Catalyst Rx 2010 National Preferred Formulary
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(12) Patent Application Publication (10) Pub. No.: US 2011/0244057 A1 Ehrenberg (43) Pub
US 2011024.4057A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2011/0244057 A1 Ehrenberg (43) Pub. Date: Oct. 6, 2011 (54) COMBINATION THERAPIES WITH Related U.S. Application Data TOPIRAMATE FOR SEIZURES, RESTLESS LEGS SYNDROME, AND OTHER (60) Provisional application No. 61/100,232, filed on Sep. NEUROLOGICAL CONDITIONS 25, 2008. Publication Classification (51) Int. Cl. (76) Inventor: Bruce L. Ehrenberg, New York, A633/26 (2006.01) NY (US) A63L/35 (2006.01) A633/06 (2006.01) A6IP 25/00 (2006.01) (21) Appl. No.: 13/120,933 A6IP 25/28 (2006.01) A6IP 25/08 (2006.01) (22) PCT Filed: Sep. 25, 2009 (52) U.S. Cl. .......... 424/648: 514/454; 424/682; 424/646 (57) ABSTRACT (86). PCT No.: PCT/US2009/058495 The invention provides compositions and methods of treating various conditions, including neurological conditions, with S371 (c)(1), pharmaceutical compositions including a sulfamate (e.g., (2), (4) Date: Jun. 9, 2011 topiramate) and magnesium. US 2011/024.4057 A1 Oct. 6, 2011 COMBINATION THERAPES WITH TOPIRAMATE FOR SEIZURES, RESTLESS LEGS SYNDROME, AND OTHER II NEUROLOGICAL CONDITIONS CROSS-REFERENCE TO RELATED APPLICATIONS 0001. This application claims the benefit of the priority date of U.S. Application No. 61/100,232, filed Sep. 25, 2008. For the purpose of any U.S. patent that may issue from the 0005 wherein RandR, are the same or different and are U.S. national phase correlate of the present application, the hydrogen, lower alkyl or are alkyl and are joined to form a content of the priority document is hereby incorporated by cyclopentyl or cyclohexyl ring, and (b) magnesium. -
Staged Anticonvulsant Screening for Chronic Epilepsy
Staged anticonvulsant screening for chronic epilepsy The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Berdichevsky, Yevgeny, Yero Saponjian, Kyung#Il Park, Bonnie Roach, Wendy Pouliot, Kimberly Lu, Waldemar Swiercz, F. Edward Dudek, and Kevin J. Staley. 2016. “Staged anticonvulsant screening for chronic epilepsy.” Annals of Clinical and Translational Neurology 3 (12): 908-923. doi:10.1002/acn3.364. http://dx.doi.org/10.1002/ acn3.364. Published Version doi:10.1002/acn3.364 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:30371039 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA RESEARCH ARTICLE Staged anticonvulsant screening for chronic epilepsy Yevgeny Berdichevsky1,a, Yero Saponjian2,3,a, Kyung-Il Park4,a, Bonnie Roach5, Wendy Pouliot5, Kimberly Lu6, Waldemar Swiercz2,3, F. Edward Dudek5 & Kevin J. Staley2,3 1Department of Electrical and Computer Engineering and Bioengineering Program, Lehigh University, Bethlehem, Pennsylvania 18015 2Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts 02129 3Harvard Medical School, Boston, Massachusetts 02129 4Department of Neurology, Seoul National University Hospital Healthcare System Gangnam Center, Seoul, South Korea 06236 5Department of Neurosurgery, University of Utah School of Medicine, Salt Lake City, Utah 84108 6Boston University School of Medicine, Boston, Massachusetts 02119 Correspondence Abstract Kevin J. Staley, Department of Neurology, Massachusetts General Hospital, Boston, MA Objective: Current anticonvulsant screening programs are based on seizures 02129. -
Treatment of Myoclonus with Pheneturide
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.41.7.598 on 1 July 1978. Downloaded from Journal ofNeurology, Neurosurgery, andPsychiatry, 1978, 41, 598-602 Treatment of myoclonus with pheneturide C. D. WARD From the Royal Hospital, Sheffield S U M M A R Y Twenty-one patients with various forms of myoclonus are presented. Phena- cemide was given to five patients with considerable benefit to three, but with serious toxic effects in two. Another acetylurea derivative, pheneturide, was given to 19 patients and was well tolerated. Myoclonus was completely or substantially controlled in 12 patients. The term "myoclonus" may be applied to very between 1965 and 1976. They had displayed myo- abrupt involuntary movements which are neur- clonic jerks and had been