Examples of using Dose modifications in English and their translations into Romanian
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Dose modifications.
Table 1 Recommended Cotellic dose modifications.
Dose modifications.
Table 1. Recommended dose modifications for TAGRISSO.
Dose modifications for renal toxicities.
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Table 3 Recommended dose modifications for hepatic toxicity.
Dose modifications for haematologic toxicities.
Recommended actions and dose modifications are presented in table 3.
Dose modifications for special populations.
For Grade 1 and2 toxicities there are no dose modifications recommended.
Table 1 Dose modifications for myelosuppression.
In adolescents(12 years or older),there are no recommended dose modifications.
Recommended dose modifications are described below.
Dose modifications during treatment(all indications).
Guidelines for dose modifications are summarised in Table 1.
Dose modifications are to be applied in 40 mg(one tablet) steps.
Table 1- Recommended dose modifications for adverse reaction in patients treated with cabazitaxel.
Dose modifications due to peripheral neuropathy are described in Table 2.
Table 1: Dose modifications for drug induced hepatotoxicity.
Dose modifications were required in 30% of patients, most na.
Following dose modifications, the cycle duration should return to 28 days.
No dose modifications are necessary in elderly patients with normal renal function.
Temsirolimus dose modifications based on weekly ANC and platelet counts.
The dose modifications should be considered(see section 4.2).
For capecitabine dose modifications, see capecitabine summary of product characteristics.
All dose modifications should be based on the worst preceding toxicity.
Table 5 Dose modifications for left ventricular dysfunction.
Dose modifications are not necessary when administered in combination with Genvoya.
Dose modifications of zidovudine in this situation have not been formally evaluated.
Dose modifications for hematologic toxicity on days 8 and 15 of any cycle.