Applied Numerics in System Biology

Total Page:16

File Type:pdf, Size:1020Kb

Applied Numerics in System Biology Applied numerics in system biology Max von Kleist Vitaly Belik Vikram Sunkara About me 2004 MS Physics, Biophysics, Moscow Lomonosov University 2000-2001 HU Berlin 2008 Dr. rer. nat. Georg-August-Universität Göttingen 2010-2012 MIT, Cambridge, MA 2004-2013 MPI for Dynamics and Selforganisation, Göttingen 2014-2016 TU Berlin since 2016 Professor (Juniorprofessor) FU Berlin AG System Modeling, Institut für veterinary Epidemiology and Biostatistics [email protected] Research focus Spreading processes on networks (epidemiology, opinion formation) Human and animal mobility Combining biological and metadata Data science (sensor data for health applications) Host-parasite-environment interactions, hormone dynamics Epidemics V Belik, T Geisel, D Brockmann Physical Review X 1 (1), 011001 Underlying network (A) (B) (C) V Belik, T Geisel, D Brockmann Physical Review X 1 (1), 011001 Human mobility 4 II II II I IIIII I II IIIIV I II III IV 40% 6 30% 3/5 4/83 4/5408 4/10 Survey Phone 20% (ID) Model p 10% 0% 1 2345 6 7 8 9 10 11 12 13 14 15 16 17 Motif ID FIG. 3. Possible daily mobility patterns are limited, since up to 90% of the identified daily mobility networks can be described with only 17CM different Schneider, motifs. The probability V Belik,p(ID) T Couronné, to find one of the Z 17 Smoreda, motifs in the surveys MC (cyan González - Paris, blue - Chicago), the phone data (orange - Paris), and the model (light green - Paris, dark green - Chicago) is presented. The motifs are grouped according toJournal their size separated of The by Royal dashed lines Society and for each Interface group the fraction 10 (84), of observed 20130246 and feasible motifs Nf are shown. Most of the motifs can also be classified with four rules: I) The motif of size N consists of a tour with only one stop and another tour with N 2stops.II)ThemotifofsizeN consists of only a single tour with N stops. III) The motif of size N consists of two tours with− one stop and another tour with N 3stops.IV)ThemotifofsizeN consists of a tour with two stops and another tour with N 3 stops. Despite the fact that− the number of workers is significantly different in both cities, the rank and the probability to− find a specific motif exhibit similar behavior. than one. In fact, this is observed for motifs created ac- While the time spent for working and staying at home is cording to rule II) and III). relatively flat distributed with some characteristic dura- In general, motifs may not be unique, if a person can re- tions of 3.5h, 8.6h, and 14h, respectively, the probability peat a tour several times within a day. However, the rep- of an activity at another place decreases with its dura- etition of tours is uncommon, thus an edge corresponds tion. The staying time distribution has no characteristic to exactly one trip. In the survey data, the observed mo- duration, suggesting that the location change follows an tifs without multiple trips are su⇥cient to reproduce over underlying ’bursty’ behavior - the location changes are 95% of the travel behavior correctly and we observe that not distributed evenly over time, but in groups inter- tours T (x)withx>1 are performed only once during a spersed with periods of inactivity. To support this obser- day (for details see SI). vation, we study the time between two similar activities, These observations imply that each person has a char- shown in Fig. 5B. While the time based on home and acteristic daily motif although the visited locations can work are governed by the daily routines, the time between change. Thus a user has a