The platelets were decreased, serum liver enzymes were increased and leucopenia was seen.
2
Six patients required discontinuation of medication, two because of leucopenia.
3
In association with the leucopenia and the oropharyngeal lesions, a variety of other infective processes were seen.
4
Investigations showed that that the patient had leucopenia, positive antinuclear and anti-double-stranded DNA antibodies and lupus nephritis.
5
This regimen was associated with severe hematological toxicity, mainly leucopenia; five toxic deaths related to sepsis were observed.
6
Grade 3 leucopenia occurred in 1 cycle and one case of neutropenic fever.
7
Severe staphylococcal pneumonia with shock, leucopenia, hemoptysia and high mortality rate have been previously described in children and young adults.
8
However, obtaining blood through phlebotomy is often challenging in patients with conditions like severe leucopenia or hemophilia, pediatric and elderly patients.
9
Toxicity was almost absent in arm A and moderate in arm B, represented mainly by haematological toxicity (usually leucopenia).
10
There were no grade 3 or 4 subacute toxicities of anemia, leucopenia, genitourinary or gastrointestinal effects.
11
One grade 3 of acute toxicity for diarrhea, thrombocytopenia and three grade 3 leucopenia were noted during CCRT.
12
Of 150 cycles administered, we observed 10 cases of Grade 3 leucopenia and 4 cases of Grade 4 leucopenia.
13
The most commonly observed toxicities were grade 1-2 leucopenia, alopecia, nausea and vomiting; no grade 3-4 toxicities were observed.
14
Leucopenia was less severe.
15
Leucopenia was observed after treatment at 18.30 hr.
16
Leucopenia and lymphopenia were the most common signs of infection while liver and kidney damage were rare but may cause bad outcomes for patients.