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Consequently, the lowest mean total CD34+ cell dose was collected from patients with NHL (1.69 × 10 cells/kglls/kg b.w)., compared with 2.99 × 10 cells/kglls/kg b.w.
21 Patient medication information (eg, initiation and discontinuation dates, frequency, dose) was collected during patient interviews conducted as part of routine clinic encounters.
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Blood samples during the intensive collection phase (up to 12 h after the last dose) were collected through an indwelling intravenous cannula flushed with 0.5 ml heparinized saline solution after each sample collection.
Wound tissue from the mice given the highest antibody dose were collected for histology on day 7, day 10 and day 21 after wounding (3 mice per time-point).
Data on the exact time of administration of the previous dose are collected.
Baseline data, including patient characteristics (age, gender, tumor location, tumor volume, and cochlea size) and treatment of VS (date of radiosurgery and prescribed dose) were collected.
Plasma samples (n = 32) were collected for up to 48 h after the loading dose were collected, with specific emphasis after the first and after the final 5th paracetamol dose (at 24 h).
The drug infusion was continued for 60 min. The hemodynamic (3 min averaged values) and oxygen saturation variables at 30 and 60 min of each infusion dose were collected for analysis.
Costs of uterotonics, oxytocin per ampoule (10 IU) and misoprostol per dose, were collected from hospital pharmacies and hospital administrators in one facility in Zambia and one facility in Zimbabwe.
In the RELAX-AHF phase III study, blood samples, weight, and diuretic dose were collected in all patients at baseline and at 24 h (day 1); 48 h (day 2); on days 3 and 4, if in hospital; and on days 5, 14, and 60 for standard haematology and chemistry at a central laboratory using commercially available, validated assays.
Total urine through 24-hours after the start of flavopiridol dosing was collected from patients enrolled in an IRB-approved phase II protocol NCI-70000).
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