personal number of preferred other locations shows in fact that in the trip selection re- places on a daily basis, which are more likely visited in a lated to flexible activities ’bursts’ exist. This temporal specific sequence given by its motif. inter-event dynamics has been reported in specific human activities such as web browsing, printing patterns, email, and phone communication [31, 39–42], but it has not been II. PERTURBATION-BASED MODEL incorporated in models of human mobility. Inspired by these observations, we developed a perturbation-based model, to reproduce not only the observed daily motifs, It is surprising that nearly the entire population can be but also their frequency of occurrence. described with a few unique daily motifs. To understand In the following the model for a non-working (NW) agent this observation, we study the time spent at certain lo- is explained and the additional, minor features for work- cations as well as the time between the starting time of ing (W) agents are described in the SI. Accounting for an activity and the next activity of the same kind. the difference of the home and other locations, the model From both surveys the frequency of staying at a place for assumes a fixed activity at home and any number of flex- a particular time period is extracted for three groups of ible activities elsewhere (shopping, recreation, etc.). The activities, home, work, and other, as shown in Fig. 5A. Animal trade network Animation by T Selhorst H Lentz et al., Trade communities and their spatial patterns in the German pork production network, Preventive veterinary medicine, 98, 176 (2011) Swine trade network 4000 nodes with edges occurring more than 50 times ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms10331 Metabolism, Pancreatic kidney Liver Liver Myocardial Arteriosclerosis Vascular Arterial Heart inborn diseases diseases cirrhosis cirrhosis, ischemia diseases occlusive diseases errors biliary diseases Hydrochlorothiazide Allopurinol Torasemide Enoxaparin Bivalirudin Niacin Papaverine Bentiromide Losartan Colchicine Epoprostenol Pentoxifylline Tolvaptan Tirofiban Eptifibatide Streptokinase Biotin Enalapril Furosemide Ethacrynic Irbesartan Spironolactone acid Perindopril Isosorbide Dofetilide mononitrate Flecainide Mexiletine Sulfinpyrazone Lidocaine Vitamin A Coronary Verapamil Cardiomyopathy, Malabsorption Liraglutide Varicose Procainamide disease dilated syndromes veins Sodium Isosorbide Amiodarone Disopyramide Glimepiride Dinitrate Chlorpropamide Tolbutamide tetradecyl Moricizine sulfate Sotalol Insulin aspart Diabetes Amrinone mellitus, Sitagliptin Fenofibrate Propafenone Arrhythmias, Propranolol Diabetes Miglitol Insulin lispro type 2 Atorvastatin Lovastatin Quinidine cardiac mellitus, Ibutilide Acebutolol type 1 Nateglinide Tolazamide Digoxin Diabetes Coronary DronedaroneDiltiazem Gliclazide Pioglitazone Cardiovascular mellitus artery Isoproterenol Gastroenteritis Hyperinsulinism Glyburide Rosiglitazone Simvastatin diseases disease Diazoxide Loperamide Metformin Acarbose Pravastatin Lung Probucol Orlistat Mycobacterium Bone diseases infections diseases Zoledronate Joint Bacterial Insulin Rifabutin Colorectal diseases Budesonide infections resistance Inflammatory neoplasms CalcitriolPamidronate bowel Tetracycline Ciprofloxacin Cilastatin Levofloxacin diseases Intestinal Ketoprofen Floxuridine Cholecalciferol neoplasms Keratosis Naproxen Leflunomide Indomethacin Ibuprofen Salicyclic acid Neuroendocrine Erlotinib Bone Chloroquine Thyroid Diclofenac tumors Octreotide diseases, Auranofin Colitis Mycophenolic metabolic diseases Etodolac Tazarotene Mesalazine Sunitinib Calcidiol Liothyronine