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Fig 1.

Study subject disposition.

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Table 1.

Demographic and baseline clinical features of study subjects.

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Table 2.

Baseline haematological and biochemical values of study subject.

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Fig 2.

Increase in the mean (± s.e.m) platelet counts during course of treatment in the treatment group (black) and Placebo group (grey) subjects.

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Fig 3.

Mean (± s.e.m) percent increase in platelet count post treatment (day 3) in treatment group (black) and placebo group (grey) subjects.

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Fig 4.

Mean (± s.e.m) percentage increase in platelet count post treatment (day 3) in treatment group (black) and placebo group (grey) subjects in the febrile, critical and recovery phases of dengue illness.

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Fig 5.

Mean (± s.e.m) percentage increase in platelet count post treatment (day 3) in treatment group (black) and placebo group (grey) subjects with primary and secondary dengue infection.

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Fig 6.

Mean (± s.e.m) percentage increase in platelet count post treatment (day 3) in treatment group (black) and placebo group (grey) in the NS1 (+) and NS (-) subgroup of study subjects.

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Fig 7.

Kaplan-Meier estimates of probability of platelet count of ≤ 50000 per μL by day 6 in treatment group (black) and placebo group (grey).

HR denotes hazard ratio.

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Fig 8.

Increase in the mean (± s.e.m) hematocrit values during course of treatment in the treatment group (black) and placebo group (grey) subjects.

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Fig 9.

Mean (± s.e.m) percent decrease in HCT value (%) post treatment (day 3) in treatment group (black) and placebo group (grey) subjects.

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Table 3.

Days of hospitalization of patients in treatment and placebo group.

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Table 4.

Platelet transfusion details of study subjects in treatment and placebo groups.

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Fig 10.

Mean percentage (±s.e.m) changes in plasma cytokine levels by 72 hrs (day 3) in the treatment group (black) and placebo group (grey) (a) IFN-γ (b) TNF-α (c) IL-6 (d) IL-4.

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Table 5.

Mean (±se.m) plasma levels of cytokines measured on day 0 (pre-treatment) and day 3 (post-treatment) in study subjects (n = 20).

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Fig 11.

Mean (± s.e.m) percentage decrease in plasma viral NS1 titers by day 3 in treatment group (black) and placebo group (grey) subjects.

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