treated with phena- onally determined, asynergic, and arrhythmic. An cemide or pheneturide. Of these patients, 16 were assortment of involuntary movements share these seen personally for review and three responded to characteristics but differ in their relationship to a questionnaire. Records of outpatient follow-up movement, relaxation, posture, or sensory stimuli, were available for one patient who had died and Protected by copyright. and in their anatomical disposition (Gasaut, 1968); for one who could not be traced. All had given a they may involve parts of muscles, whole muscles, history of repeated, instantaneous involuntary or, more usually, muscle groups. Such movements, movements and had reported at least one of the collectively termed myoclonus, are seen in a wide following: sudden jerks of the arms causing ob- variety of pathological conditions (Halliday, 1967) jects to fly out of the hands; sudden interruption and may often be associated with epilepsy. -
Pharmaceuticals As Environmental Contaminants
PharmaceuticalsPharmaceuticals asas EnvironmentalEnvironmental Contaminants:Contaminants: anan OverviewOverview ofof thethe ScienceScience Christian G. Daughton, Ph.D. Chief, Environmental Chemistry Branch Environmental Sciences Division National Exposure Research Laboratory Office of Research and Development Environmental Protection Agency Las Vegas, Nevada 89119 [email protected] Office of Research and Development National Exposure Research Laboratory, Environmental Sciences Division, Las Vegas, Nevada Why and how do drugs contaminate the environment? What might it all mean? How do we prevent it? Office of Research and Development National Exposure Research Laboratory, Environmental Sciences Division, Las Vegas, Nevada This talk presents only a cursory overview of some of the many science issues surrounding the topic of pharmaceuticals as environmental contaminants Office of Research and Development National Exposure Research Laboratory, Environmental Sciences Division, Las Vegas, Nevada A Clarification We sometimes loosely (but incorrectly) refer to drugs, medicines, medications, or pharmaceuticals as being the substances that contaminant the environment. The actual environmental contaminants, however, are the active pharmaceutical ingredients – APIs. These terms are all often used interchangeably Office of Research and Development National Exposure Research Laboratory, Environmental Sciences Division, Las Vegas, Nevada Office of Research and Development Available: http://www.epa.gov/nerlesd1/chemistry/pharma/image/drawing.pdfNational -
BMJ Open Is Committed to Open Peer Review. As Part of This Commitment We Make the Peer Review History of Every Article We Publish Publicly Available
BMJ Open is committed to open peer review. As part of this commitment we make the peer review history of every article we publish publicly available. When an article is published we post the peer reviewers’ comments and the authors’ responses online. We also post the versions of the paper that were used during peer review. These are the versions that the peer review comments apply to. The versions of the paper that follow are the versions that were submitted during the peer review process. They are not the versions of record or the final published versions. They should not be cited or distributed as the published version of this manuscript. BMJ Open is an open access journal and the full, final, typeset and author-corrected version of record of the manuscript is available on our site with no access controls, subscription charges or pay-per-view fees (http://bmjopen.bmj.com). If you have any questions on BMJ Open’s open peer review process please email [email protected] BMJ Open Pediatric drug utilization in the Western Pacific region: Australia, Japan, South Korea, Hong Kong and Taiwan Journal: BMJ Open ManuscriptFor ID peerbmjopen-2019-032426 review only Article Type: Research Date Submitted by the 27-Jun-2019 Author: Complete List of Authors: Brauer, Ruth; University College London, Research Department of Practice and Policy, School of Pharmacy Wong, Ian; University College London, Research Department of Practice and Policy, School of Pharmacy; University of Hong Kong, Centre for Safe Medication Practice and Research, Department -
