DOCSLIB.ORG

HSI HYDRO-SEARCH, Inc. a Tetra Tech Company

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
HSI HYDRO-SEARCH, Inc. a Tetra Tech Company I HSI HYDRO-SEARCH, inc. A Tetra Tech Company REMEDIAL INVESTIGATION REPORT KINNICKINNIC BUS GARAGE UST AREAS T-1 TIIROUGH T-3 T-4 TIIROUGH T-7, T-9, T-llA AND T-llB l\11LWAUKEE, WISCONSIN August 8, 1996 Prepared for: Milwaukee County Department of Public Works Engineering, Environmental and Energy Services Courthouse Annex, Room #314 907 North 10th Street Milwaukee, Wisconsin 53233 Prepared by: Hydro-Search, Inc. Brookfield Lakes Corporate Center XII 175 N. Corporate Drive, Suite 100 Brookfield, Wisconsin 53045 Michael R. Noel, Sr. Vice President . ass ender, Sr. H ydrogeologist Manager of Milwaukee Operations t Manager 175 N. Corporate Drive, Suite 100, Brookfield, Wisconsin 53045 Telephone (414) 792-1282 Facsimile (414) 792-1310 REMEDIAL INVESTIGATION REPORT KINNICKINNIC BUS GARAGE UST AREAS T-1 THROUGH T-3 T-4 THROUGH T-7, T-9, T-llA AND T-llB MILWAUKEE, WISCONSIN August 8, 1996 was prepared by certified hydrogeologists as defined in NR712.02(1) Wis. Adm. Code I, Judy L. Fassbender, hereby certify that I am a Hydrogeologist as that term is defined in s. NR712.03(1) Wis. Adm. Code, and that, to the best of my knowledge, all of the information contained in this document is correct and the document was prepared in compliance with all applicable requirements in chs. NR700 to 726, Wis. Adm. Code. udy L. Fassbender Senior Hydrogeologist HSI HYDRO-SEARCH, inc. A Tetra Tech Company TABLE OF CONTENTS Page 1.0 EXECUTIVE SUMMARY 1-1 2.0 INTRODUCTION 2-1 2.1 Site History 2-2 2.1.1 UST Area T-1 through T-3 2-2 2.1.2 UST Area T-4 through T-7 and T-9 2-2 2.1.3 UST Area T-llA and T-llB 2-3 3.0 GEOLOGIC AND HYDROGEOLOGIC SETTING 3-1 3.1 Regional Conditions 3-1 3.2 Local Conditions 3-1 4.0 METHODS OF INVESTIGATION 4-1 4.1 UST Area T-1 through T-3 4-1 4.2 UST Area T-4 through T-7 and T-9 4-2 4.3 UST Area T-llA and T-llB 4-3 4.4 Field Investigation Procedures 4-4 5.0 RESULTS 5-1 5.1 UST Area T-1 through T-3 5-1 5.1.1 Soil 5-1 5.1.2 Ground Water 5-1 5.2 UST Area T-4 through T-7 and T-9 5-2 5.3 UST Area T-llA and T-llB - Soil 5-3 1 HSI HYDRO-SEARCH, inc. A Tetra Tech Company TABLE OF CONTENTS (Cont'd) 6.0 CONCLUSIONS AND RECOMMENDATIONS 6-1 6.1 UST Area T-1 through T-3 6-1 6.2 UST Area T-4 through T-7 and T-9 6-1 6.3 UST Area T-llA and T-llB 6-2 FIGURES 1-1 Site Location and Local Topography 2-1 Site Layout 2-2 UST Area T-1 through T-3 Borehole/Monitor Well Locations 2-3 UST Area T-4 through T-7 and T-9 Location Map 2-4 UST Area T-llA and T-llB Borehole Locations 5-1 UST Area T-1, T-2 and T-3 Shallow Water Table Elevation (November 15, 1995) TABLES 5-1 Summary of Soil Laboratory Analytical Results for KK Bus Garage (T-1, T-2, and T-3) 5-2 Summary of Ground-Water Laboratory Analytical Results for KK Bus Garage (T-1 through T-3) 5-3 Summary of Soil Laboratory Analytical Results for KK Bus Garage (T-1 lA and T-1 lB) 11 HSI HYDRO-SEARCH, inc. A Tetra Tech Company TABLE OF CONTENTS (Cont'd) APPENDICES A. WDNR Soil Boring Log Information Forms (4400-122) and Borehole Abandonment Forms (3300-SB) B. Field PID Data Forms and Calibration Record Form C. Laboratory Results and Chain-of-Custody Form D. Monitor Well Construction Forms (4400-113A) and Monitor Well Development Forms (4400-113B) E. Well Development/Purge Summary Forms and Field Water Quality Sampling and Analysis Forms F. Survey Data ll1 HSI HYDRO-SEARCH, inc. A Tetra Tech Company 1. 