Примери за използване на Pegasys treatment на Английски и техните преводи на Български
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Group A(Pegasys treatment)(N=101).
In chronic hepatitis B the duration of Pegasys treatment is 48 weeks.
Pegasys treatment should be discontinued in patients who develop new or worsening ophthalmologic disorders.
Patients with advanced fibrosis were assigned to Pegasys treatment(group C, n=10).
Once you have started Pegasys treatment, talk to your doctor, nurse or pharmacist.
Table 24: HBeAg seroconversion rates(%)by HBV-DNA decline from baseline to week 12 of Pegasys treatment in paediatric patients.
Pegasys treatment may be initiated or continued if TSH levels can be maintained in the normal range by medication.
Transplantation The safety and efficacy of Pegasys treatment have not been established in patients with liver transplantation.
Other published on-treatment biomarkers that are predictive of the final outcome of Pegasys treatment may be considered.
Pegasys treatment was associated with decreases in absolute CD4+ cell counts within the first 4 weeks without a reduction in CD4+ cell percentage.
Adverse events orlaboratory abnormalities led to 5% of patients withdrawing from Pegasys treatment, while less than 1% of patients withdrew from lamivudine treatment for these reasons.
Pegasys treatment was associated with clinically significant abnormalities in thyroid laboratory values requiring clinical intervention(see section 4.4).
Similarly for patients with cirrhosis or transition to cirrhosis,the frequencies of withdrawal from Pegasys treatment and ribavirin treatment were higher in the 72-week treatment arms(13% and 15%) than in the 48-week arms(6% and 6%).
Pegasys treatment has been associated with decreases in platelet count, which returned to pretreatment levels during the post-treatment observation period(see section 4.8).
In a clinical trial of non-responder patients to prior pegylated interferon alfa-2b/ ribavirin, which exposed patients to either 48 or72 weeks of treatment, the frequency of withdrawal for adverse events or laboratory abnormalities from Pegasys treatment and.
(copies/mL)/ 5.26** Patients switched to Pegasys treatment post-principal observation period and before Week 24 follow-up were counted as non-responders.
In a clinical trial of non-responder patients to prior pegylated interferon alfa-2b/ ribavirin, which exposed patients to either 48 or 72 weeks of treatment, the frequency of withdrawal for adverse events orlaboratory abnormalities from Pegasys treatment and ribavirin treatment was 6% and 7%, respectively, in the 48 week arms and 12% and 13%, respectively.
In clinical trials, Pegasys treatment was associated with decreases in both total white blood cell(WBC) count and ANC, usually starting within the first 2 weeks of treatment(see section 4.8).
In a clinical trial of non-responder patients to prior pegylated interferon alfa-2b/ ribavirin, which exposed patients to either 48 or 72 weeks of treatment, the frequency of withdrawal for adverse events orlaboratory abnormalities from Pegasys treatment and ribavirin treatment was 6% and 7%, respectively, in the 48 week arms and 12% and 13%, respectively, in the 72 week arms.
In clinical trials, Pegasys treatment was associated with decreases in both total white blood cell(WBC) count and absolute neutrophil count(ANC), usually starting within the first 2 weeks of treatment(see section 4.8).
Pegasys treatment was associated with abnormal laboratory values: ALT increase, bilirubin increase, electrolyte disturbance(hypokalaemia, hypocalcaemia, hypophosphataemia), hyperglycaemia, hypoglycaemia and elevated triglycerides(see section 4.4.).
At Week 48 of Pegasys treatment, a height or weight percentile decrease of more than 15 percentiles on the normative growth curves was observed in 6% of patients for height and 11% of patient for weight, whereas in the untreated group it was 2% of patients for height and 9% for weight.
Treatment with Pegasys should be discontinued immediately in patients with hepatic decompensation.
Liver function In patients who develop evidence of hepatic decompensation during treatment, Pegasys should be discontinued.
It is important to consider the treatment with Pegasys+/- ribavirin induced a growth inhibition during treatment, the reversibility of which is uncertain.
The duration of treatment with Pegasys in combination with ribavirin in paediatric patients with CHC depends on viral genotype.
Patients in group B had the choice to switch to treatment with Pegasys after Week 48 of the principal observation period.
The safety and efficacy of Pegasys and ribavirin treatment have not been established in patients with liver and other transplantations.
Suicidal ideation is identified,it is recommended that treatment with Pegasys be discontinued, and the patient followed, with psychiatric intervention as appropriate.
Pegasys is best used for this treatment in combination with ribavirin.