Ketorolac Versus Other Non-Steroidal Anti-Inflammatory Drugs for the Management of Acute Pain: Comparative Clinical Effectiveness

Total Page:16

File Type:pdf, Size:1020Kb

Ketorolac Versus Other Non-Steroidal Anti-Inflammatory Drugs for the Management of Acute Pain: Comparative Clinical Effectiveness TITLE: Ketorolac versus Other Non-Steroidal Anti-Inflammatory Drugs for the Management of Acute Pain: Comparative Clinical Effectiveness DATE: 16 January 2017 RESEARCH QUESTION What is the comparative clinical effectiveness of ketorolac versus any other non-steroidal anti- inflammatory drug for the management of acute pain? KEY FINDINGS Four randomized controlled trials were identified regarding the comparative clinical effectiveness of ketorolac versus any other non-steroidal anti-inflammatory drug for the management of acute pain. METHODS A limited literature search was conducted on key resources including PubMed, The Cochrane Library, University of York Centre for Reviews and Dissemination (CRD) databases, Canadian and major international health technology agencies, as well as a focused Internet search. To Methodological filters were applied to limit retrieval to health technology assessments, systematic reviews, meta-analyses, randomized controlled trials, non-randomized studies, and guidelines. Where possible, retrieval was limited to the human population. The search was also limited to English language documents published between January 1, 2012 and December 20, 2016. Internet links were provided, where available. The summary of findings was prepared from the abstracts of the relevant information. Please note that data contained in abstracts may not always be an accurate reflection of the data contained within the full article. SELECTION CRITERIA One reviewer screened citations and selected studies based on the inclusion criteria presented in Table 1. Disclaimer: The Rapid Response Service is an information service for those involved in planning and providing health care in Canada. Rapid responses are based on a limited literature search and are not comprehensive, systematic review s. The intent is to provide a list of sources of the best evidence on the topic that the Canadian Agency for Drugs and Technologies in Health (CADTH) could identify using all reasonable efforts within the time allow ed. Rapid responses should be considered along w ith other ty pes of information and health care considerations. The information included in this response is not intended to replace professional medical advice, nor should it be construed as a recommendation for or against the use of a particular health technology. Readers are also cautioned that a lack of good quality evidence does not necessarily mean a lack of effectiveness particularly in the case of new and emerging health technologies, for w hich little information can be found, but w hich may in future prove to be effective. While CADTH has taken care in the preparation of the report to ensure that its contents are accurate, complete and up to date, CADTH does not make any guarantee to that effect. CADTH is not liable for any loss or damages resulting from use of the information in the report. Copyright: This report contains CADTH copyright material and may contain material in w hich a third party ow ns copyright. This report may be used for the purposes of research or private study only. It may not be copied, posted on a w eb site, redistributed by email or stored on an electronic system w ithout the prior w ritten permission of CADTH or applicable copyright ow ner. Links: This report may contain links to other information available on the w ebsites of third parties on the Internet. CADTH does not have control over the content of such sites. Use of third party sites is governed by the ow ners’ ow n terms and conditions. Table 1: Selection Criteria Population Any patient with acute pain Intervention Ketorolac (Toradol) Comparator Non-steroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen, etc.); Excluding aspirin and celecoxib Outcomes Clinical effectiveness, pain management, adverse events Study Designs Health technology assessments, systematic reviews, meta-analyses, randomized controlled trials, non-randomized studies RESULTS Rapid Response reports are organized so that the higher quality evidence is presented first. Therefore, health technology assessment reports, systematic reviews, and meta-analyses are presented first. These are followed by randomized controlled trials, and non-randomized studies. Four