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Questions were related to service provision at the day of collection; information on stock-outs and numbers of CD4 tests were collected for the 3 months (quarter) prior to the interview date.
Data on patient demographics, vital signs at presentation, medical history, and results of laboratory tests were collected for these patients.
Data on patient demographics, vital signs and physical examination at presentation, medical history, and results of laboratory tests were collected for these samples.
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Blood for cELISA tests were collected from these pigs when they were about 100 kg.
Adverse events (AEs) were recorded at every study visit; routine blood tests were collected periodically for safety evaluation.
Two sets of nasal/throat swabs for influenza testing were collected from each patient.
Blood samples for HIV testing were collected from each patient.
Blood samples for laboratory tests were collected after an overnight fast.
Data retrieved from primary literature: Primary literature was evaluated for test results from diverse in vitro assays (Table 8); 1155 test results were collected for 744 substances (data tables with references are provided in Additional file 1).
Data on clinical status indicators and laboratory test results were collected for one year prior to baseline.
Consultation and chlamydia testing data were collected for two time periods: 12 months prior to and 6 months of the intervention.
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