Examples of using Combination with melphalan in English and their translations into Dutch
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Table 1: Starting doses for thalidomide in combination with melphalan and prednisone.
When used in combination with melphalan and prednisone, Velcade is given twice a week on weeks 1, 2, 4 and 5 of a six-week treatment cycle.
Frequency of adverse reactions with thalidomide in combination with melphalan and prednisone.
Lenalidomide in combination with melphalan and prednisone followed by maintenance monotherapy in patients who are not eligible for transplant.
Table 2: Recommended posology for Bortezomib Accord in combination with melphalan and prednisone.
Recommended posology for VELCADE in combination with melphalan and prednisone for patients with previously untreated multiple myeloma Twice weekly VELCADE cycles 1-4.
Table 3: Frequency of adverse drug reactions(ADRs) with thalidomide in combination with melphalan and prednisone.
Thalidomide Celgene in combination with melphalan and prednisone as first line treatment of patients with untreated multiple myeloma,
Table 3: Posology modifications during subsequent cycles of VELCADE therapy in combination with melphalan and prednisone.
VELCADE in combination with melphalan and prednisone is indicated for the treatment of patients with previously untreated multiple myeloma who are not eligible for high-dose chemotherapy with bone marrow transplant.
Newly diagnosed multiple myeloma in patients treated with lenalidomide in combination with melphalan and prednisone.
VELCADE in combination with melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for high-dose chemotherapy with haematopoietic stem cell transplantation.
Dose adjustments for combination therapy Dose modification and re-initiation of therapy when VELCADE is administered in combination with melphalan and prednisone.
Among invasive SPMs, cases of MDS/AML were observed in patients receiving lenalidomide in combination with melphalan or immediately following high dose melphalan
Overall, the safety profile of patients treated with VELCADE in monotherapy was similar to that observed in patients treated with VELCADE in combination with melphalan and prednisone.
Venous thromboembolism was seen to a lesser extent with lenalidomide in combination with melphalan and prednisone in newly diagnosed multiple myeloma
No dose adjustment is proposed for patients older than 75 years who are treated with lenalidomide in combination with melphalan and prednisone.
The most commonly observed adverse reactions associated with the use of thalidomide in combination with melphalan and prednisone are:
Treatment emergent drug-related adverse reactions reported in≥ 10% of patients treated with VELCADE in combination with melphalan and prednisone Vc+M+P M+P.
A 2.12-fold increase in incidence rate of solid tumour SPM has been observed in patients receiving lenalidomide(9 cycles) in combination with melphalan and prednisone(1.57 per 100 person-years)
The benefit achieved with thalidomide and the risk of AML and MDS must be taken into account before initiating treatment with thalidomide in combination with melphalan and prednisone.
Venous thromboembolism was seen to a lesser extent with lenalidomide in combination with melphalan and prednisone in newly diagnosed multiple myeloma.
This increase was not observed in clinical trials of newly diagnosed multiple myeloma in patients taking lenalidomide in combination with low dose dexamethasone compared to thalidomide in combination with melphalan and prednisone.
each cycle lasting 6 weeks, in combination with melphalan and prednisone which are taken on days 1 to 4 of each 6 week cycle.
was not increased as compared to thalidomide in combination with melphalan and prednisone 0.79 per 100 person-years.
25,000/μl or in combination with melphalan and prednisone when the platelet count is≤ 30,000/μl see section 4.2.
The risk of occurrence of hematologic SPM must be taken into account before initiating treatment with Revlimid either in combination with melphalan or immediately following high-dose melphalan and ASCT.
Cases of AML have been observed in clinical trials of newly diagnosed multiple myeloma in patients taking lenalidomide treatment in combination with melphalan or immediately following high dose melphalan and ASCT see section 4.4.