0 EXECUTIVE SUMMARY The purpose of this investigation was to was to evaluate the nature and extent of contamination of petroleum hydrocarbons in soils and ground water remaining following the upgrading of underground storage tanks (USTs) located at the Kinnickinnic Bus Garage (KKBG) at 1710 South Kinnickinnic Avenue, Milwaukee, Wisconsin (Figure 1-1). The client and property owner is the County of Milwaukee, Wisconsin (County). The remedial investigation was performed by Hydro-Search, Inc. (HSI) and overseen for the County by Mr. Robert L. Knighten, managing environmental engineer for the Milwaukee County Department of Public Works (MCDPW). The scope of the investigation was based upon results obtained and reported by Foth and Van Dyke in their 1992 tank upgrade assessment reports to Mr. Robert Knighten of the MCDPW. These reports documented the excavation required to implement the UST upgrades and the removal and disposal of approximately 1,500 gallons of water at the T-4 through T-7 & T-9 UST area. Soil and water samples collected at the time of UST upgrade indicated contamination was present at levels requiring further investigation. HSI evaluated the current petroleum compound concentrations and the horizontal and vertical extent of petroleum impacted soils and ground-water at three distinct UST areas in October and November of 1995. Soil borehole and monitor well installation along with UST excavation sump sampling were used in the investigation. Borehole installation included field screening of soils with a PID and obtaining soil samples from the borehole for submission to a state­ certified analytical laboratory for analyses. Similarly, ground-water samples were obtained from monitor wells and one UST sump for laboratory submission. Soil and ground-water samples were analyzed for diesel range organics (DROs), petroleum volatile organic compounds (PVOCs), 1,2 DCA, and VOCs as applicable. One soil sample was analyzed for natural biodegradation parameters. None of the soil samples collected contained PVOC or DRO concentrations in excess of the NR720 Residual Contaminant Levels. At the UST area where ground-water monitor wells were installed and ground-water samples collected, no PVOC concentrations above NR140 Preventive Action Limits were detected. Three VOCs were detected at levels above the PAL, but these compounds are believed to be connected with laboratory procedures and not with the petroleum product stored in the USTs (diesel fuel). DRO was detected in the three monitor wells at levels ranging from 565 - 6,980 µgl £. Hydro-Search recommends that natural biodegradation be used to remediate any remaining soil and ground-water contamination at the site. The three site monitor wells should be sampled quarterly for VOCs and DRO for one year. ,If the results indicate sufficiently decreasing levels of contamination in ground water, site closure may be requested unconditionally or conditionally with a deed restriction or incorporating the pending WDNR natural attenuation rules. 1-1 HSI HYDRO-SEARCH, inc. A Tetra Tech Company 2.0 INTRODUCTION The purpose of this investigation was to evaluate the nature and extent of potential soil and ground-water contamination from petroleum hydrocarbons resulting from operations associated with the three UST areas located at the Milwaukee County Transit - Kinnickinnic Bus Garage (KKBG) at 1710 South Kinnickinnic Avenue, Milwaukee, Wisconsin (Figure 2-1). The client and property owner is the County of Milwaukee, Wisconsin (County). The remedial investigation was performed by Hydro-Search, Inc. (HSI) and overseen for the County by Mr. Robert L. Knighten , a civil engineer for the Milwaukee County Department of Public Works (MCDPW). I The scope of the investigation was based upon results obtained and reported by Foth and Van Dyke in their UST compliance upgrade on each UST area. These