Triamcinolone Gastrointestinal Psoriasis Acitretin neoplasms Sulfasalazine Pilocarpine Adenocarcinoma Sulindac Celecoxib Hydroxyurea Endocrine Head and neck system Arthritis, Hypopigmentation Arthritis rheumatoid neoplasms diseases Crohn's Leukaemia,Teniposide Cyclosporine Monobenzone disease lymphoid Arsenic Hydrocortisone Hydroxychloroquine Leukaemia, Progesterone trioxide Colitis, Daunorubicin myeloid, Gefitinib ulcerative Leukaemia acute Imatinib Theophylline Dexamethasone Nicotine Cromoglicic Tiotropium acid Olsalazine Lupus Sarcoma Oxtriphylline Mercaptopurine Dacarbazine Aminophylline Salbutamol erythematosus, Alitretinoin Skin Balsalazide systemic Cytarabine Arformoterol Methotrexate Docetaxel diseases Vincristine Nedocromil Asthma Calcipotriol Haematological Doxorubicin Zafirlukast Azathioprine diseases Isoetharine Lymphoma Atropine Pimecrolimus Bleomycin Ephedrine Prednisolone Fluticasone Dyphylline Neoplasms propionate Montelukast Fluocinonide Ketotifen Prednisone Zileuton Cladribine Epirubicin Pseudoephedrine Vinblastine Eye Capecitabine diseases Collagen Rheumatic Macular diseases diseases Kidney Breast degeneration Hypersensitivity neoplasms neoplasms Letrozole Chlorpheniramine Mitoxantrone Lomustine Autoimmune Tamoxifen Megestrol Multiple Fludarabine Pegaptanib Diphenhydramine diseases sclerosis Carmustine Medroxyprogesterone Promethazine Plerixafor Fluoxymesterone Vinorelbine Baclofen Estradiol HistamineCyproheptadine Methylprednisolone Spinal Bicalutamide Conjugated Dexrazoxane Tizanidine estrogens Phosphate Fingolimod cord Flutamide Methyltestosterone Parkinsonian Dantrolene Aminoglutethimide diseases Chlorotrianisene disorders Trihexyphenidyl Quetiapine Diethylstilbestrol Citalopram Motor Ropinirole Risperidone Amyotrophic Prostatic neuron Leuprolide neoplasms Blood disease lateral Goserelin coagulation Levodopa Biperiden sclerosis Estramustine Aneamia, Finasteride disorders Amantadine Dementia hemolytic Phytonadione Zhong at al. Mol. Sys. Bio. Apomorphine Clonazepam Carbidopa Tranexamic Riluzole Lamotrigine 12: 865 (2016) Pyridoxine Topiramate Primidone acid Donepezil # of disease Benzatropine Parkinson Rivastigmine Vitamin E Diazepam Disease genes disease Pregabalin 20 ... 500 Rasagiline Epilepsy Selegiline Alzheimer Acetazolamide Gabapentin Drug Folic acid Aneamia # of targets
Recommended publications
  • Vitiligo Treatment
    ISSN 2320-5407 International Journal of Advanced Research (2014) Journal homepage: http://www.journalijar.com INTERNATIONAL JOURNAL OF ADVANCED RESEARCH Depigmentation Therapy for Vitiligo: Results from a National Survey Dissertation submitted to Libyan International Medical University In partial fulfillment of the requirements For the award of the degree of Bachelor of Pharmacy BY Makpula Abdelaziz Tarhuni Aisha Ali Derbash Under The Guidance of Dr. Salma Bukhatwa 1 ISSN 2320-5407 International Journal of Advanced Research (2014) Declaration This is to certify that research work embodied in this thesis entitled "Depigmentation therapy of vitiligo: Results from a national survey" has been carried out by us under supervision of Dr. Salma Bukhatwa. Makpula Abdelaziz Tarhuni ................................................... Aisha Ali Derbash ...................................................... 2 ISSN 2320-5407 International Journal of Advanced Research (2014) Abstract Vitiligo is a chronicpigmentarydisorderthat causes the loss of skin color in blotches. Vitiligo happens because of destruction of melanocytes. Classification of vitiligo according to distribution of the lesions is of practical importance usually for assessing the prognosis of the disease. Repigmentation therapyfor vitiligo includes corticosteroids, topical and oral antioxidants, topical calcineurin inhibitors, phototherapy and laser therapy. Depigmentation therapy can be beneficial as alternative therapy for extensive vitiligo patients. Depigmentation therapyof vitiligo