randomized controlled trials were identified regarding the comparative clinical effectiveness of ketorolac versus any other non-steroidal anti-inflammatory drug for the management of acute pain. No relevant health technology assessments, systematic reviews, meta-analyses, or non-randomized studies were identified. Additional references of potential interest are provided in the appendix. OVERALL SUMMARY OF FINDINGS Four randomized controlled trials1-4 (RCTs) were identified comparing the effectiveness of ketorolac to other non-steroidal anti-inflammatory drugs. For the management of acute low back pain, one RCT1 determined that sublingual ketorolac was non-inferior to naproxen for the reduction of pain over five days. A higher percentage of patients in the ketorolac group reported improved pain relief within the first 60 minutes after the initial dose. Adverse events included heartburn, nausea, and vomiting.1 Two RCTs2,4 compared intravenous (IV) ketorolac with injectable diclofenac and placebo for the management of post-operative pain. In one RCT,2 acute pain was managed within six hours following orthopedic surgery.2 Mean pain scores were significantly improved in the ketorolac and diclofenac groups when compared with placebo. Significantly better pain scale scores, a lower opioid requirement, and faster onset of pain relief were observed in the diclofenac group as compared to the ketorolac group.2 A second RCT4 compared IV ketorolac with injectable diclofenac and placebo for the management of acute pain following abdominal or pelvic surgery. Both the ketorolac and diclofenac groups reported a significant reduction in pain and requirements for additional morphine when compared with placebo. One serious treatment- related adverse event was reported in the ketorolac group.4 One RCT3 compared the effectiveness of intramuscular ketorolac with diclofenac for the management of pain associated with acute renal colic in the emergency department. A significant difference in pain scores between groups was reported only at 15 minutes following treatment and favored the ketorolac group. There was no significant difference in pain relief between groups at any other time point. No significant differences in adverse events were observed between groups.3 Ketorolac versus Other Non-Steroidal Anti-Inflammatory Drugs for the Management of Acute Pain 2 REFERENCES SUMMARIZED Health Technology Assessments No literature identified. Systematic Reviews and Meta-analyses No literature identified. Randomized Controlled Trials 1. Plapler PG, Scheinberg MA, Ecclissato Cda C, Bocchi de Oliveira MF, Amazonas RB. Double-blind, randomized, double-dummy clinical trial comparing the efficacy of ketorolac trometamol and naproxen for acute low back pain. Drug Des Devel Ther [Internet]. 2016 [cited 2017 Jan 11];10:1987-93. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918732 PubMed: PM27382251 2. Daniels S, Melson T, Hamilton DA, Lang E, Carr DB. Analgesic efficacy and safety of a novel injectable formulation of diclofenac compared with intravenous ketorolac and placebo after orthopedic surgery: a multicenter, randomized, double-blinded, multiple- dose trial. Clin J Pain. 2013 Aug;29(8):655-63. PubMed: PM23328337 3. Kolasani B, Juturu J. Intramuscular ketorolac versus diclofenac in acute renal colic: A comparative study of efficacy and safety. Indian Journal of Basic & Applied Medical Research [Internet]. 2013 Sep [cited 2017 Jan 11];8(2): 923-931. Available from: http://ijbamr.com/pdf/923-931.pdf.pdf 4. Gan TJ, Daniels SE, Singla N, Hamilton DA, Carr DB. A novel injectable formulation of diclofenac compared with intravenous ketorolac or placebo for acute moderate-to-severe pain after abdominal or pelvic surgery: a multicenter, double-blind, randomized, multiple- dose study. Anesth Analg. 2012 Nov;115(5):1212-20. PubMed: PM22886837 Non-Randomized Studies No literature identified. PREPARED BY: Canadian Agency for Drugs and Technologies in Health Tel: 1-866-898-8439 www.cadth.ca Ketorolac versus Other Non-Steroidal Anti-Inflammatory Drugs for the Management of Acute Pain 3 APPENDIX – FURTHER INFORMATION: Previous CADTH Reports 5. Canadian Agency for Drugs and Technologies in Health. Ketorolac for pain management: a review of the clinical evidence [Internet]. Ottawa (ON): CADTH; 2014 Jun 30. (CADTH rapid response reports: Summary with critical appraisal). [cited 2017 Jan 11]. Available from: https://www.cadth.ca/ketorolac-pain-management-review-clinical-evidence Systematic Reviews – Comparison to Other NSAIDs Not Specified in Abstract 6. Marmura MJ, Silberstein SD, Schwedt TJ. The acute treatment of migraine in adults: the american headache society evidence assessment of migraine pharmacotherapies. Headache. 