compliance upgrade reports were included in the Hydro-Search Work Plans for each UST area · (previously submitted; October 2, 1995) and are not reproduced here. UST area T-1 through T-3 consists of three 15 ,000-gallon tanks used to store diesel fuel. UST Area T-4 through T-7 and T-9 consist of one 1,000-gallon engine oil, 2,000-gallon waste oil, 4,000-gallon unleaded gasoline, and two 550-gallon transmission oil and antifreeze tanks, respectively. UST Area T-llA and T-1 lB consist of two 12 ,000-gallon tanks and are also used to store diesel fuel. All of the USTs are constructed of fiberglass and have been in service for approximately 11 years. Each of the UST areas will be described separately in this report. 2-1 HII HYDRO-SEARCH, inc. A Tetra Tech Company 2.1 Site History 2.1.1 UST Area T-1 through T-3 The County owns and operates the KKBG in Milwaukee, Wisconsin, which is used to service County owned mass transit vehicles. A compliance upgrade of the three USTs (Figure 2-2) was performed by Midwest Petroleum Service, Inc. in September 1991. The depth of the excavation was 4 feet below ground surface (bgs). One soil sample was collected from each end of the compliance upgrade excavation and analyzed for total petroleum hydrocarbons-diesel range organics (TPH-DRO). TPH-DRO concentrations in the two samples ranged from 1950 parts per million (ppm) in Tl-PP to 3450 ppm in T2-PP, both of which exceed the WDNR action limits. 2.1.2 UST Area T-4 through T-7 and T-9 In October 1991, Midwest Petroleum Service, Inc. performed a compliance upgrade on all five USTs. Observation of the excavation for the compliance upgrade procedures revealed no petroleum odors, however, soil staining was observed in the southern end of the excavation.
Load more

Recommended publications
  • Classification of Medicinal Drugs and Driving: Co-Ordination and Synthesis Report
    Project No. TREN-05-FP6TR-S07.61320-518404-DRUID DRUID Driving under the Influence of Drugs, Alcohol and Medicines Integrated Project 1.6. Sustainable Development, Global Change and Ecosystem 1.6.2: Sustainable Surface Transport 6th Framework Programme Deliverable 4.4.1 Classification of medicinal drugs and driving: Co-ordination and synthesis report. Due date of deliverable: 21.07.2011 Actual submission date: 21.07.2011 Revision date: 21.07.2011 Start date of project: 15.10.2006 Duration: 48 months Organisation name of lead contractor for this deliverable: UVA Revision 0.0 Project co-funded by the European Commission within the Sixth Framework Programme (2002-2006) Dissemination Level PU Public PP Restricted to other programme participants (including the Commission x Services) RE Restricted to a group specified by the consortium (including the Commission Services) CO Confidential, only for members of the consortium (including the Commission Services) DRUID 6th Framework Programme Deliverable D.4.4.1 Classification of medicinal drugs and driving: Co-ordination and synthesis report. Page 1 of 243 Classification of medicinal drugs and driving: Co-ordination and synthesis report. Authors Trinidad Gómez-Talegón, Inmaculada Fierro, M. Carmen Del Río, F. Javier Álvarez (UVa, University of Valladolid, Spain) Partners - Silvia Ravera, Susana Monteiro, Han de Gier (RUGPha, University of Groningen, the Netherlands) - Gertrude Van der Linden, Sara-Ann Legrand, Kristof Pil, Alain Verstraete (UGent, Ghent University, Belgium) - Michel Mallaret, Charles Mercier-Guyon, Isabelle Mercier-Guyon (UGren, University of Grenoble, Centre Regional de Pharmacovigilance, France) - Katerina Touliou (CERT-HIT, Centre for Research and Technology Hellas, Greece) - Michael Hei βing (BASt, Bundesanstalt für Straßenwesen, Germany).