Therapeutic Class Overview Anticonvulsants
Therapeutic Class Overview Anticonvulsants Therapeutic Class Overview/Summary: The anticonvulsants are Food and Drug Administration (FDA)-approved for the prevention and/or treatment of various seizure disorders either as monotherapy or adjunctive therapy. Some anticonvulsants are also FDA-approved for the prevention of migraines, and management of bipolar disorders, fibromyalgia, neuropathic pain and other non-seizure related conditions. The specific FDA-approved indications for each of these agents are outlined in Table 1.1-44 Seizure disorders are classified into four major categories: partial seizures (seizures beginning locally), generalized seizures (bilaterally symmetrical and without local onset), unilateral seizures (seizures that are predominantly unilateral) and unclassified epileptic seizures (seizures that are unclassifiable because of incomplete data). Partial seizures are subdivided into those with elementary symptomatology, those with complex symptomatology, and those that are secondarily generalized. Partial seizures with elementary symptomatology include those with motor symptoms (e.g., Jacksonian seizures) or with autonomic symptoms. Partial seizures with complex symptomatology are also known as temporal lobe or psychomotor seizures. Generalized seizures include tonic-clonic (grand mal) seizures, absence (petit mal) seizures, myoclonic seizures and akinetic seizures. Two or more seizures that occur sequentially without full recovery of consciousness between the seizures or seizures that last more than 30 minutes are known as status epilepticus.45 Pharmacologic management of epilepsy should be individualized, and focused on controlling seizures, avoiding treatment-related adverse events and maintaining or restoring quality of life.46 Prior to 1990, six major antiepileptic drugs were available for the treatment of various forms of epilepsy, including carbamazepine, ethosuximide, phenobarbital, phenytoin, primidone and valproic acid. -
Showed Atrophy and Cystic Changes in the Left Hemisphere with Compensatory Dilatation of the Lateral Ventricle
increased. MRI showed atrophy and cystic changes in the left hemisphere with compensatory dilatation of the lateral ventricle. Thalidomide (300 mg/day) was added to a midazolam iv drip, and partial seizure control was sustained. For the past 3 years, her seizures have been less intense and less frequent and have not interfered with everyday activities. Treatment includes thalidomide 5 mg/kg, valproate 30 mg/kg, clonazepam and piracetam. Apart from occasional leukopenia, no other adverse effects are reported. (Maijanovic BD, Stojanov LM, Zdravkovic DS et al. Rasmusen syndrome and long-term response to thalidomide. Pediatr Neurol Aug 2003;29:151-156). (Respond: Dr Maijanovic, Department of Neurology, Pediatric Clinic of Mother and Child Health Care Institute, Belgrade, Yugoslavia). COMMENT. Thalidomide may be considered as an alternative treatment for refractory and incapacitating seizures in Rasmussen syndrome, when more conventional therapies have failed. One previous report found thalidomide effective in a 7-year-old male with Rasmussen syndrome whose seizures were associated with high levels of CSF tumor necrosis factor a. (Ravenscroft A et al. Brain Dev 1998;20:398). The antiepileptic effect may be related to inhibition of the tumor necrosis factor and boosting of the immune response. Apart from the high teratogenicity, a sensory neuropathy is the major adverse complication of thalidomide therapy. LEVETIRACETAM IN LANDAU-KLEFFNER SYNDROME A 5-year-old girl with seizures and progressive language deterioration and a diagnosis of Landau-Kleffner syndrome was benefited by treatment with levetiracetam at Johns Hopkins Hospital, Baltimore, MD. Video-EEG monitoring showed continuous 2- to 3-Hz spike-wave discharges, maximal left, during sleep. -