    [Show full text]
  • Drug Name Plate Number Well Location % Inhibition, Screen Axitinib 1 1 20 Gefitinib (ZD1839) 1 2 70 Sorafenib Tosylate 1 3 21 Cr
    Drug Name Plate Number Well Location % Inhibition, Screen Axitinib 1 1 20 Gefitinib (ZD1839) 1 2 70 Sorafenib Tosylate 1 3 21 Crizotinib (PF-02341066) 1 4 55 Docetaxel 1 5 98 Anastrozole 1 6 25 Cladribine 1 7 23 Methotrexate 1 8 -187 Letrozole 1 9 65 Entecavir Hydrate 1 10 48 Roxadustat (FG-4592) 1 11 19 Imatinib Mesylate (STI571) 1 12 0 Sunitinib Malate 1 13 34 Vismodegib (GDC-0449) 1 14 64 Paclitaxel 1 15 89 Aprepitant 1 16 94 Decitabine 1 17 -79 Bendamustine HCl 1 18 19 Temozolomide 1 19 -111 Nepafenac 1 20 24 Nintedanib (BIBF 1120) 1 21 -43 Lapatinib (GW-572016) Ditosylate 1 22 88 Temsirolimus (CCI-779, NSC 683864) 1 23 96 Belinostat (PXD101) 1 24 46 Capecitabine 1 25 19 Bicalutamide 1 26 83 Dutasteride 1 27 68 Epirubicin HCl 1 28 -59 Tamoxifen 1 29 30 Rufinamide 1 30 96 Afatinib (BIBW2992) 1 31 -54 Lenalidomide (CC-5013) 1 32 19 Vorinostat (SAHA, MK0683) 1 33 38 Rucaparib (AG-014699,PF-01367338) phosphate1 34 14 Lenvatinib (E7080) 1 35 80 Fulvestrant 1 36 76 Melatonin 1 37 15 Etoposide 1 38 -69 Vincristine sulfate 1 39 61 Posaconazole 1 40 97 Bortezomib (PS-341) 1 41 71 Panobinostat (LBH589) 1 42 41 Entinostat (MS-275) 1 43 26 Cabozantinib (XL184, BMS-907351) 1 44 79 Valproic acid sodium salt (Sodium valproate) 1 45 7 Raltitrexed 1 46 39 Bisoprolol fumarate 1 47 -23 Raloxifene HCl 1 48 97 Agomelatine 1 49 35 Prasugrel 1 50 -24 Bosutinib (SKI-606) 1 51 85 Nilotinib (AMN-107) 1 52 99 Enzastaurin (LY317615) 1 53 -12 Everolimus (RAD001) 1 54 94 Regorafenib (BAY 73-4506) 1 55 24 Thalidomide 1 56 40 Tivozanib (AV-951) 1 57 86 Fludarabine
    [Show full text]
  • Patent Application Publication ( 10 ) Pub . No . : US 2019 / 0192440 A1
    US 20190192440A1 (19 ) United States (12 ) Patent Application Publication ( 10) Pub . No. : US 2019 /0192440 A1 LI (43 ) Pub . Date : Jun . 27 , 2019 ( 54 ) ORAL DRUG DOSAGE FORM COMPRISING Publication Classification DRUG IN THE FORM OF NANOPARTICLES (51 ) Int . CI. A61K 9 / 20 (2006 .01 ) ( 71 ) Applicant: Triastek , Inc. , Nanjing ( CN ) A61K 9 /00 ( 2006 . 01) A61K 31/ 192 ( 2006 .01 ) (72 ) Inventor : Xiaoling LI , Dublin , CA (US ) A61K 9 / 24 ( 2006 .01 ) ( 52 ) U . S . CI. ( 21 ) Appl. No. : 16 /289 ,499 CPC . .. .. A61K 9 /2031 (2013 . 01 ) ; A61K 9 /0065 ( 22 ) Filed : Feb . 28 , 2019 (2013 .01 ) ; A61K 9 / 209 ( 2013 .01 ) ; A61K 9 /2027 ( 2013 .01 ) ; A61K 31/ 192 ( 2013. 01 ) ; Related U . S . Application Data A61K 9 /2072 ( 2013 .01 ) (63 ) Continuation of application No. 16 /028 ,305 , filed on Jul. 5 , 2018 , now Pat . No . 10 , 258 ,575 , which is a (57 ) ABSTRACT continuation of application No . 15 / 173 ,596 , filed on The present disclosure provides a stable solid pharmaceuti Jun . 3 , 2016 . cal dosage form for oral administration . The dosage form (60 ) Provisional application No . 62 /313 ,092 , filed on Mar. includes a substrate that forms at least one compartment and 24 , 2016 , provisional application No . 62 / 296 , 087 , a drug content loaded into the compartment. The dosage filed on Feb . 17 , 2016 , provisional application No . form is so designed that the active pharmaceutical ingredient 62 / 170, 645 , filed on Jun . 3 , 2015 . of the drug content is released in a controlled manner. Patent Application Publication Jun . 27 , 2019 Sheet 1 of 20 US 2019 /0192440 A1 FIG .
