplatz 1 Filmtabletten release tablet 8502 Lannach Austria Austria G.L. Pharma GmbH, Dehace retard 90 mg - Dihydrocodeine 90 mg prolonged- oral use Schloßplatz
    [Show full text]
  • Acetaminophen- Clinicalkey
    3/12/2019 Acetaminophen- ClinicalKey DRUG MONOGRAPH Acetaminophen Acephen | Aceta | Actamin | Adult Pain Relief | Anacin Aspirin Free ... Drug Information Provided By Gold Standard Description Acetaminophen (APAP, paracetamol) is a para-aminophenol analgesic and the active metabolite of phenacetin. Due to the toxic effects of phenacetin at therapeutic doses and the availability of acetaminophen, phenacetin is no longer used. Acetaminophen possesses analgesic and antipyretic activity similar to aspirin; however, acetaminophen has no peripheral anti-inflammatory activity or effects on platelet function. Acetaminophen was first used in clinical medicine in the 1890s. It is effective in the relief of both acute and chronic pain and may be preferred over NSAIDs due to fewer hematologic, gastrointestinal, and renal effects. Acetaminophen is the preferred analgesic/antipyretic for patients in whom aspirin is contraindicated and in those with underlying renal disease for episodic, though not chronic, use.23977 In addition, acetaminophen has been recommended by the American Lung Association as the first line treatment for aches and pains associated with the flu, by the American Geriatrics Society for both minor and persistent pain in elderly patients, and by the American College of Rheumatology as first-line therapy for osteoarthritis of the hip or knee.35614 35976 The drug has a history of safe and effective use; however, unintentional or intentional misuse of acetaminophen is the number one cause of acute hepatic failure in the U.S.32202 Acetaminophen was first approved by the FDA in 1950. Intravenous acetaminophen was approved by the FDA in November 2010 for the treatment of pain and fever in adults, adolescents, and children over the age of 2 years.
    [Show full text]
  • Annual Report 2018 in Memoriam Anders Lönner
    Annual Report 2018 In memoriam Anders Lönner KARO PHARMA’S EXECUTIVE icant work for Swedish pharma- CHAIRMAN ANDERS LÖNNER died ceutical research, the Swedish suddenly on 30 November 2018 pharmaceutical industry and at the age of 73. On 23 May 2014, Swedish society generally. he was awarded an honorary As a business leader, Anders’ doctorate in medicine by the approach was highly analyt- Karolinska Institute, with the ical and strategic, qualities citation reading: “through his that were the foundation of entrepreneurship, Anders Lönner his professional decisions. His has been highly significant decisions were also based on to Swedish pharmaceutical In 2014, Anders was awarded an honorary doctorate exceptional judgement and in medicine from the Karolinska Institute, for his sig- research, the Swedish pharma- nificant work for Swedish pharmaceutical research, in-depth experience. As an ceutical industry and Swedish the Swedish pharmaceutical industry and Swedish entrepreneur, he was charac- society generally. society generally.” terized by efficient simplicity, Anders enjoyed a long and successful career in the and he disliked unnecessary bureaucracy. pharmaceutical industry, firstly with Astra AB and Anders was also a master of negotiation, driven by more recently Meda AB. Anders transformed Meda reaching his objective. Rather than get caught up in from a small, local distribution enterprise into a highly the detail, he concentrated on achieving success. successful global specialty pharma company. As By 2018, Anders and the Board of Directors realized Meda’s CEO, Anders created substantial values for the that Karo Pharma’s existing structure was inadequate company’s shareholders, and a great environment for to execute its continued expansion strategy, of creat- the company’s people.
    [Show full text]
  • Aqualis ASA – Annual Report 2014 THIS IS AQUALIS
    AQUALIS ASA ANNUAL REPORT 2014 3 THIS IS AQUALIS 3 Key financial figures 4 Highlights 2014 5 Introducing Aqualis ASA 8 Letter from the Chairman 10 Offshore Oil & Gas 14 Offshore Renewables 16 Members of the Board 17 The Executive Management 20 FROM THE BOARDROOM 20 Corporate governance 24 Directors' report for 2014 29 Responsibility statement 31 GROUP ACCOUNTS 32 Statement of profit and loss 33 Comprehensive income statement 34 Balance sheet 35 Changes in equity 36 Cash flow statement 37 Notes to the Group accounts 57 ASA ACCOUNTS 58 Income statement 59 Balance sheet 60 Cash flow statement 61 Notes to the ASA accounts 69 AUDITOR'S REPORT 2 Aqualis ASA – Annual Report 2014 THIS IS AQUALIS KEY FINANCIAL FIGURES Key figures from P&L (USD 1 000) 2014 2013* Financial calendar 2015 Total operating income 2 241 31 937 EVENT DATE Payroll and payroll related costs 18 563 1 790 Other operating costs 14 575 1 278 First quarter results 28 April Proft/(Loss) after tax -250 -873 Annual General Meeting 22 May Second quarter results 26 August Third quarter results 27 October Key figures from the balance sheet (USD 1 000) Cash & cash equivalents 21 790 838 Borrowings - 5 174 Total assets 51 348 19 901 Ticker symbol Total equity 44 447 12 335 Oslo Børs AQUA Reuters AQUA:OL Share data Bloomberg AQUA:NO Earnings per share (USD) -0.01 Number of shares outstanding as at 31.12 43 190 544 Number of employee share options outstanding at 31.12 750 000 Share price at 31.12 (NOK) 7.55 * Figures for FY 2013 represent historical figures from Weifa ASA’s (former Aqualis ASA) group accounts related to the spin-off of the Aqualis Offshore business.
    [Show full text]
  • Sanofi Finalises Boehringer Deal
    Q&A with Spotlight Time to Weifa’sMonica on win with Børter Bekkhus Genexa diversity page 15 page 8 page 20 Contents Sanofi finalises 13 January 2017 Issue Number 475 COMPANY NEWS Boehringer deal Prestige snaps up Fleet 3 anofi has taken its place as one of the ed to close early in 2017. Boehringer’sacqui- HRA aims to switch4Sworld’stop-three consumer healthcare sition of Merial in Mexico had also been held oral contraceptive companies after completing aswapdeal that up by regulatory delays, the firm noted. Perrigo to focus on 5 has giventhe firm Boehringer Ingelheim’s Over the past fewmonths, Sanofi and Boeh- Belgian turnaround global Consumer Health Carebusiness in ringer had “diligently prepared for the integra- OTCinhaler is hit 6 exchange forits Merial animal health unit. tion of the businesses”, Sanofi pointed out. En- by FDArejection OlivierBrandicourt, Sanofi’schief executive suring “uninterrupted business continuity”, was officer,saidthat combining the French firm’s both companies’ priority to achieve asmooth WBAstrikes deal with Fred’s7 existing Consumer Healthcare business with integration of thetransferred businesses. GENERAL NEWS the German firm’sOTC operation had creat- Commenting on the potential of the newly ed a“strong and innovative”global consumer enlarged Sanofi Consumer Healthcare busi- ASMI against codeine move 9 healthcare company. ness –which will be led by Alan Main (OTC Online OTCmarket10 “Theintegration of Boehringer’shighly-skill- bulletin,7October 2016, page 1) –when the continues to evolve ed consumerhealthcare team and itswell-est- deal wasconfirmed, Sanofi said that it would US issues supplements plan 11 ablished productsallowsSanofi to enhance enhanceits position in severalstrategic cate- its positions in corestrategic categories in a gories, including allergy solutions, cough and MARKETING NEWS promising consumer healthcare environment,” cold care, digestive health, feminine care, and Brandicourt claimed.
    [Show full text]