********.*****::****A::*************-A***I '************** * Reproductions Supplied by EDRS Are the Best That Can Be Made from the Original Document
DOCUMENT RESUME ED 372 587 EC 303 220 AUTHOR Lassner, Lee M. TITLE Epilepsy in the Classroom: Guidance for Educators. PUB DATE Nov 93 NOTE 31p.; Paper presented at the Annpal Meeting of the Mid South Educational Research Association (New Orleans, LA, November 10-12, 1993). PUB TYPE Guides Non-Classroom Use (055) Speeches/Conference Papers (150) EDRS PRICE MF01/PCO2 Plus Postage. DESCRIPTORS Academic Achievement; Counselor Role; Definitions; Disability Identification; Drug Therapy; *Educational Needs; Elementary Secondary Education; *Epilepsy; Mainstreaming; Peer Relationship; *Seizures; Special Health Problems; *Symptoms (Individual Disorders); Teacher Role ABSTRACT This paper for educators, school psychologists, and counselors attempts to provide guidance for meeting the needs of students with epilepsy. Stressed throughout the paper are ways to provide for the child's special needs while fostering his/her self esteem and full participation in classroom activities. The paper addresses the following topics: (1) what epilepsy is;(2) types of epilepsy;(3) recognizing epileptic seizures;(4) identification, evaluation, and correct placement; (5) consultation; (6) counseling; (7) coordination of programs;(8) research;(9) specific knowledge educators, counselors, and children should have;. (10) medicines for epilepsy and their side effects;(11) administration of antiepileptic drugs by school officials;(12) seizure management; (13) epilepsy and academic achievement; (14) epilepsy and athletics; and (15) the future. Contains 22 references. (BIB) -
Pharmacotherapy for Stimulant Use Disorders: a Systematic Review
4 D epartment of Veterans Affairs Health Services Research & Development Service Evidence-based Synthesis Program Pharmacotherapy for Stimulant Use Disorders: A Systematic Review August 2018 Prepared for: Investigators: Department of Veterans Affairs Principal Investigator: Veterans Health Administration Brian Chan, MD, MPH Quality Enhancement Research Initiative Co-Investigators: Health Services Research & Development Service Karli Kondo, PhD, MA Washington, DC 20420 Chelsea Ayers, BA Prepared by: Michele Freeman, MPH Jessica Montgomery, MPH Evidence-based Synthesis Program (ESP) Robin Paynter, MLIS Portland VA Health Care System Devan Kansagara, MD, MCR Portland, OR Devan Kansagara, MD, MCR, Director 4 Pharmacotherapy for Stimulant Use Disorders Evidence-based Synthesis Program PREFACE The VA Evidence-based Synthesis Program (ESP) was established in 2007 to provide timely and accurate syntheses of targeted healthcare topics of particular importance to clinicians, managers, and policymakers as they work to improve the health and healthcare of Veterans. QUERI provides funding for 4 ESP Centers, and each Center has an active University affiliation. Center Directors are recognized leaders in the field of evidence synthesis with close ties to the AHRQ Evidence-based Practice Centers. The ESP is governed by a Steering Committee comprised of participants from VHA Policy, Program, and Operations Offices, VISN leadership, field-based investigators, and others as designated appropriate by QUERI/HSR&D. The ESP Centers generate evidence syntheses on important clinical practice topics. These reports help: · Develop clinical policies informed by evidence; · Implement effective services to improve patient outcomes and to support VA clinical practice guidelines and performance measures; and · Set the direction for future research to address gaps in clinical knowledge. -
SUPPLEMENT Etable 1
SUPPLEMENT eTable 1. List of medications used for exclusions and prescription drug history variables Anticonvulsants (past use Medications used for prescription drug history variables evaluated as an exclusion criterion) Antidepressants Anticholinergics Carbamazepine Bupropion Aclidinium Clobazam Atropine Clonazepam Other antidepressants: Cyclopentolate Clorazepate Amitriptyline Glycopyrrolate Diazepam Amoxapine Homatropine Divalproex Butriptyline Ipratropium Ethosuximide Citalopram Methscopolamine Ethotoin Clomipramine Scopolamine Ezogabine Desipramine Tiotropium Felbamate Desvenlafaxine Tropicamide Fosphenytoin Dibenzepin Gabapentin Dotheipin Lacosamide Doxepin Lamotrigine Duloxetine Levetiracetam Escitalopram Lorazepam Fluoxetine Mephenytoin Fluvoxamine