{"description":"Number of subjects at risk included randomized subjects who had follow-up. For Group 4 (Extension), number of subjects at risk included those who received \\>=1 vaccination in the extension study. Both serious and Other AEs were collected in the base period and only serious AEs were collected in the extension period.","eventGroups":[{"description":"The Vaccination Period for the base study encompassed Day 1 through Month 7, during which time study subjects in Group 1 were vaccinated (at Day 1, Month 2 and Month 6) with the Quadrivalent HPV vaccine.\n\nThe Follow-up Period for the Base Study encompassed the follow-up of subjects who had received the Quadrivalent HPV vaccine; from completion of the Vaccination Period at Month 7 through Month 48 of the study.","id":"EG000","otherNumAffected":2458,"otherNumAtRisk":2673,"seriousNumAffected":50,"seriousNumAtRisk":2673,"title":"Group 1 - Base Study Quadrivalent Human Papillomavirus Vaccine"},{"description":"The Vaccination Period for the base study encompassed Day 1 through Month 7, during which time study subjects in Group 2 were vaccinated (at Day 1, Month 2 and Month 6) with the Monovalent (HPV 16) HPV vaccine.\n\nThe Follow-up Period for the Base Study encompassed the follow-up of subjects who had received the Monovalent (HPV 16) HPV vaccine; from completion of the Vaccination Period at Month 7 through Month 48 of the study.","id":"EG001","otherNumAffected":276,"otherNumAtRisk":299,"seriousNumAffected":4,"seriousNumAtRisk":299,"title":"Group 2 - Base Study Monovalent HPV (Type 16) Vaccine"},{"description":"The Vaccination Period for the base study encompassed Day 1 through Month 7, during which time study subjects in Group 3 were vaccinated (at Day 1, Month 2 and Month 6) with placebo.\n\nThe Follow-up Period for the Base Study encompassed the follow-up of subjects who had received placebo; from completion of the Vaccination Period at Month 7 through Month 48 of the study.","id":"EG002","otherNumAffected":2331,"otherNumAtRisk":2672,"seriousNumAffected":45,"seriousNumAtRisk":2672,"title":"Group 3 - Base Study Placebo"},{"description":"This group includes subjects who entered the extension including subjects who in the base study received fewer than the full three doses of Quadrivalent HPV vaccine during the base study (i.e., subjects who received placebo in the base study; subjects who received monovalent \\[type 16\\] HPV vaccine in the base study, or subjects who received \\<=2 doses of quadrivalent HPV vaccine in the base study). Subjects who discontinued the base portion of the study could enter the extension portion of the study. In the extension period subjects designated as \"Completed Period\" are those who received three doses of quadrivalent HPV vaccine and completed all required follow-up visits. Subjects designated as \"Not Completed\" are those who: a) Received all three vaccinations, but did not complete follow-up; b) Did not receive all vaccinations, but completed follow-up, or c) Did not receive all vaccinations, and did not complete follow-up.","id":"EG003","otherNumAffected":0,"otherNumAtRisk":0,"seriousNumAffected":5,"seriousNumAtRisk":801,"title":"Group 4 - Quadrivalent Human Papillomavirus Vaccine Extension"}],"frequencyThreshold":"1","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 11.1","stats":[{"groupId":"EG000","numAffected":88,"numAtRisk":2673},{"groupId":"EG001","numAffected":8,"numAtRisk":299},{"groupId":"EG002","numAffected":81,"numAtRisk":2672},{"groupId":"EG003","numAffected":0,"numAtRisk":0}],"term":"Abdominal pain"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 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infection"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Infections and infestations","sourceVocabulary":"MedDRA 11.1","stats":[{"groupId":"EG000","numAffected":10,"numAtRisk":2673},{"groupId":"EG001","numAffected":4,"numAtRisk":299},{"groupId":"EG002","numAffected":16,"numAtRisk":2672},{"groupId":"EG003","numAffected":0,"numAtRisk":0}],"term":"Vulvovaginal candidiasis"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Injury, poisoning and procedural complications","sourceVocabulary":"MedDRA 11.1","stats":[{"groupId":"EG000","numAffected":4,"numAtRisk":2673},{"groupId":"EG001","numAffected":3,"numAtRisk":299},{"groupId":"EG002","numAffected":4,"numAtRisk":2672},{"groupId":"EG003","numAffected":0,"numAtRisk":0}],"term":"Procedural pain"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Musculoskeletal and connective tissue disorders","sourceVocabulary":"MedDRA 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