cH8/1N1 LAIV

Solicited adverse events were assessed by study staff for 60 minutes after each vaccination and and then by study participants daily for 7 days on a a diary card. Solicited local reactions included: * Post LAIV dose: nasal congestion, rhinorrhea; * Post IIV dose: pain, redness, swelling.

Solicited adverse events were assessed by study staff for 60 minutes after each vaccination and and then by study participants daily for 7 days on a a diary card. Solicited general reactions included: * abdominal pain * arthralgia * cough * diarrhea * fatigue * fever * headache * myalgia * nausea * shivering * sore throat * vomiting * wheezing

Unsolicited adverse events (AEs) are any AEs reported spontaneously by the participant, observed by the study personnel during study visits or those identified during review of medical records or source documents, such as diary cards. Participants were asked to record any unsolicited symptoms or other illness description in their diary card during the 28 days after each vaccination. All AEs, including clinical laboratory test results, were assessed by a study clinician and the study subject (as applicable) to quantify severity using a protocol-defined grading system as mild (mild symptoms, easily tolerated, not interfering with daily activities), moderate (causing some interference with daily activity), or severe (severe symptoms that prevent normal every day activities). The investigator assessed the relationship between study vaccines and the occurrence of each AE using clinical judgment.

Hematological and biochemical parameters assessed included hemoglobin, platelets, red blood cells, white blood cells (WBC), absolute neutrophil count (ANC), lymphocytes, monocytes, eosinophils, basophils, alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatinine, blood urea nitrogen (BUN) and BUN-to-creatinine ratio. Grading of laboratory parameters was based on the FDA Guidance for Industry: Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled in Preventive Vaccine Clinical Trials as Grade 1 (Mild), Grade 2 (Moderate), Grade 3 (severe), or Grade 4 (Potentially life-threatening). Grade 2 or higher: * BUN: \> 26 mg/dL * Creatinine: \> 1.7 mg/dL * ALT, AST: \> 2.5 × upper limit of normal (ULN) * Hemoglobin: \< 11.0 g/dL (females) or \< 12.5 g/dL (males) or change from baseline \> 1.5 g/dL * WBC: \> 15,000 cell/mm³ or \< 2,500 cell/mm³ * Lymphocytes: \< 750 cell/mm³ * ANC: \< 1,500 cell/mm³ * Eosinophils: \> 1,500 cell/mm³ * Platelets: \< 125,000 cell/mm³

An MAE is an event for which the participant received medical attention such as hospitalization, an emergency room visit, or a visit to or from medical personnel. pIMDs are a subset of AEs that include autoimmune diseases and other inflammatory and/or neurologic disorders of interest which may or may not have an autoimmune etiology. LC-ILI is defined as at least 1 systemic symptom (fever or myalgia) AND at least 1 respiratory symptom (cough or sore throat), confirmed by polymerase chain reaction (PCR) assay. An SAE is an AE that met any of the following: * Death * Life threatening * Required inpatient hospitalization or prolongation of existing hospitalization * Results in persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions * Results in congenital anomaly/birth defect * An important medical event that may jeopardize the well-being of the subject or require medical or surgical intervention to prevent an above outcome.