2015 Jan;55(1):3-20. PubMed: PM25600718 7. Orr SL, Aube M, Becker WJ, Davenport WJ, Dilli E, Dodick D, et al. Canadian Headache Society systematic review and recommendations on the treatment of migraine pain in emergency settings. Cephalalgia. 2015 Mar;35(3):271-84. PubMed: PM24875925 8. Taggart E, Doran S, Kokotillo A, Campbell S, Villa-Roel C, Rowe BH. Ketorolac in the treatment of acute migraine: a systematic review. Headache. 2013 Feb;53(2):277-87. PubMed: PM23298250 Randomized Controlled Trials – Different Doses of Ketorolac 9. Motov S, Yasavolian M, Likourezos A, Pushkar
Recommended publications
  • Efficacy and Safety of Celecoxib
    ORIGINAL PAPER Nagoya J. Med. Sci. 77. 81 ~ 93, 2015 EFFICACY AND SAFETY OF CELECOXIB COMPARED WITH PLACEBO AND ETODOLAC FOR ACUTE POSTOPERATIVE PAIN: A MULTICENTER, DOUBLE-BLIND, RANDOMIZED, PARALLEL-GROUP, CONTROLLED TRIAL NAOKI ISHIGURO1, MD, PhD; AKIO HANAOKA2, MS; TOSHIYUKI OKADA2, MS; and MASANORI ITO3, PhD 1Department of Orthopedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan 2Clinical Development 1, Astellas Pharma Inc., Tokyo, Japan 3Global Data Science, Astellas Pharma Global Development Inc., Northbrook, IL, US ABSTRACT Celecoxib is a nonsteroidal anti-inflammatory drug (selective cyclooxygenase-2 inhibitor) that is widely used. The efficacy and safety of celecoxib for treatment of acute postoperative pain were evaluated in Japanese patients. The objective was to assess whether celecoxib showed superiority over placebo treatment and non-inferiority versus etodolac (another selective cyclooxygenase-2 inhibitor) that has been widely used for the management of acute pain. A multicenter, double-blind, randomized, parallel-group, controlled study was performed, in which 616 patients with postoperative pain received celecoxib, etodolac, or placebo. Their impressions of study drug efficacy (overall assessment) and pain intensity were evaluated. Based on each patient’s overall assessment of pain, the efficacy rate was 63.7% in the placebo group, 76.2% in the celecoxib group, and 68.0% in the etodolac group, with these results demonstrating superiority of celecoxib to placebo and noninferiority versus etodolac. The efficacy rate was significantly higher in the celecoxib group than in the etodolac group. There were no adverse events specific to celecoxib, and the safety of celecoxib was similar to that of placebo. Celecoxib was superior to etodolac for controlling acute postoperative pain.
    [Show full text]
  • New Restrictions on Celecoxib (Celebrex) Use and the Withdrawal of Valdecoxib (Bextra)
    Early release, published at www.cmaj.ca on April 15, 2005. Subject to revision. HEALTH AND DRUG ALERTS P RACTICE New restrictions on celecoxib (Celebrex) use and the withdrawal of valdecoxib (Bextra) Early release, published at www.cmaj.ca on Apr. 15, 2005. Subject to revision. Reason for posting: Coxibs, v. 0.5%; risk ratio 3.7, 95% CI the class of NSAIDs that selec- 1.0–13.5).2 Amid concerns about Table 1: The degree of inhibition of COX-2 relative tively inhibit cyclooxygenase 2 reports of severe cutaneous reac- to COX-1 for various NSAIDs (COX-2), were designed to re- tions (Stevens–Johnson syn- NSAID type COX-2 selectivity* duce joint pain and inflamma- drome, erythema multiforme, tion without causing the gastric toxic epidermal necrolysis) COX-2 selective inhibitors epithelial adverse effects typical among patients taking valde- Rofecoxib 80 of nonselective NSAIDs. Rofe- coxib,5 the drug was removed Etodolac 23 coxib (Vioxx) was withdrawn from the market. Meloxicam 11 from the market in September Celecoxib 9 2004 over concerns about car- What to do: COX-2 inhibitors Nonselective NSAIDs diovascular adverse effects, and appear to increase the risk of car- Diclofenac 4 key safety trials involving cele- diovascular adverse events in a Sulindac 3 coxib (Celebrex)1 and valdecoxib dose-related fashion, and all pa- Piroxicam 2 (Bextra)2 have recently been tients should be informed of this. Ibuprofen 0.4 published. Health Canada now Calculating the patient’s baseline Naproxen 0.3 recommends new restrictions on risk of cardiovascular disease Indomethacin 0.2 celecoxib use, and valdecoxib (e.g., with Framingham risk cal- Ketorolac 0.003 has been taken off the market.3 culators) may be wise, and cele- Note: COX = cyclooxygenase.