    [Show full text]
  • Educationally Intervening the Use of Potentially Harmful Medication Among Residents in Institutional Settings
    Department of General Practice and Primary Health Care Faculty of Medicine University of Helsinki Finland EDUCATIONALLY INTERVENING THE USE OF POTENTIALLY HARMFUL MEDICATION AMONG RESIDENTS IN INSTITUTIONAL SETTINGS Anna-Liisa Juola Academic dissertation To be presented, with the permission of the Faculty of Medicine, University of Helsinki, for public examination in Auditorium XII, Fabianinkatu 33, on 2nd February 2018, at 12 noon Helsinki, Finland 2018 Supervisors Professor Kaisu Pitkälä, MD, PhD University of Helsinki, Department of General Practice and Primary Health Care Helsinki, Finland Mikko Björkman, MD, PhD University of Helsinki, Department of Medicine, Division of Geriatrics Helsinki, Finland Reviewers Professor Esa Leinonen, MD, PhD University of Tampere, Department of Psychiatry Tampere, Finland Adjunct Professor Juha Puustinen, MD, PhD University of Helsinki, Division of Pharmacology and Pharmacotherapy Helsinki, Finland Satakunta Hospital District, Unit of Neurology Pori, Finland Opponent Adjunct Professor Raimo Isoaho, MD, MPH, PhD University of Turku, Department of General Practice Turku, Finland City of Vaasa, Social and Health Services Vaasa, Finland Cover graphics Vesa Juola Untitled 2017 ISBN 978-951-51-4032-6 (nid.) ISBN 978-951-51-4033-3 (PDF) Unigrafia Helsinki 2018 To Vesa with love Contents Abbreviations 7 Definitions 8 List of original publications 9 Abstract 10 Tiivistelmä (Finnish Abstract) 13 1 Introduction 17 2 Review of the literature 19 2.1 Ageing and medication 19 2.1.1 Pharmacokinetics
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 8,828,437 B2 Sundberg Et Al
    USOO8828437B2 (12) United States Patent (10) Patent No.: US 8,828,437 B2 Sundberg et al. (45) Date of Patent: *Sep. 9, 2014 (54) THERMOGELLING ANAESTHETIC USPC .......................................................... 424/484 COMPOSITIONS (58) Field of Classification Search None (71) Applicant: Pharmanest AB, Solna (SE) See application file for complete search history. (72) Inventors: Mark Sundberg, Arsta (SE); Arne (56) References Cited Brodin, Sodertalje (SE); Nils Kallberg, Taby (SE) U.S. PATENT DOCUMENTS (73) Assignee: Pharmanest AB, Solna (SE) 8,663,688 B2* 3/2014 Fernandez et al. ............ 424/487 2004/O220283 A1 11/2004 Zhang et al. 2005/0O27.019 A1 2/2005 Zhang et al. (*) Notice: Subject to any disclaimer, the term of this 2007/0298.005 A1 12, 2007 Thibault patent is extended or adjusted under 35 2008. O15421.0 A1 6/2008 Jordan et al. U.S.C. 154(b) by 0 days. 2012fO294907 A1 11/2012 Zhang et al. This patent is Subject to a terminal dis claimer. FOREIGN PATENT DOCUMENTS AU 2006201233 B2 10, 2007 (21) Appl. No.: 14/172,794 EP O517160 A1 12, 1992 EP 1629852 A2 3, 2006 (22) Filed: Feb. 4, 2014 KR 2002OO13248 A 2, 2002 (65) Prior Publication Data (Continued) OTHER PUBLICATIONS US 2014/O155.434 A1 Jun. 5, 2014 Written Opinion, Intellectual Property Office of Singapore, from the Related U.S. Application Data corresponding Singapore Application No. 201206824-3, Jul. 19. (63) Continuation of application No. 13/638.511, filed as 2013. application No. PCT/EP2011/055009 on Mar. 31, Notification of First Office Action, China Intellectual Property 2011. Office, from the corresponding Chinese Application No.
