Table 6.
Adverse effects | Children (n = 29) |
|
---|---|---|
n | % | |
Mild neutropeniaa (1001–1499 cells/mm3) | 4 | 13.8 |
Moderate neutropenia b (501–1000 cells/mm3) | 7 | 24.1 |
Severe neutropeniac (≤500 cells/mm3) | 2 | 6.9 |
Mild megaloblastic anemia (Hemoglobin: 10.1–11.9 g/dL) | 1 | 3.5 |
Moderate megaloblastic anemia (Hemoglobin: 8.1–10.0 g/dL) | 0 | 0.0 |
Severe megaloblastic anemiac (Hemoglobin: ≤8.0 g/dL) | 1 | 3.5 |
Mild thrombocytopeniac (platelets 101,000–140,000/mm3) | 1 | 3.5 |
Moderate thrombocytopeniad (platelets 51,000–100,000/mm3) | 1 | 3.5 |
Severe thrombocytopenia (platelets ≤ 50,000/mm3) | 0 | 0.0 |
Mild hepatitis (AST and/or ALT ≤ two times the reference value) | 3 | 10.3 |
Moderate hepatitis (AST and/or ALT > two times the reference value, and normal protrombine time test) | 1 | 3.5 |
Severe hepatitis (protrombine time test < 50.0% or INR > 1.3) | 0 | 0.0 |
AST, aspartate aminotransferase; ALT, alanine aminotransferase; INR, international normalized ratio.
1 patient received zidovudine (AZT) and ganciclovir concomitantly, 1 patient received ganciclovir concomitantly.
1 patient received zidovudine concomitantly.
1 patient that received zidovudine concomitantly presented severe neutropenia, severe megaloblastic anemia, and mild thrombocytopenia.
1 patient received ganciclovir concomitantly.