Skip to main content
. 2000 May;44(5):1276–1283. doi: 10.1128/aac.44.5.1276-1283.2000

TABLE 3.

Four-week daily oral administration of ICN 17261 does not induce anemia or leukopenia in rats

Groupa Test material Dose (mg/ml/day)b Level of:
Hemoglobinc
Hematocritd
Leukocytee
Lymphocytef
Day 11 Day 30 Day 60 Day 11 Day 30 Day 60 Day 11 Day 30 Day 60 Day 11 Day 30 Day 60
1 Control 0 14.1 ± 0.66 14.4 ± 0.61 15.1 ± 0.64 41.4 ± 2.08 42.6 ± 1.76 44.2 ± 1.78 7.5 ± 1.86 8.4 ± 2.65 11.8 ± 2.52 6.5 ± 1.73 7.1 ± 2.51 10.3 ± 2.64
2 ICN 17261 60–300 13.9 ± 0.63 14.4 ± 0.56 15.4 ± 0.37 40.7 ± 2.13 42.4 ± 1.26 45.1 ± 1.1 7.2 ± 0.83 9.0 ± 1.55 10.9 ± 1.26 6.1 ± 0.79 7.4 ± 1.26 9.0 ± 1.18
3 ICN 17261 180 14.0 ± 0.61 14.6 ± 0.54 15.5 ± 0.75 40.9 ± 2.01 42.9 ± 1.52 45.5 ± 2.97 6.8 ± 1.57 8.4 ± 1.88 9.6 ± 2.98 5.8 ± 1.31 6.8 ± 1.89 7.8 ± 2.81
4 Ribavirin 180 12.1 ± 1.01g 11.7 ± 1.54g 15.9 ± 0.45 32.9 ± 4.05g 31.7 ± 5.96g 45.3 ± 0.62 5.4 ± 1.41g 3.8 ± 1.10g 8.2 ± 2.79 4.8 ± 1.37g 2.8 ± 0.94g 6.8 ± 2.52
a

Measurements at days 11 and 30 were from 12 male rats from each group except for group 4 (15 rats). Day 60 measurements were from four animals from each group designated as recovery animals which were dosed daily for 29 days, after which dosing was discontinued, and the animals were observed for reversibility, persistence, or delayed occurrence of toxic effects for 31 days posttreatment. 

b

Dose regimen as in Table 1

c

Hemoglobin values are shown as grams per deciliter. 

d

Hematocrit values are shown as percentage of blood volume. 

e

Leukocyte count shown as cells × 10−3/μl. 

f

Lymphocyte count shown as cells × 10−3/μl. 

g

Group mean is significantly (P ≤ 0.05) different from mean of control group 1.