    [Show full text]
  • Nsaids: Dare to Compare 1997
    NSAIDs TheRxFiles DARE TO COMPARE Produced by the Community Drug Utilization Program, a Saskatoon District Health/St. Paul's Hospital program July 1997 funded by Saskatchewan Health. For more information check v our website www.sdh.sk.ca/RxFiles or, contact Loren Regier C/O Pharmacy Department, Saskatoon City Hospital, 701 Queen St. Saskatoon, SK S7K 0M7, Ph (306)655-8506, Fax (306)655-8804; Email [email protected] We have come a long way from the days of willow Highlights bark. Today salicylates and non-steroidal anti- • All NSAIDs have similar efficacy and side inflammatory drugs (NSAIDs) comprise one of the effect profiles largest and most commonly prescribed groups of • In low risk patients, Ibuprofen and naproxen drugs worldwide.1 In Saskatchewan, over 20 may be first choice agents because they are different agents are available, accounting for more effective, well tolerated and inexpensive than 300,000 prescriptions and over $7 million in • Acetaminophen is the recommended first line sales each year (Saskatchewan Health-Drug Plan agent for osteoarthritis data 1996). Despite the wide selection, NSAIDs • are more alike than different. Although they do Misoprostol is the only approved agent for differ in chemical structure, pharmacokinetics, and prophylaxis of NSAID-induced ulcers and is to some degree pharmacodynamics, they share recommended in high risk patients if NSAIDS similar mechanisms of action, efficacy, and adverse cannot be avoided. effects. week or more to become established. For this EFFICACY reason, an adequate trial of 1-2 weeks should be NSAIDs work by inhibiting cyclooxygenase (COX) allowed before increasing the dose or changing to and subsequent prostaglandin synthesis as well as another NSAID.
    [Show full text]
  • Food and Drug Administration, HHS § 201.323
    Food and Drug Administration, HHS § 201.323 liver damage or gastrointestinal bleed- calcium, choline salicylate, magnesium ing). OTC drug products containing in- salicylate, or sodium salicylate] or ternal analgesic/antipyretic active in- other pain relievers/fever reducers. [Ac- gredients may cause similar adverse ef- etaminophen and (insert one nonste- fects. FDA concludes that the labeling roidal anti-inflammatory analgesic/ of OTC drug products containing inter- antipyretic ingredient—including, but nal analgesic/antipyretic active ingre- not limited to aspirin, carbaspirin cal- dients should advise consumers with a cium, choline salicylate, magnesium history of heavy alcohol use to consult salicylate, or sodium salicylate] may a physician. Accordingly, any OTC cause liver damage and stomach bleed- drug product, labeled for adult use, ing.’’ containing any internal analgesic/anti- (b) Requirements to supplement ap- pyretic active ingredients (including, proved application. Holders of approved but not limited to, acetaminophen, as- applications for OTC drug products pirin, carbaspirin calcium, choline sa- that contain internal analgesic/anti- licylate, ibuprofen, ketoprofen, magne- pyretic active ingredients that are sub- sium salicylate, naproxen sodium, and ject to the requirements of paragraph sodium salicylate) alone or in combina- (a) of this section must submit supple- tion shall bear an alcohol warning ments under § 314.70(c) of this chapter statement in its labeling as follows: to include the required warning in the (1) Acetaminophen. ‘‘Alcohol Warn- product’s labeling. Such labeling may ing’’ [heading in boldface type]: ‘‘If you be put into use without advance ap- consume 3 or more alcoholic drinks proval of FDA provided it includes the every day, ask your doctor whether exact information included in para- you should take acetaminophen or graph (a) of this section.
    [Show full text]
  • New Zealand Data Sheet 1
    New Zealand Data Sheet 1. PRODUCT NAME NAXEN® 250 mg tablets 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each NAXEN 250 mg tablet contains 250 mg of Naproxen For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM NAXEN 250 mg tablets are yellow, biconvex, round tablet of 11 mm diameter with one face engraved NX250 and having a bisecting score. The score line is only to facilitate breaking for ease of swallowing and not to divide into equal doses. 4. CLINICAL PARTICULARS 4.1. Therapeutic indications NAXEN is indicated in adults for the relief of symptoms associated with rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, tendonitis and bursitis, acute gout and primary dysmenorrhoea. NAXEN is indicated in children for juvenile arthritis. 4.2. Dose and method of administration After assessing the risk/benefit ratio in each individual patient, the lowest effective dose for the shortest possible duration should be used (see Section 4.4). During long-term administration the dose of naproxen may be adjusted up or down depending on the clinical response of the patient. A lower daily dose may suffice for long-term administration. In patients who tolerate lower doses well, the dose may be increased to 1000 mg per day when a higher level of anti-inflammatory/analgesic 1 | P a g e activity is required. When treating patients with naproxen 1000 mg/day, the physician should observe sufficient increased clinical benefit to offset the potential increased risk. Dose Adults For rheumatoid arthritis, osteoarthritis and ankylosing spondylitis Initial therapy: The usual dose is 500-1000 mg per day taken in two doses at 12 hour intervals.
