Esimerkkejä Treatment interruption käytöstä Englanti ja niiden käännökset Suomi
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The majority of events resolved after treatment interruption.
Treatment interruption Treatment with MIRCERA is normally long-term.
When you re-start Terapress after any treatment interruption.
Dose Reduction, treatment interruption and treatment discontinuation.
When you re-start Terapress after any treatment interruption.
Treatment interruptions of up to 4 weeks were allowed based on individual tolerability.
Hypothyroidism may be managed with replacement therapy without treatment interruption.
Treatment interruptions of up to 3 weeks were allowed based on individual tolerability.
Adverse reactions, including nephrolithiasis,may lead to treatment interruption.
Skin reactions are very common and treatment interruption or discontinuation may be required.
Adverse reactions, including nephrolithiasis,may lead to treatment interruption.
Treatment interruption should be considered in patients who develop signs or symptoms of acute myocardial ischaemia.
Nd occurrence ofany grade 2 or 3 AE or persistence after treatment interruption.
Most patients recovered from diarrhoea following treatment interruption, anti-diarrhoeal therapy and nintedanib dose reduction.
These serum creatinine elevations generally resolved,most without treatment interruption.
Serous retinopathy can be managed with treatment interruption, dose reduction or with treatment discontinuation see Table 1 in section 4.2.
Zometa treatment should be resumed at the same dose as that prior to treatment interruption.
Laboratory abnormalities should be managed with dose reduction, treatment interruption or with treatment discontinuation see sections 4.2 and 4.8.
Zoledronic acid Teva treatment should be resumed at the same dose as that given prior to treatment interruption.
The management of adverse reactions may require dose reduction, treatment interruption or treatment discontinuation see Tables 1 and 2.
Zoledronic acid Actavis treatment should be resumed at the same dose as that given prior to treatment interruption.
Decrease in LVEF from baseline can be managed using treatment interruption, dose reduction or with treatment discontinuation see section 4.2.
Severe gastrointestinal haemorrhage occurred in 4% of patients andgenerally required treatment interruptions and transfusions.
Haematological adverse reactions Dose reduction or treatment interruption for severe neutropenia and thrombocytopenia are 4 recommended as indicated in the table below.
The most frequent adverse reaction reported for Gilenya 0.5 mg leading to treatment interruption was ALT elevations 2.2.
After treatment interruption and recovery to grade 1 or baseline, dose reduction from 200 mg twice daily to 150 mg twice daily and.
In ivacaftor-treated patients, most transaminase elevations up to 5 x ULN resolved without treatment interruption.
After treatment interruption and recovery of transaminase-values to≤ 2.5 x ULN in conjunction with bilirubin to normal, dose reduction from 200 mg twice daily to 150 mg twice daily and- if a 2nd dose reduction is considered necessary- from 150 mg twice daily to 100 mg twice daily.
In patients with an ejection fraction below the institution's lower limit of normal, cardiac consultation as well as treatment interruption or discontinuation should be considered.
Regarding its safety, although more side effects were reported in patients treated with Vargatef plus docetaxel than in those treated with docetaxel alone, the side effects were considered manageable with dose reductions,supportive treatments and treatment interruptions.