    [Show full text]
  • ZUSAMMENFASSUNG DER MERKMALE DES ARZNEIMITTELS & PACKUNGSBEILAGE SEVORANE 1. BEZEICHNUNG DES ARZNEIMITTELS Sevorane Quick Fi
    ZUSAMMENFASSUNG DER MERKMALE DES ARZNEIMITTELS & PACKUNGSBEILAGE SEVORANE 1. BEZEICHNUNG DES ARZNEIMITTELS Sevorane Quick Fill 100%, Flüssigkeit zur Herstellung eines Dampfs zur Inhalation 2. QUALITATIVE UND QUANTITATIVE ZUSAMMENSETZUNG Sevofluran 100% Vollständige Auflistung der sonstigen Bestandteile siehe Abschnitt 6.1. 3. DARREICHUNGSFORM Flüssigkeit zur Herstellung eines Dampfs zur Inhalation Eigenschaften: Sevoflurane ist ein fluoriertes Derivat von Methylisopropylether. Sevoflurane wird chemisch als Fluormethyl 2,2,2-trifluor-1-(trifluormethyl) Ethylether identifiziert und hat ein Molekulargewicht von 200,05. Sevoflurane besitzt folgende physikalische und chemische Eigenschaften: Siedepunkt bei 760 mm Hg 58,6°C Dichte bei 20°C 1,520-1,525 Dampfspannung (errechnet) in mm HG** 157 mm Hg bei 20°C 197 mm Hg bei 25°C 317 mm Hg bei 36°C ** Gleichung für die (errechnete) Dampfspannung, mm Hg: Log10Pvap = A+B/T wobei: A = 8,086 B = -1726,68 T = °C + 273,16°K (Kelvin) Verteilungskoeffizienten bei 37°C Blut/Gas 0,63-0,69 Wasser/Gas 0,36 Olivenöl/Gas 47,2-53,9 Gehirn/Gas 1,15 Mittlere Verteilungskoeffizienten, Bestandteil/Gas bei 25°C für Polymere, die häufig bei medizinischen Anwendungen angewendet werden; Leitfähiger Gummi 14,0 Butylkautschuk 7,7 Polyvinylchlorid 17,4 Polyethylen 1,3 Sevoflurane ist nicht entflammbar und nicht explosiv entsprechend der Norm 601-2-13 der Internationalen Elektrotechnik-Kommission. Sevoflurane ist eine klare und farblose Flüssigkeit. ZMA = Leaflet (DE) 1/17 printed on 4-Feb-19 16:03 Sevoflurane ist nicht reizend. Es ist mischbar mit Ethanol, Ether, Chloroform und Benzol und im Wasser schwach löslich. Abbau von Sevofluran Sevoflurane ist stabil, wenn es bei normalen Lichtbedingungen gelagert wird.
    [Show full text]
  • Holland & Knight
    FILED 1/14/2020 DOCUMENT NO. 00281-2020 Holland & Knight FPSC - COMMISSION CLERK 315 South Calhoun Street, Suite 600 I Tallahassee, FL 32301 IT 850.224.7000 I F 850.224.8832 Holland & Knight LLP I www.hklaw.com D. Bruce May, Jr. (850) 425-5607 [email protected] January 14, 2020 Adam Teitzman Office of Commission Clerk Florida Public Service Commission 2540 Shumard Oak Boulevard Tallahassee, FL 32399-0850 Re: Docket 20190194-WS -- Application for original water and wastewater and approval of initial rates, charges and standard service agreements in Lee County, by CPI Citrus Park Utility TRS, L.L.C. Dear Mr. Teitzman: CPI Citrus Park Utility TRS, L.L.C. (the "Utility") respectfully submits its responses to Commission Staffs letter dated November 21, 2019 ("Staff Letter"), which identified certain deficiencies to the Utility's application submitted on October 23, 2019. For ease ofreference, the deficiencies set forth in the Staff Letter are repeated verbatim herein, with the Utility's response immediately following each item. I. Contact info. Rule 25-30.033(1 )(c), Florida Administrative Code (F.A.C.), requires the utility's name, address, telephone number, Federal Employer Identification Number, authorized representative, and, if available, email address and fax number. Please provide the Utility's email, fax number, and telephone number, if different from the telephone number provided for Mr. David Daniel, as a contact for the application. Response: The Utility's email address is: [email protected]. The relevant contact information regarding the application is as follows: Steven P. Adler 12629 New Brittany Blvd.