    [Show full text]
  • Colonoscopy Instructions
    Colonoscopy Checklist Five days before your colonoscopy: Stop any medications that thin the blood (see list below) Discuss the discontinuation of these medications with your primary care physician to ensure that it is safe to stop them Three days before your colonoscopy: Stop eating high fiber foods including nuts, corn, popcorn, raw fruits, vegetables, and bran Stop fiber supplements The day before your colonoscopy: Have a normal breakfast If your colonoscopy is scheduled before noon the following day, do not have any lunch If your colonoscopy is scheduled after noon, have a light lunch Have clear liquids for the rest of the day (see below) Start prep as instructed by your physician Do not have anything to eat or drink after midnight The day of your colonoscopy: Take your blood pressure medications with a sip of water Make sure you bring your driver’s license or photo ID and leave valuables and jewelry at home Clear Liquid Diet Water Any kind of soft drink (ginger ale, cola, tonic, etc) Gatorade Apple Juice Orange Juice without pulp Lemonade Tea/Coffee (without milk) Dietary supplements (Ensure, Boost, Enlive, etc) Clear broth (vegetable, chicken, or beef) Jell‐O (stay away from red, blue, or purple colors) Ice pops without milk or fruit bits Honey or sugar NO DAIRY PRODUCTS Medications to stop prior to colonoscopy Below is a list of many medications (but not all) that fall into these categories. It is important to remember that there are hundreds of over‐the‐counter medications that contain NSAIDs or aspirin, so it is important to carefully read the label of any medication that you are taking (prescription or over‐the‐counter).
    [Show full text]
  • (Ketorolac Tromethamine Tablets) Rx Only WARNING TORADOL
    TORADOL ORAL (ketorolac tromethamine tablets) Rx only WARNING TORADOLORAL (ketorolac tromethamine), a nonsteroidal anti-inflammatory drug (NSAID), is indicated for the short-term (up to 5 days in adults), management of moderately severe acute pain that requires analgesia at the opioid level and only as continuation treatment following IV or IM dosing of ketorolac tromethamine, if necessary. The total combined duration of use of TORADOLORAL and ketorolac tromethamine should not exceed 5 days. TORADOLORAL is not indicated for use in pediatric patients and it is NOT indicated for minor or chronic painful conditions. Increasing the dose of TORADOLORAL beyond a daily maximum of 40 mg in adults will not provide better efficacy but will increase the risk of developing serious adverse events. GASTROINTESTINAL RISK Ketorolac tromethamine, including TORADOL can cause peptic ulcers, gastrointestinal bleeding and/or perforation of the stomach or intestines, which can be fatal. These events can occur at any time during use and without warning symptoms. Therefore, TORADOL is CONTRAINDICATED in patients with active peptic ulcer disease, in patients with recent gastrointestinal bleeding or perforation, and in patients with a history of peptic ulcer disease or gastrointestinal bleeding. Elderly patients are at greater risk for serious gastrointestinal events (see WARNINGS). CARDIOVASCULAR RISK NSAIDs may cause an increased risk of serious cardiovascular thrombotic events, myocardial infarction, and stroke, which can be fatal. This risk may increase with duration of use. Patients with cardiovascular disease or risk factors for cardiovascular disease may be at greater risk (see WARNINGS and CLINICAL STUDIES). TORADOL is CONTRAINDICATED for the treatment of peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery (see WARNINGS).