    [Show full text]
  • 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
    [Show full text]
  • Vitiligo AHM
    Vitiligo AHM Clinical indication Any one of the following established methods for the treatment of Vitiligo is considered medically necessary : o Excimer laser (e.g., XTRAC, PhotoMedex, Radnor, PA; EX-308, Ra Medical Systems, Inc., Carlsbad, CA) o Narrow-band ultraviolet B (UVB) o Topical and oral psoralen photochemotherapy (PUVA) Note: Continued PUVA or narrow-band UVB therapy is not medically necessary unless there is significant follicular pigmentation after 6 months of therapy (8 to 10 treatments per month) o Topical and systemic corticosteroids Indications considered Not Medically Necessary Treatments for vitiligo are considered cosmetic if they do not affect the underlying condition and do not result in improved protection against skin cancer; specifically micropigmentation (tattooing) and depigmentation (with monobenzylether of hydroquinone/monobenzone) are considered cosmetic. The following treatments for the condition vitiligo are considered not medically necessary as there is a lack of evidence regarding the safety and effectiveness have not been established o Home phototherapy o Melanocyte transplantation/cultured and non-cultured cellular melanocyte keratinocyte transfer for the treatment of vitiligo o Vitamin D analogs (e.g., calcitriol and paricalcitol) o Tumor necrosis factor-alpha agents (e.g., adalimumab, etanercept, and infliximab) o Alpha-melanocyte stimulating hormone (e.g., afamelanotide) o Chimeric monoclonal antibody to CD20 (e.g., rituximab) o Autologous mini-punching grafting, blister roof grafting (suction epidermal blister grafting) and split thickness skin grafting AC-AEVITI082014 Page 1 of 5 Copyright 2016 No part of this document may be reproduced without permission ActiveHealth Management Medical Management Guidelines References: 1. Grimes PE. Diseases of hypopigmentation. In: Principles and Practice of Dermatology.
    [Show full text]
  • Mortar & Pestle
    Nebraska January/February 2020 | Volume 83, Number 1 MORTAR & PESTLE Official Publication of theNebraska Pharmacists Association Pam Miller 2020 NPA President Member Spotlight - Sabrina Beck | Pg 6 For NPA Members Vitiligo & Treatment Options | Pg 8 Rx and The Law | Pg 17 Baqsimi - New Delivery for Glucagon | Pg 18 Financial Forum | Pg 26 Trelegy - New Triple Therapy | Pg 28 Nebraska MORTAR & PESTLE CPE Programs npharm.org/npacpeprograms Fraud, Waste, and Abuse USP Chapter <800> Handling Hazardous Drugs in 1.0 hour Knowledge-based CPE Activity Healthcare Setting: Considerations for STERILE Products $10 NPA Member | $20 NonMember and Compounding 1.0 hour Knowledge-based CPE Activity How to Engage Your Senators: You Can Make $25 NPA Member | $50 NonMember a Difference 1.0 hour Knowledge-based CPE Activity USP Chapter <800> Handling Hazardous Drugs in $0 NPA Member | $25 NonMember Healthcare Setting: Considerations for Non-Sterile Products and Compounding Nicotine Cessation Counseling: A Guide for Pharmacists 1.0 hour Knowledge-based CPE Activity 2.0 hours Knowledge-based CPE Activity $25 NPA Member | $50 NonMember $25 NPA Member | $50 NonMember Risky Business: Assessment of Risk on Hazardous Drugs 1.0 hour Knowledge-based CPE Activity $25 NPA Member | $50 NonMember NPA Staff Joni Cover, JD Marcia Mueting, PharmD Diane Webb Sarah Hunter Chief Executive Officer VP, Professional Affairs Finance & Marketing Project Coordinator Pharmacy Technician Second class postage paid at Lincoln, Board of Directors Publisher Nebraska, and at additional mailing offices. Tyler Garrelts The Nebraska Mortar & Pestle (M&P) (ISSN President, Pam Miller Postmaster: send address changes to 0028-1891) is owned and published by Immediate Past President, Nebraska Mortar & Pestle, 6221 S 58th St, the Nebraska Pharmacists Association to Suite A, Lincoln, NE 68516-3687 or email Ally Dering-Anderson Students provide continuing pharmacy education, [email protected].
    [Show full text]
  • FDA Listing of Established Pharmacologic Class Text Phrases January 2021
    FDA Listing of Established Pharmacologic Class Text Phrases January 2021 FDA EPC Text Phrase PLR regulations require that the following statement is included in the Highlights Indications and Usage heading if a drug is a member of an EPC [see 21 CFR 201.57(a)(6)]: “(Drug) is a (FDA EPC Text Phrase) indicated for Active Moiety Name [indication(s)].” For each listed active moiety, the associated FDA EPC text phrase is included in this document. For more information about how FDA determines the EPC Text Phrase, see the 2009 "Determining EPC for Use in the Highlights" guidance and 2013 "Determining EPC for Use in the Highlights" MAPP 7400.13.