    [Show full text]
  • Evaluation of Carcinogenicity Studies of Medicinal Products for Human Use Authorised Via the European Centralised Procedure
    Regulatory Toxicology and Pharmacology xxx (2011) xxx–xxx Contents lists available at ScienceDirect Regulatory Toxicology and Pharmacology journal homepage: www.elsevier.com/locate/yrtph Evaluation of carcinogenicity studies of medicinal products for human use authorised via the European centralised procedure (1995–2009) ⇑ Anita Friedrich a, , Klaus Olejniczak b a Granzer Regulatory Consulting and Services, Zielstattstrasse 44, 81379 Munich, Germany b Federal Institute for Drugs and Medical Devices, Kurt-Georg-Kiesinger-Allee 3, 53175 Bonn, Germany article info abstract Article history: Carcinogenicity data of medicinal products for human use that have been authorised via the European Received 25 October 2010 centralised procedure (CP) between 1995 and 2009 were evaluated. Carcinogenicity data, either from Available online xxxx long-term rodent carcinogenicity studies, transgenic mouse studies or repeat-dose toxicity studies were available for 144 active substances contained in 159 medicinal products. Out of these compounds, 94 Keywords: (65%) were positive in at least one long-term carcinogenicity study or in repeat-dose toxicity studies. Medicinal products Fifty compounds (35%) showed no evidence of a carcinogenic potential. Out of the 94 compounds with Carcinogenicity positive findings in either carcinogenicity or repeat-dose toxicity studies, 33 were positive in both mice Rodents and rats, 40 were positive in rats only, and 21 were positive exclusively in mice. Long-term carcinogenic- ity studies in two rodent species were available for 116 compounds. Data from one long-term carcinoge- nicity study in rats and a transgenic mouse model were available for eight compounds. For 13 compounds, carcinogenicity data were generated in only one rodent species. One compound was exclu- sively tested in a transgenic mouse model.
    [Show full text]
  • Summary of Product Characteristics
    Health Products Regulatory Authority Summary of Product Characteristics 1 NAME OF THE MEDICINAL PRODUCT Versatis 700 mg medicated plaster 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each 10 cm x 14 cm plaster contains 700 mg lidocaine (equivlent to 5% w/w) Excipients with known effect: Methyl parahydroxybenzoate (E218) 14 mg Propyl parahydroxybenzoate (E216) 7 mg Propylene glycol (E1520) 700 mg For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Medicated plaster White hydrogel plaster containing adhesive material, which is applied to a non-woven polyethylene terephthalate backing embossed with “Lidocaine 5%” and covered with a polyethylene terephthalate film release liner. 4 CLINICAL PARTICULARS 4.1 Therapeutic Indications Versatis is indicated for the symptomatic relief of neuropathic pain associated with previous herpes zoster infection (post-herpetic neuralgia, PHN) in adults. 4.2 Posology and method of administration Adults and elderly patients The painful area should be covered with the plaster once daily for up to 12 hours within a 24 hours period. Only the number of plasters that are needed for an effective treatment should be used. When needed, the plasters may be cut into smaller sizes with scissors prior to removal of the release liner. In total, not more than three plasters should be used at the same time. The plaster must be applied to intact, dry, non-irritated skin (after healing of the shingles). Each plaster must be worn no longer than 12 hours. The subsequent plaster-free interval must be at least 12 hours. The plaster can be applied during the day or during the night.