    [Show full text]
  • Medication Guide for Non-Steroidal Anti-Inflammatory Drugs (Nsaids)
    Medication Guide for Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) (See the end of this Medication Guide for a list of prescription NSAID medicines.) What is the most important information I should know about medicines called Non-Steroidal Anti- Inflammatory Drugs (NSAIDs)? NSAID medicines may increase the chance of a heart attack or stroke that can lead to death. This chance increases: • with longer use of NSAID medicines • in people who have heart disease NSAID medicines should never be used right before or after a heart surgery called a “coronary artery bypass graft (CABG).” NSAID medicines can cause ulcers and bleeding in the stomach and intestines at any time during treatment. Ulcers and bleeding: can happen without warning symptoms may cause death The chance of a person getting an ulcer or bleeding increases with: ▪ taking medicines called "corticosteroids” and “anticoagulants” ▪ longer use ▪ smoking ▪ drinking alcohol ▪ older age ▪ having poor health NSAID medicines should only be used: • exactly as prescribed • at the lowest dose possible for your treatment • for the shortest time needed What are Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)? NSAID medicines are used to treat pain and redness, swelling, and heat (inflammation) from medical conditions such as: different types of arthritis menstrual cramps and other types of short-term pain Who should not take a Non-Steroidal Anti-Inflammatory Drug (NSAID)? Do not take an NSAID medicine: • if you had an asthma attack, hives, or other allergic reaction with aspirin or any other NSAID medicine • for pain right before or after heart bypass surgery Tell your healthcare provider: • about all of your medical conditions.
    [Show full text]
  • Celecoxib but Not Rofecoxib Inhibits the Growth of Transformed Cells in Vitro
    Vol. 10, 267–271, January 1, 2004 Clinical Cancer Research 267 Celecoxib But Not Rofecoxib Inhibits the Growth of Transformed Cells in Vitro Diana Kazanov,1 Hadas Dvory-Sobol,1,3 Conclusions: Celecoxib may prove to be a very efficient Marjorie Pick,2 Eliezer Liberman,1,3 component in the prevention and treatment of gastrointes- Ludmila Strier,1 Efrat Choen-Noyman,1,3 tinal tumors because it inhibits the growth of cancerous cells without affecting the growth of normal cells. Varda Deutsch,2,3 Talya Kunik,1 and Nadir Arber1,3 Departments of 1Cancer Prevention and 2Hematology, Tel Aviv INTRODUCTION Medical Center, and 3Sackler Faculty of Medicine, Tel Aviv Colorectal cancer (CRC), with an estimated lifetime risk of University, Tel Aviv, Israel 5–6%, is a major health concern in the Western world (1, 2). The goal of achieving effective cancer prevention is driven by ABSTRACT the prediction that cancer will become the leading cause of death (surpassing heart disease) during this decade, with an estimated Purpose: Nonsteroidal anti-inflammatory drugs reduce 1,000,000 new cases and Ͼ500,000 deaths/year, worldwide the risk of colorectal cancer. The cyclooxygenase (COX) (1–3). Despite continuing advances in diagnosis and therapy, pathway of arachidonic acid metabolism is an important long-term survival has not improved significantly over the last target for nonsteroidal anti-inflammatory drugs. Increased four decades. Nearly 50% of all CRC patients will eventually expression of COX-2 was recently shown to be an important die of their disease (1, 2). step in the multistep process of colorectal cancer carcino- The association between nonsteroidal anti-inflammatory genesis.
    [Show full text]
  • Clinical Outcomes of Aspirin Interaction with Other Non-Steroidal Anti- Inflammatory Drugs: a Systematic Review
    J Pharm Pharm Sci (www.cspsCanada.org) 21, 48s – 73s, 2018 Clinical Outcomes of Aspirin Interaction with Other Non-Steroidal Anti- Inflammatory Drugs: A Systematic Review Zuhair Alqahtani and Fakhreddin Jamali Faculty of Pharmacy and Pharmaceutical Science, University of Alberta, Edmonton, Alberta, Canada. Received, March 16, 2018; Revised, March 30, 2018; Accepted, April 25, 2018; Published, April 27, 2018. ABSTRACT - Purpose: Concomitant use of some non-Aspirin nonsteroidal anti-inflammatory drugs (NANSAIDs) reduces the extent of platelet aggregation of Aspirin (acetylsalicylic acid). This is while many observational studies and clinical trials suggest that Aspirin reduces cardiovascular (CV) risk attributed to the use of NANSAIDs. Thus, the therapeutic outcome of the interaction needs to be assessed. Methods: We searched various databases up to October 2017 for molecular interaction studies between the drugs and long-term clinical outcomes based on randomized clinical trials and epidemiological observations that reported the effect estimates of CV risks (OR, RR or HR; 95% CI) of the interacting drugs alone or in combinations. Comparisons were made between outcomes after Aspirin alone, NANSAIDs alone and Aspirin with naproxen, ibuprofen, celecoxib, meloxicam, diclofenac or rofecoxib. Results: In total, 32 eligible studies (20 molecular interactions studies and 12 observational trials) were found. Conflicting in vitro/in vivo/ex vivo platelet aggregation data were found for ibuprofen, naproxen and celecoxib. Nevertheless, for naproxen, the interaction at the aggregation level did not amount to a loss of cardioprotective effects of Aspirin. Similarly, for ibuprofen, the results overwhelmingly suggest no negative clinical CV outcomes following the combination therapy. Meloxicam and rofecoxib neither interacted with Aspirin at the level of platelet aggregation nor altered clinical outcomes.