    [Show full text]
  • Important Note:All Human Products Must Be Of
    * Important Note:All human products must be of human recombinant origin wherever these are available in the market *For oral solution it is preferable:Syrup then Suspension and then Elixir MOH CODE ITEM NAME Qty 1 CARDIOVASCULAR SYSTEM 1A Positive inotropic drugs 1Aa Digtalis glycoside 02-01-00001 digoxin tab 62.5 mcg 800,000 02-01-00002 digitoxin tab 100 mcg 800,000 02-01-00003 digoxin tab 125 mcg 800,000 02-01-00004 digoxin tab 250 mcg 30,415,200 02-01-00005 digoxin PG elixir 50mcg /ml 800,000 02-01-00006 digoxin inj 250 mcg/ml, (2ml amp) 800,000 1Ab PHOSPHODIESTERASE INHIBITORS 02-01-00007 Enoximone inj 5mg/ml (20ml amp) 800,000 1B DIURETICS 02-01-00008 amiloride Hcl 5mg + hydrochlorthiazide 50mg tab 50,000,000 02-01-00009 bumetanide tab 1 mg 1,094,000 02-01-00010 chlorthalidone tab 50mg 3,264,000 02-01-00011 ethacrynic acid as sod.salt inj powder for 800,000 reconstitution 50mg vial 02-01-00012 frusemide inj 20mg/2ml amp 5,780,400 02-01-00013 frusemide I.V. infusion inj 10mg/ml, (25ml amp) 800,000 02-01-00014 frusemide tab 40mg 25,000,000 02-01-00015 frusemide scored tab 500mg 800,000 02-01-00016 frusemide oral solution pead liquid 1mg/1ml 800,000 02-01-00017 frusemide oral solution 4mg/ml 800,000 02-01-00018 frusemide oral solution 8mg/ml 800,000 02-01-00019 hydrochlorothiazide tab 25mg 1,084,000 02-01-00020 hydrochlorothiazide tab 50mg 1,396,000 02-01-00021 indapamide tab 2.5mg 800,000 02-01-00022 Indapamide s/r coated tab 1.5mg 800,000 02-01-00023 spironolactone tab 25mg 5,568,400 02-01-00024 spironolactone tab 100mg 5,147,200
    [Show full text]
  • 2018 Formulary Drug List
    2018 Formulary Drug List For Small Groups and Large Groups GlobalHealth, Inc. 701 NE 10th Street, Suite 300 Oklahoma City, OK 73104-5403 MGDF18 Lists Updated 11/2017 www.GlobalHealth.com/commercial HELPFUL NUMBERS Plan Issuer: Medication Prior Authorizations: GlobalHealth, Inc. [email protected] PO Box 2393 918.878.7361 Oklahoma City, OK 73101-2393 Mail Claims to: GlobalHealth Customer Care, Language Magellan Rx Management, LLC Assistance, and Disease Management: PO Box 85042 [email protected] Richmond, VA 23261-5042 405.280.2964 (local) 1.877.280.2964 (toll-free) Mail Order Pharmacy: 711 (TTY) Magellan Rx Management, LLC Monday – Friday, 9 a.m. – 5 p.m. Central 1.800.424.1789 (toll-free) www.GlobalHealth.com/commercial 711 (TTY) P.O. Box 620968 Behavioral Health and Substance Use: Orlando, FL 32862 [email protected] 405.280.2964 (local) 24/7 Nurse Help Line: 1.877.280.2964 (toll-free) Information Line 711 (TTY) 1.877.280.2993 (toll-free) Monday – Friday, 9 a.m. – 5 p.m. Central www.GlobalHealth.com/commercial GlobalHealth Compliance Officer: 1.877.280.5852 (toll-free) Pharmacy Benefits Manager: 405.280.5852 Magellan Rx Management, LLC [email protected] Customer Service 1.800.424.1789 (toll-free) GlobalHealth Privacy Officer: 711 (TTY) 405.280.5524 [email protected] i IMPORTANT INFORMATION This formulary applies to Members who enrolled through an employer in any of the following Plans: Platinum Plan 1 without Dental Gold Plan 1 with Dental Gold Plan 1 without Dental Standard Plan Member Materials Your comprehensive Member handbook has three booklets.
