Примери за използване на Treatment with soliris на Английски и техните преводи на Български
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No paediatric patient required new dialysis during treatment with Soliris.
Anticoagulant therapy Treatment with Soliris should not alter anticoagulant management.
Six out of seven patients did not need any transfusionof red blood cells, and haemoglobin levels improved during 12 weeks of treatment with Soliris.
Interactions between your treatment with Soliris and food or drink are unlikely.
Treatment with Soliris improved patients' symptoms and their ability to undertake daily activities based on a standard scoring system.
Pregnancy Tell your doctor before starting treatment with Soliris if you are pregnant or plan to become pregnant.
Treatment with Soliris consists of an intravenous infusion(drip into a vein) of 600 mg over 25 to 45 minutes once a week, followed by 900 mg in the fifth week.
Patients received meningococcal vaccination prior to initiating treatment with Soliris or received prophylactic treatment with appropriate antibiotics until 2 weeks after vaccination.
Treatment with Soliris over 26 weeks led to stable haemoglobin levels in 49% of the patients(21 out of 43), without the need for transfusions of red blood cells.
Patients either received meningococcal vaccination at least 2 weeks prior to initiating treatment with Soliris or received prophylactic treatment with appropriate antibiotics until 2 weeks after vaccination.
Longer term treatment with Soliris(median 52 weeks ranging from 15 to 126 weeks) was associated with an increased rate of clinically meaningful improvements in adult patients with aHUS.
If your child is below the age of vaccination or if you are not vaccinated at least 2 weeks before you start treatment with Soliris, your doctor will prescribe antibiotics to reduce the risk of infection until 2 weeks after you have been vaccinated.
The study found that treatment with Soliris for 6 months led to clinically meaningful reductions in levels of LDH, indicating reduced breakdown of red blood cells.
Patients that were previously treated with Soliris in Study ECU-MG-301 continued to demonstrate a sustained effect of Soliris on all measures(MG-ADL, QMG, MGC and MG-QoL15)over an additional 52 weeks of treatment with Soliris.
Interrupting or stopping treatment with Soliris may cause your gMG symptoms to come back.
The second study, involving 20 patients with aHUS who were already receiving plasma exchange or infusion, resulted in 80% of the patients nolonger requiring plasma exchange, infusion or dialysis and 90% of the patients achieving haematological normalisation after treatment with Soliris.
Interrupting or ending treatment with Soliris may cause your aHUS symptoms to come back.
Treatment with Soliris increased platelet counts in 82% of the patients, and platelet counts rose to normal levels in 87%(13 out of 15 patients) who had low platelet counts at the start.
Interrupting or stopping treatment with Soliris may cause your NMOSD to worsen and relapse to happen.
Longer term treatment with Soliris(median 55 weeks ranging from 1day to 107 weeks) was associated with an increased rate of clinically meaningful improvements in paediatric and adolescent patients with aHUS.
Patients who discontinue treatment with Soliris should be monitored for signs and symptoms of serious intravascular haemolysis.
Interrupting or ending treatment with Soliris may cause your PNH symptoms to come back more severely soon.
If PNH patients discontinue treatment with Soliris they should be closely monitored for signs and symptoms of serious intravascular haemolysis.
If aHUS patients discontinue treatment with Soliris, they should be monitored closely for signs and symptoms of severe thrombotic microangiopathy complications.
At least 14 days before you start treatment with Soliris, your doctor will administer a vaccine against meningitis if it was not previously administered or if your vaccination is outdated.
At least 2 weeks before you start treatment with Soliris, your doctor will administer a vaccine against meningococcal infection if it was not previously administered or if your vaccination is outdated.
There were fewer thrombotic events with Soliris treatment than during the same period of time prior to treatment. .
In PNH patients, uncontrolled terminal complement activation andthe resulting complement-mediated intravascular haemolysis are blocked with Soliris treatment.
In aHUS clinical studies, 61 patients(21 paediatric patients)discontinued Soliris treatment with a median follow-up period of 24 weeks.
Patients who entered NMOSD clinical trials while receiving background immunosuppressant therapy continued treatment with immunosuppressant therapy while on Soliris treatment(See section 5.3).