    [Show full text]
  • Central Nervous System Toxicity of Mefenamic Acid
    Central Nervous System toxicity of mefenamic acid overdose compared to other NSAIDs: an analysis of cases reported to the United Kingdom National Poisons Information Service. Running header: CNS toxicity of mefenamic acid A Kamour1, S Crichton2, G Cooper3, DJ Lupton4, M Eddleston4,5, JA Vale6, JP Thompson 3, SHL Thomas1,7 1National Poisons Information Service, Newcastle Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Wolfson Unit, Claremont Place, Newcastle upon Tyne, NE2 4HH. 2Department of Primary Care and Public Health, King's College London, Capital House, London, SE1 3QD 3National Poisons Information Service, Cardiff Unit, University Hospital Llandough, Penlan Road, Penarth, Vale of Glamorgan CF64 2XX. 4National Poisons Information Service, Edinburgh Unit, Royal Infirmary of Edinburgh, 51 Little France Crescent, Old Dalkeith Road, Edinburgh EH16 4SA. 5Pharmacology, Toxicology and Therapeutics, University/BHF Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK. 6National Poisons Information Service, Birmingham Unit, City Hospital, Dudley Road, Birmingham B18 7QH. 7Medical Toxicology Centre, Institute of Cellular Medicine, Wolfson Building, Newcastle University, Newcastle NE2 4HH. Address for correspondence: Dr Ashraf Kamour, Acute Medical Unit, North Manchester General Hospital Delaunays Road, Crumpsall, Manchester, M8 5RB, UK. Tel: +44 (0)161 918 4673 This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process which may lead to differences between this version and the Version of Record. Please cite this article as doi: 10.1111/bcp.13169 This article is protected by copyright. All rights reserved. Fax: +44 (0)161 604 5323 Email: [email protected] Keywords: Mefenamic acid, non-steroidal anti-inflammatory drug, overdose, poisoning, CNS toxicity, convulsions.
    [Show full text]
  • CELECOXIB Information That Patients Need to Know About Their Medication
    CELECOXIB Information That Patients Need to Know About Their Medication Kelsey L. Fletcher, BS Medical Student Wake Forest School of Medicine Winston-Salem, North Carolina Mary Lynn McPherson, PharmD, BCPS, CPE Professor and Vice Chair Department of Pharmacy Practice and Science University of Maryland, School of Pharmacy Baltimore, Maryland pain, cough or respiratory infections. Celecoxib may cause What is celecoxib? or worsen high blood pressure. Celecoxib (pronounced se le KOKS ib) is a nonsteroidal While taking celecoxib you should avoid drinking alco- anti-inflammatory drug (NSAID) that has been prescribed hol because it may increase your risk of stomach bleeding. by your doctor to relieve or prevent your pain. Celecoxib You should also avoid using celecoxib in combination with is available as an oral tablet. Another name you may see on other NSAIDs such as ibuprofen (Motrin, Advil), naproxen the prescription label is Celebrex. (Aleve), diclofenac (Arthrotec, Cambia, Cataflam, Voltaren) and others. Ask your doctor or pharmacist before taking What is it used for? other cold, allergy or pain medications, as they may contain Celecoxib is used for the management of acute pain in adults, medications similar to celecoxib. pain associated with menstrual cramps, and to treat the pain Celecoxib should not be used if you have a history of of arthritis including: allergic reaction to aspirin, sulfa drugs or other NSAIDs. If • Osteoarthritis taken for long periods of time, celecoxib can cause increased • Rheumatoid arthritis risk of cardiovascular events such as stroke and heart attack. • Juvenile rheumatoid arthritis in children over two Celecoxib may also have serious effects on the stomach and • Ankylosing spondylosis intestines, including bleeding and ulcers.
    [Show full text]