Created at Source Raw Value Validated value
Nov. 16, 2021, 6:30 p.m. usa

known previous exposure to sars-cov-2 or receipt of an investigational product for the prevention or treatment of covid-19, middle east respiratory syndrome (mers), or severe acute respiratory syndrome (sars). is in a current occupation with high risk of exposure to sars-cov-2 individuals with the following underlying medical conditions who are at higher risk (or might be at higher risk) of severe illness from covid-19 per the cdc's guidance donation or use of blood or blood products within 4 weeks prior to vaccination or planned donation during the study period. diagnosed bleeding disorder or significant bruising or bleeding difficulties that could make blood draws problematic. any condition that resulted in the absence or removal of the spleen. positive hiv, hbsag or hcv tests at the screening visit. stool sample with occult blood at screening. use of antiviral medications, including anti-retrovirals, or any prescriptive medications for the prevention of covid-19 within 7 days before vaccination use of antibiotics, proton pump inhibitors, h2 blockers or antacids or medications known to affect the immune function within 7 to 14 days before vaccination regular use of nonsteroidal anti-inflammatory drugs, sulfonylureas, and angiotensin ii blockers within 7 days before vaccination acute disease within 72 hours prior to vaccination defined as the presence of a moderate or severe illness history of drug, alcohol or chemical abuse within 1 year of screening or positive urine drug screen for drugs of abuse at screening history of hypersensitivity or allergic reaction to any component of the investigational vaccine administration of any investigational vaccine, drug or device within 8 weeks preceding vaccination any other condition that in the clinical judgment of the investigator would jeopardize the safety or rights of a subject participating in the trial, would render the subject unable to comply with the protocol or would interfere with the evaluation of the study endpoints.

known previous exposure to sars-cov-2 or receipt of an investigational product for the prevention or treatment of covid-19, middle east respiratory syndrome (mers), or severe acute respiratory syndrome (sars). is in a current occupation with high risk of exposure to sars-cov-2 individuals with the following underlying medical conditions who are at higher risk (or might be at higher risk) of severe illness from covid-19 per the cdc's guidance donation or use of blood or blood products within 4 weeks prior to vaccination or planned donation during the study period. diagnosed bleeding disorder or significant bruising or bleeding difficulties that could make blood draws problematic. any condition that resulted in the absence or removal of the spleen. positive hiv, hbsag or hcv tests at the screening visit. stool sample with occult blood at screening. use of antiviral medications, including anti-retrovirals, or any prescriptive medications for the prevention of covid-19 within 7 days before vaccination use of antibiotics, proton pump inhibitors, h2 blockers or antacids or medications known to affect the immune function within 7 to 14 days before vaccination regular use of nonsteroidal anti-inflammatory drugs, sulfonylureas, and angiotensin ii blockers within 7 days before vaccination acute disease within 72 hours prior to vaccination defined as the presence of a moderate or severe illness history of drug, alcohol or chemical abuse within 1 year of screening or positive urine drug screen for drugs of abuse at screening history of hypersensitivity or allergic reaction to any component of the investigational vaccine administration of any investigational vaccine, drug or device within 8 weeks preceding vaccination any other condition that in the clinical judgment of the investigator would jeopardize the safety or rights of a subject participating in the trial, would render the subject unable to comply with the protocol or would interfere with the evaluation of the study endpoints.

Oct. 26, 2020, 11:31 p.m. usa

1. known previous exposure to sars-cov-2 or receipt of an investigational product for the prevention or treatment of covid-19, middle east respiratory syndrome (mers), or severe acute respiratory syndrome (sars). 2. is in a current occupation with high risk of exposure to sars-cov-2 3. individuals with the following underlying medical conditions who are at higher risk (or might be at higher risk) of severe illness from covid-19 per the cdc's guidance 4. donation or use of blood or blood products within 4 weeks prior to vaccination or planned donation during the study period. 5. diagnosed bleeding disorder or significant bruising or bleeding difficulties that could make blood draws problematic. 6. any condition that resulted in the absence or removal of the spleen. 7. positive hiv, hbsag or hcv tests at the screening visit. 8. stool sample with occult blood at screening. 9. use of antiviral medications, including anti-retrovirals, or any prescriptive medications for the prevention of covid-19 within 7 days before vaccination 10. use of antibiotics, proton pump inhibitors, h2 blockers or antacids or medications known to affect the immune function within 7 to 14 days before vaccination 11. regular use of nonsteroidal anti-inflammatory drugs, sulfonylureas, and angiotensin ii blockers within 7 days before vaccination 12. acute disease within 72 hours prior to vaccination defined as the presence of a moderate or severe illness 13. history of drug, alcohol or chemical abuse within 1 year of screening or positive urine drug screen for drugs of abuse at screening 14. history of hypersensitivity or allergic reaction to any component of the investigational vaccine 15. administration of any investigational vaccine, drug or device within 8 weeks preceding vaccination 16. any other condition that in the clinical judgment of the investigator would jeopardize the safety or rights of a subject participating in the trial, would render the subject unable to comply with the protocol or would interfere with the evaluation of the study endpoints.

1. known previous exposure to sars-cov-2 or receipt of an investigational product for the prevention or treatment of covid-19, middle east respiratory syndrome (mers), or severe acute respiratory syndrome (sars). 2. is in a current occupation with high risk of exposure to sars-cov-2 3. individuals with the following underlying medical conditions who are at higher risk (or might be at higher risk) of severe illness from covid-19 per the cdc's guidance 4. donation or use of blood or blood products within 4 weeks prior to vaccination or planned donation during the study period. 5. diagnosed bleeding disorder or significant bruising or bleeding difficulties that could make blood draws problematic. 6. any condition that resulted in the absence or removal of the spleen. 7. positive hiv, hbsag or hcv tests at the screening visit. 8. stool sample with occult blood at screening. 9. use of antiviral medications, including anti-retrovirals, or any prescriptive medications for the prevention of covid-19 within 7 days before vaccination 10. use of antibiotics, proton pump inhibitors, h2 blockers or antacids or medications known to affect the immune function within 7 to 14 days before vaccination 11. regular use of nonsteroidal anti-inflammatory drugs, sulfonylureas, and angiotensin ii blockers within 7 days before vaccination 12. acute disease within 72 hours prior to vaccination defined as the presence of a moderate or severe illness 13. history of drug, alcohol or chemical abuse within 1 year of screening or positive urine drug screen for drugs of abuse at screening 14. history of hypersensitivity or allergic reaction to any component of the investigational vaccine 15. administration of any investigational vaccine, drug or device within 8 weeks preceding vaccination 16. any other condition that in the clinical judgment of the investigator would jeopardize the safety or rights of a subject participating in the trial, would render the subject unable to comply with the protocol or would interfere with the evaluation of the study endpoints.