    [Show full text]
  • Scandonest EMEA/H/A30/1455
    Annex I List of medicinal products and presentations 1 Member State Marketing authorisation Invented Name Strength Pharmaceutical Route of Content EU/EEA holder form administration (concentration) SCANDONEST 3% Septodont GmbH OHNE Felix-Wankel-Str. 9 Solution for Austria VASOKONSTRIKTOR 3% Dental use 30 mg/ml 53859 Niederkassel-Mondorf injection - Germany ZYLINDERAMPULLEN Septodont NV-SA SCANDONEST 3% 87 Avenue de la Constitution Solution for Belgium SANS 3% Dental use 30 mg/ml B-1083 Bruxelles injection VASOCONSTRICTEUR Belgium Septodont 58, rue du Pont de Créteil SCANDONEST 30 Solution for Bulgaria 30 mg/ml Dental use 30 mg/ml 94100 Saint-Maur-des-Fossés MG/ML injection France Apolonia d.o.o. SCANDONEST 30 Dental use Dubrova 308 Solution for Croatia mg/ml otopina za 30 mg/ml Perineural use 30 mg/ml 52220 Labin injection injekciju Submucosal use Croatia Spécialités Septodont Dental use 58, rue du Pont de Créteil Solution for Denmark SCANDONEST 30 mg/ml Perineural use 30 mg/ml 94100 Saint-Maur-des-Fossés injection Submucosal use France Septodont Solution for Dental use 58, rue du Pont de Créteil Estonia SCANDONEST 30 mg/ml injection in Perineural use 30 mg/ml 94100 Saint-Maur-des-Fossés cartridge Submucosal use France Septodont 58, rue du Pont de Créteil Solution for Dental use Finland SCANDONEST 30 mg/ml 30 mg/ml 94100 Saint-Maur-des-Fossés injection France Laboratoires Septodont SCANDONEST 30 58, rue du Pont de Créteil Dental use MG/ML, SOLUTION Solution for France 94107 Saint-Maur-des-Fossés 30 mg/ml Perineural use 30 mg/ml INJECTABLE À injection Cedex Submucosal use USAGE DENTAIRE France 2 Member State Marketing authorisation Invented Name Strength Pharmaceutical Route of Content EU/EEA holder form administration (concentration) Septodont GmbH SCANDONEST 3% Felix-Wankel-Str.
    [Show full text]
  • 2Ull/121Uo2 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 Χ / A 1 6 October 2011 (06.10.2011) W O 2Ull/121Uo2 Al (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every A61K 9/06 (2006.01) A61K 31/445 (2006.01) kind of national protection available): AE, AG, AL, AM, A61K 9/00 (2006.01) AO, AT, AU, AZ, BA, BB, BG, BH, BR, BW, BY, BZ, 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/EP201 1/055025 HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, (22) International Filing Date: KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, 31 March 201 1 (3 1.03.201 1) ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, 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, TH, TJ, TM, TN, TR, (26) Publication Language: English TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: (84) Designated States (unless otherwise indicated, for every 1050322-5 1 April 2010 (01 .04.2010) SE kind of regional protection available): ARIPO (BW, GH, 61/325,425 19 April 2010 (19.04.2010) US GM, KE, LR, LS, MW, MZ, NA, SD, SL, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, MD, RU, TJ, (71) Applicant (for all designated States except US): Phar- TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, manest AB [SE/SE]; Karolinska Institutet Science Park, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, Nobels vag 3, S-171 65 Solna (SE).
    [Show full text]
  • Australian Statistics on Medicines 2009
    Australian Statistics on Medicines 2009 Australian Statistics on Medicines 2009 Acknowledgments Prepared by Vanna Mabbott, Maxine Robinson and Quinton Brennan of the Drug Utilisation Sub-Committee Secretariat. We would like to thank the following people for their help in the access and provision of data and information used in this report: • The World Health Organization Collaborating Centre for Drug Statistics Methodology. • Jess Dalla, Jennifer Haigh and Zoe Holdenson, Special Access Programs and Special Access Programs 2, Department of Health and Ageing. • Elspeth Kay, Adverse Drug Reaction Advisory Committee, Therapeutic Goods Administration. • Jacqueline Rek, Australian Institute of Health and Welfare. Australian Statistics on Medicines 2009 Print ISBN: 978-1-74241-557-4 Online ISBN: 978-1-74241-558-1 Publications approval number: D0514 Paper-based publications © Commonwealth of Australia 2011 This work is copyright. You may reproduce the whole or part of this work in unaltered form for your own personal use or, if you are part of an organisation, for internal use within your organisation, but only if you or your organisation do not use the reproduction for any commercial purpose and retain this copyright notice and all disclaimer notices as part of that reproduction. Apart from rights to use as permitted by the Copyright Act 1968 or allowed by this copyright notice, all other rights are reserved and you are not allowed to reproduce the whole or any part of this work in any way (electronic or otherwise) without first being given the specific written permission from the Commonwealth to do so. Requests and inquiries concerning reproduction and rights are to be sent to the Communications Branch, Department of Health and Ageing, GPO Box 9848, Canberra ACT 2601, or via e-mail to [email protected].
