Examples of using Dose modifications in English and their translations into Slovak
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Dose modifications.
Recommended trametinib dose modifications.
Dose Modifications for Toxicities.
Table 5 Recommended dose modifications for neutropenia.
Dose modifications for renal toxicities.
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In subjects with asthma and subjects with COPD there are no recommended dose modifications.
Dose modifications* and management recommendations.
For cisplatin and 5-fluorouracil dose modifications, see the corresponding summary of product characteristics.
Dose modifications for haematologic toxicities.
For cisplatin and 5-fluorouracil dose modifications, see the corresponding summary of product characteristics.
Dose modifications based on body weight are not required.
Table 4 Recommended dose modifications for gastrointestinal toxicity.
The dose modifications should be considered(see section 4.2).
Dose modifications for left ventricular dysfunction.
Table 5 Dose modifications for left ventricular dysfunction.
Dose modifications are to be applied in 40 mg(one tablet) steps.
Following dose modifications, the cycle duration should return to 28 days.
For dose modifications for thrombocytopenia, see sections 4.2 and 4.4.
Table 2 Dose modifications from recommended lenvatinib daily dosea.
Dose modifications due to haematological toxicity in subsequent cycles.
Dose modifications for hematologic toxicity on days 8 and 15 of any cycle.
Dose modifications due to peripheral neuropathy are described in Table 2.
All dose modifications should be based on the worst preceding toxicity.
Dose modifications for non-haematological toxicities at any time during treatment.
Table 2 Dose modifications from recommended lenvatinib daily dose a.
Dose modifications or interruption for patients developing anaemia may also be considered.
Dose modifications depending on duration of dosing interruption due to toxicity.
Dose modifications were required in 30% of patients, most commonly for anaemia and neutropaenia.
Recommended dose modifications for Thalidomide Celgene-related neuropathy in first line treatment of multiple myeloma.
Table 2: Recommended dose modifications for Thalidomide Celgene-related neuropathy in first line treatment of multiple myeloma.