    [Show full text]
  • Ibm Micromedex® Carenotes Titles by Category
    IBM MICROMEDEX® CARENOTES TITLES BY CATEGORY DECEMBER 2019 © Copyright IBM Corporation 2019 All company and product names mentioned are used for identification purposes only and may be trademarks of their respective owners. Table of Contents IBM Micromedex® CareNotes Titles by Category Allergy and Immunology ..................................................................................................................2 Ambulatory.......................................................................................................................................3 Bioterrorism ...................................................................................................................................18 Cardiology......................................................................................................................................18 Critical Care ...................................................................................................................................20 Dental Health .................................................................................................................................22 Dermatology ..................................................................................................................................23 Dietetics .........................................................................................................................................24 Endocrinology & Metabolic Disease ..............................................................................................26
    [Show full text]
  • Clinuvel Price Target: AUD 31.70 Reuters: CUV.AX Bloomberg: CUV:AU the Light Protection Enabler
    30 January 2018 Rating: Buy Risk: High Price: AUD 8.65 Clinuvel Price target: AUD 31.70 Reuters: CUV.AX Bloomberg: CUV:AU The light protection enabler We’re initiating coverage of Australian Clinuvel with a WKN/ISIN: A0JEGY/AU000000CUV3 buy rating and a price target of AUD 31.70 per share, Indices: All Ordinaries Index (XAO) since we believe investors are not fully factoring in Transparency level: n/a potential opportunities to Clinuvel’s long-term growth in Weighted average number of share: 47.7 mn the global skin protection market. The orphan disease Market cap: AUD 412.9 mn drug company is dramatically expanding top-line growth Daily trading volume: ~40,000 shares in the near-term as we expect the company to expand its Next AGM: n/a global footprint in EPP. Apart from these significant growth opportunities, that even a rare disease like EPP AUD mn (31/12) 2016 2017 2018e 2019e offers, we expect even more in the years to come, since Revenues 6.4 17.0 46.3 133.4 (1) Clinuvel is expected to launch its vitiligo product in EBITDA -3.1 7.2 22.7 72.0 2021e, representing a substantial larger market than the EBIT -3.2 7.1 22.5 71.6 rare disease EPP, (2) the launch of a topical product EBT -3.2 7.1 22.8 72.0 should make room for the mass market of non- EAT -3.2 7.1 22.8 72.0 prescription skin care solutions, and (3) Clinuvel could also offer a treatment for various Central Nervous % of revenues.
    [Show full text]
  • Pharmaceutical Cream Compositions Comprising Oxymetazoline to Treat Rosacea
    (19) TZZ¥___ __T (11) EP 3 181 121 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 21.06.2017 Bulletin 2017/25 A61K 9/10 (2006.01) A61K 31/4174 (2006.01) A61K 47/10 (2017.01) A61K 47/14 (2017.01) (2006.01) (21) Application number: 16196317.8 A61K 9/00 (22) Date of filing: 01.12.2011 (84) Designated Contracting States: • POWALA, Christopher AL AT BE BG CH CY CZ DE DK EE ES FI FR GB Radnor GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO Pennsylvania 19087 (US) PL PT RO RS SE SI SK SM TR • RIOS, Luis Pembroke Pines (30) Priority: 03.12.2010 US 419693 P Florida 33029 (US) 03.12.2010 US 419697 P (74) Representative: Hoffmann Eitle (62) Document number(s) of the earlier application(s) in Patent- und Rechtsanwälte PartmbB accordance with Art. 76 EPC: Arabellastraße 30 11794911.5 / 2 645 993 81925 München (DE) (71) Applicant: ALLERGAN, INC. Remarks: Irvine, CA 92612 (US) •This application was filed on 28-10-2016 as a divisional application to the application mentioned (72) Inventors: under INID code 62. • SHANLER, Stuart D. •Claims filed after the date of receipt of the divisional Pomona application (Rule 68(4) EPC). New York 10970 (US) (54) PHARMACEUTICAL CREAM COMPOSITIONS COMPRISING OXYMETAZOLINE TO TREAT ROSACEA (57) Embodiments relating to cream formulations as baceous glands, such as acne, perioral dermatitis, and well as oxymetazoline creams and methods for treating pseudofolliculitis barbae; disorders of sweat glands, such rosacea and symptoms associated with rosacea, includ- as miliaria, including, but not limited
    [Show full text]