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18 résultats avec le mot-clé: 'safety efficacy daclatasvir sofosbuvir hcv genotype infected patients'

Safety and efficacy of daclatasvir-sofosbuvir in HCV genotype 1-mono-infected patients

Conclusion The sofosbuvir+daclatasvir combination is associated with a high rate of SVR12 in patients infected by genotype 1, with an optimal duration of 12 weeks in non-cirrhotic and

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Real-world efficacy and safety of direct-acting antiviral drugs in patients with chronic hepatitis C and inherited blood disorders

The first patient was a 59-year-old female infected with HCV genotype 2 receiving sofosbuvir and daclatasvir who stopped treatment at 18 days of administration due to adverse

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Efficacy and Safety of Sofosbuvir plus Daclatasvir for Treatment of HCV-associated Cryoglobulinemia Vasculitis.

Thirty-seven patients (90.2%) had a complete clinical response (defined by improvement of all the affected organs involved at baseline and no clinical relapse) after

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Sofosbuvir and Ribavirin in HCV Genotypes 2 and 3

For patients infected with HCV genotype 3, extending sofosbuvir–ribavirin treatment to 24 weeks resulted in substantially higher rates of response and lower rates of re- lapse

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Notes du cours de Th´eorie des Automates Licence 3 Ann´ee 2012-2013

On remarquera qu’il y a deux arˆ etes de 2 vers 1 avec l’´ etiquette a, c’est donc ici que les triplets “(source, lettre, but)” ne s´ eparent pas les arˆ etes.. 4 et faire

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Safety and efficacy of the combination simeprevir-sofosbuvir in HCV genotype 1- and 4-mono-infected patients from the French ANRS CO22 hepather cohort

Most patients (81%) received the sofosbu- vir/simeprevir combination without ribavirin for 12 weeks with a SVR of 93%. No significant difference in SVR12 rate was found between 12 or

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The effectiveness of daclatasvir based therapy in European patients with chronic hepatitis C and advanced liver disease

In recent Phase 2 and 3 studies, the treatment combination of daclatasvir and sofosbuvir achieved a rate of SVR12 above 95% in genotype 1 patients without cirrhosis [8]; rates above

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Of Time and Trauma: The Possibilities for Narrative in Paula Gunn Allen’s The Woman Who Owned the Shadows

In Allen’s narrative, this disruption of collective narratives by Ephanie’s personal trauma serves to underline the distinction between the destructive white narratives that

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Lingüística Aplicada y Didáctica del Español, del Portugués y del I...

Doctorandas: Aicha Assafi, Dina Laghmari, Halima Aaddi y Marta

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Hepatic steatosis in HIV-HCV coinfected patients receiving antiretroviral therapy is associated with HCV-related factors but not antiretrovirals.

In conclusion, for our Caucasian cohort predomin- antly infected with genotype-HCV 1, hepatic steatosis in HIV-HCV coinfected patients receiving antiretroviral therapy is

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Apport de l'angioscanner dans la prise en charge des lésions artérielles thoraco-abdominales dans le service d'imagerie médicale et de médecine nucléaire au CHU du Point G

Les anévrysmes de l’aorte abdominale sont dans la très grande majorité des cas d’origine athéroscléreuse. Cependant, le développement de la formation anévrysmale est

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GUIDE PRATIQUE DE L’ENSEIGNANT  VACATAIRE

Velocity profiles decrease when magnetic parameter M increases, but the profiles increase with M after a certain point for the assisting flow.. 1 Physical model and coordinate

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ECA launches an African technology network to generate value from research and development

Addis Ababa, 17 June 2010 (ECA) - The United Nations Economic Commission for Africa (ECA) has launched a network of community of experts and institutions involved in

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Prescription and efficacy of daclatasvir and sofosbuvir +/- ribavirin for hepatitis C infection, including patient-reported outcomes, in routine practice in three European countries: the CMPASS-EU cohort study.

Cite this article as: Prescription and efficacy of daclatasvir and sofosbuvir ± ribavirin for hepatitis C infection, includ- ing patient-reported outcomes, in routine practice in

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Ledipasvir and Sofosbuvir for Previously Treated HCV Genotype 1 Infection

Law itz reports receiving consulting fees from AbbVie, Achillion Pharmaceuticals, Idenix Pharmaceuticals, Janssen Pharmaceuticals, Novartis, Merck, Vertex Pharmaceuticals,

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PRISE EN CHARGE DE L'HEPATITE C EN 2019: PLACE DU GENOTYPAGE

High Efficacy in Patients With Chronic Hepatitis C Virus (HCV) Genotype (GT)1b Infection Treatment With Elbasvir/Grazoprevir for 12 Weeks: An Integrated

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Instruction n° DGOS/PF2/DGS/SP2/DSS/1C/2017/246 du 3 août 2017 relative à l’élargissement de la prise en charge par l’assurance maladie du traitement de l’hépatite C par les nouveaux agents anti-viraux d’action directe (AAD) à tous les stades de fibrose h

Pour les spécialités SOVALDI ® (sofosbuvir), DAKLINZA ® (daclatasvir), HARVONI ® (sofosbuvir/ledipatasvir), VIEKIRAX ® (ombitasvir-paritaprévir-ritonavir), EXVIERA ®

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نظام الحصص النسائية وتأ ثيره على التمثيل ا لس ياسي للمرأ ة المغاربية في المجالس المجلية المنتخبة

لابقع ـسم اـهرفوت نكألماو ةحاعلما ةيع لمجاو ةيسمرلا تناماضلا همم يضوت لىا اضيم ة ارلا فد ماك كلا في ماــظن دــتو لــعفُت نم

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