Mephobarbital Imipramine Metharbital Iprindole Methsuximide Isocarboxazid Oxcarbazepine Levomilnacipran Paramethadione Lofepramine Phenacemide Maprotiline Phenobarbital Melitracen Phensuximide Mianserin Phenytoin Milnacipran Pregabalin Mirtazapine Primidone Nefazodone Rufinamide Nortriptyline Tiagabine Opipramol Topiramate Paroxetine Trimethadione Phenelzine Valproate Sodium Protriptyline Valproic Acid Sertraline Vigabatrin Tranylcypromine Zonisamide Trazodone Trimipramine Tryptophan Venlafaxine Vilazodone 1 eTable 2. Diagnostic codes used for medical history variables Medical condition Diagnostic codes (ICD-9)a Stroke 431.xx, 433.xx, 434.xx, 436.xx Other cerebrovascular 430.xx, 432.xx, 435.xx, 437.xx, 438.xx disease Brain injury 850.xx-854.xx, 907.0x Hypoxemia 799.02 Infection 001.xx-039.xx -
Nervous System Drug Poster
Nervous System Drugs Created by the Njardarson Group (The University of Arizona): Edon Vitaku, Elizabeth A. Ilardi, Daniel J. Mack, Monica A. Fallon, Erik B. Gerlach, Miyant’e Y. Newton, Angela N. Yazzie, Jack Siqueiros, Jón T. Njarðarson Cocaine Aspirin Caffeine Procaine Benzocaine Metharbital Oxycodone Disulfiram Morphine Ergotamine Hydromorphone Codeine Pemoline Amphetamine Thiopental Methadone Methadone Biperiden Thiopental D.H.E. Trimethadione Urecholine Cafergot ( Cocaine ) ( Aspirin ) ( Caffeine ) ( Procaine ) ( Benzocaine ) ( Metharbital ) ( Oxycodone ) ( Disulfiram ) ( Morphine ) ( Ergotamine ) ( Hydromorphone ) ( Codeine ) ( Pemoline ) ( Amphetamine ) ( Thiopental ) ( Methadone ) ( Methadone ) ( Biperiden ) ( Thiopental ) ( Dihydroergotamine ) ( Trimethadione ) ( Bethanechol ) ( Ergotamine & Caffeine ) ANESTHETIC ANALGESIC PSYCHOANALEPTIC ANESTHETIC ANESTHETIC ANTIEPILEPTIC ANALGESIC MISC. NERVOUS ANALGESIC ANALGESIC ANALGESIC ANALGESIC PSYCHOANALEPTIC PSYCHOANALEPTIC ANESTHETIC ANALGESIC MISC. NERVOUS ANTI-PARKINSON PSYCHOLEPTIC ANALGESIC ANTIEPILEPTIC MISC. NERVOUS ANALGESIC Approved 1880 Approved 1899 Approved 1900 Approved 1900 Approved 1902 Approved 1905 Approved 1916 Approved 1920 Approved 1920 Approved 1921 Approved 1926 Approved 1930 Approved 1930 Approved 1933 Approved 1934 Approved 1937 Approved 1937 Approved 1940 Approved 1940 Approved 1946 Approved 1947 Approved 1948 Approved 1948 Lidocaine Artane Anileridine Chlor-Trimeton Clonidine Ethchlorvynol Imipramine Morphine Percodan Paramethadione Secobarbital Apomorphine -
WO 2010/015029 Al
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date 11 February 2010 (11.02.2010) WO 2010/015029 Al (51) International Patent Classification: (74) Agent: FISHER ADAMS KELLY; Level 29 Comalco A61K 31/19 (2006.01) A61P 25/28 (2006.01) Place, 12 Creek Street, Brisbane, Queensland 4000 (AU). A61K 31/445 (2006.01) A61K 31/35 (2006.01) (81) Designated States (unless otherwise indicated, for every A61P 25/26 (2006.01) A61P 25/18 (2006.01) kind of national protection available): AE, AG, AL, AM, A61K 31/137 (2006.01) A61K 31/4192 (2006.01) AO, AT, AU, AZ, BA, BB, BG, BH, BR, BW, BY, BZ, A61P 25/08 (2006.01) A61P 25/24 (2006.01) CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, (21) International Application Number: DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, PCT/AU2009/001000 HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, (22) International Filing Date: ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, 6 August 2009 (06.08.2009) NO, NZ, OM, PE, PG, PH, PL, PT, RO, RS, RU, SC, SD, (25) Filing Language: English SE, SG, SK, SL, SM, ST, SV, SY, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (26) Publication Language: English (84) Designated States (unless otherwise indicated, for every (30) Priority Data: kind of regional protection available): ARIPO (BW, GH, 2008904016 6 August 2008 (06.08.2008) AU GM, KE, LS, MW, MZ, NA, SD, SL, SZ, TZ, UG, ZM, 2008904021 6 August 2008 (06.08.2008) AU ZW), Eurasian (AM, AZ, BY, KG, KZ, MD, RU, TJ, (71) Applicant (for all designated States except US): GOS- TM), European (AT, BE, BG, CH, CY, CZ, DE, DK, EE, FORTH CENTRE (HOLDINGS) PTY LTD [AU/AU]; ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, Level 1, 66 Duporth Avenue, Maroochydore, queensland MC, MK, MT, NL, NO, PL, PT, RO, SE, SI, SK, SM, 4558 (AU).