    [Show full text]
  • Scandonest EMEA/H/A30/1455
    Annex III Product information Note: This product information is the outcome of the referral procedure to which this Commission decision relates. The product information may be subsequently updated by the Member State competent authorities, in liaison with the reference Member State, as appropriate, in accordance with the procedures laid down in Chapter 4 of Title III of Directive 2001/83/EC. 11 SUMMARY OF PRODUCT CHARACTERISTICS 12 1. NAME OF THE MEDICINAL PRODUCT {Scandonest and associated names (see Annex I) strength pharmaceutical form} [See Annex I - To be completed nationally] 2. QUALITATIVE AND QUANTITATIVE COMPOSITION 1 ml solution for injection contains 30 mg of mepivacaine hydrochloride. Each cartridge of 1.7 ml of solution for injection contains 51 mg of mepivacaine hydrochloride. Each cartridge of 2.2 ml of solution for injection contains 66 mg of mepivacaine hydrochloride. Excipient(s) with known effect Each ml contains 0.11 mmol of sodium (2.467 mg/ml). For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Solution for injection. Clear and colourless solution. PH: 6.1-6.7 4. CLINICAL PARTICULARS 4.1 Therapeutic indications {Scandonest and associated names (see Annex I) strength pharmaceutical form} is a local anaesthetic indicated for the local and loco-regional anaesthesia in dental surgery in adults, adolescents and children above 4 years of age (c.a. 20 kg of body weight). 4.2 Posology and method of administration The medicinal product should only be used by or under the supervision of dentists, stomatologists or other clinicians sufficiently trained and familiar with diagnosis and treatment of systemic toxicity.
    [Show full text]
  • Inventory of the Most Important Pharmaceutical Compounds
    018530 - SWITCH Sustainable Water Management in the City of the Future Integrated Project Global Change and Ecosystems Deliverable 4.1.2 Listing the most important pharmaceutical compounds from various therapeutic groups and the testing and validation of analytical methods for the selected compounds 4.1.2 A. Pre-selection of representative compounds for laboratory degradation tests 4.1.2 B Survey of the mostly used pharmaceutical compounds and hormones in the West Bank/Palestine 4.1.2 C. Estrogens in aquatic environment: A review. Due date of deliverable: 14 th February 2007 Actual submission date: 14 th February 2007 Start date of project: 1 February 2006 Duration: 60 months Authors : Katarzyna Kujawa-Roeleveld, Ime Akanyeti WU, Environmental Technology, Wageningen, The Netherlands Nidal Mahmoud, Water Studies Institute (WSI), Birzeit University, The West Bank, Palestine Wenxin Shi, IHE-UNESCO, Delft, The Netherlands Final Version Reviewer: Adriaan Mels Project co-funded by the European Commission within the Sixth Framework Programme (2002-2006) Dissemination Level PU Public Pu PP Restricted to other programme participants (including the Commission Services) RE Restricted to a group specified by the consortium (including the Commission Services) CO Confidential, only for members of the consortium (including the Commission Services) 1 SWITCH Deliverable Briefing Note (months 0-12) SWITCH Document Deliverable 4.1.2 consists of three parts: (A) Pharmaceutical compounds in environment Pre-selection of representative compounds for laboratory degradation tests (B) Survey of the mostly used pharmaceutical compounds and hormones in the West Bank/ Palestine (C) Estrogens in aquatic environment: A review Audience This document is targeted at scientists, engineers and policy makers.
    [Show full text]