La tétracycline, connue sous le nom commercial Sumycin, agit en bloquant la fixation de l’ARNt sur la sous-unité 30S ribosomale, interrompant l’élongation de la chaîne protéique bactérienne. Ce mécanisme confère une activité sur un spectre large, incluant bactéries Gram positives, Gram négatives, rickettsies et spirochètes. Sa biodisponibilité digestive varie selon la prise alimentaire et les interactions avec les ions divalents comme calcium et magnésium. Sa diffusion tissulaire est importante, notamment dans les voies respiratoires et génito-urinaires. L’élimination se fait par voie rénale et biliaire. Les effets indésirables incluent photosensibilisation, troubles digestifs et coloration dentaire en cas d’administration précoce. Les guides thérapeutiques mentionnent sumycin prix, en soulignant la nécessité de restreindre son utilisation afin de limiter les résistances acquises.
C:\documents and settings\administrator\my documents\giannini\notes&memos\questionnaire.wpd
LAW OFFICES OF PATRICK E. CATALANO A PROFESSIONAL CORPORATION SAN DIEGO OFFICE SAN FRANCISCO OFFICE The Koll Center 781 Beach Street, Suite 333 501 West Broadway, Suite 740 San Francisco, California 94109 San Diego, California 92101-3544 (415) 788-0207 (619) 233-3565 Fax: (415) 447-0066 Fax: (619) 233-9841 Charles S. LiMandri, Esq. Nicholas A. Siciliano, Esq. LAW OFFICES OF CHARLES S. LiMANDRI LAW OFFICES OF MASRY & VITITOE P.O. Box 9120 A Professional Corporation 16236 San Dieguito Road 5707 Corsa Avenue, Second Floor Building 3, Suite 3-15 Westlake Village, California 91362 Rancho Santa Fe, California 92067 (818) 991-8900 (858) 759-9930 Fax: (818) 991-6200 Fax: (858) 759-9938 CLIENT QUESTIONNAIRE Ann Giannini, et. al. v. Schering-Plough, et. al.
Client Name:______________________________________________________________
Date of diagnosis of Hepatitis C:__________________________________________
Genotype:____________________________________________________________
Viral Load (if known):__________________________________________________
Severity and type of Hepatitis C symptoms (mild, moderate, severe) prior totreatment:__________________________________________________________
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Other medical conditions at the time of diagnosis:___________________________
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Who suggested PEG-Intron and/or Rebetol treatment?_________________________
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Was Schering-Plough the manufacturer of the PEG-Intron and/or Rebetolused?______________________________________________________________
Client QuestionnairePage 2_______________________
Did your physician describe the potential risks and benefits of this therapy?
say?_____________________________________________
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Did your physician describe the types of serious reactions you might experience?
If yes, what were these adverse reactions?___________________________________
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Date PEG-Intron and/or Rebetol therapy started:______________________________
Where was the PEG-Intron and/or Rebetol obtained? Please state the name, addressand telephone number of the pharmacy:____________________________________
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Do you have any paperwork regarding the order of PEG-Intron and/or Rebetol? Ifyes, please attach.
Were you told to wait to begin therapy until a new form of Intron was available fortreatment?__________________________________________________________
If yes, how long did you wait?__________________________________________
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Date PEG-Intron and/or Rebetol therapy stopped:_____________________________
Was Rebetol (ribavirin) also prescribed and if so what was the dosage?___________
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Client QuestionnairePage 3_______________________
Please list other medications taken at the same time:___________________________
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Dat e o f f i r s t a d v e r s e re a c t i on t o PEG- I n t ron and/or Rebetol:____________________________________________________________
How long were you treated before your adverse reactions started?_______________
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Please list the adverse reactions and note their severity:________________________
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Do you still have these adverse reactions?__________________________________
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Have these adverse reactions become less or more severe?______________________
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Are these adverse reactions disabling?_____________________________________
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Were you hospitalized because of these adverse reactions?_____________________
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Client QuestionnairePage 4_______________________
Why do you think PEG-Intron and/or Rebetol caused these symptoms?____________
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Did your physician adjust your dose or discontinue treatment after you reported thesesymptoms to him/her?___________________________________________________
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Did you report the adverse reactions(s) to the drug company and, if so, which drugcompany (name, address, telephone number)?________________________________
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If yes, how did the drug company respond?__________________________________
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Did you report the adverse reaction(s) to the FDA or to anyone else and, if so, pleaselist in detail:__________________________________________________________
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Client QuestionnairePage 5_______________________
Do you know the lot numbers of any of the PEG-Intron and/or Rebetol or ribavirintreatments you took and, if so, please list:__________________________________
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How did you obtain your Intron or PEG-Intron and/or Rebetoldrug?_______________________________________________________
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Identify by batch and lot number the PEG-Intron and/or Rebetolused?______________________________________________________________
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Professor Robert A Cocks Publications in peer reviewed journals Cocks R A. Study of 100 patients injured by London Underground Trains 1981-1986. British Medical Journal 1987; 295: 1527-1529. Cocks R A. Trauma in the tube - the problems of railway suicide and its consequences. Stress Medicine 1989; 5: 93-97. Cocks R A., Yates D W. How to perform diagnostic peritoneal lavage. British Journ
Media Contact: Karina GAJEK +33 (0)1 40 33 11 30 media.relations@hra-pharma.com Ulipristal acetate (ellaOne®) significantly reduces pregnancy risk versus levonorgestrel for oral emergency contraception European Medicines Agency confirms findings from HRA Pharma’s most recent data Paris, France July 15, 2010 - HRA Pharma announced today that the European Medicines Agency