Write-up: Initial and non-serious report received from the patient''s parent (a healthcare professional) on 20 August 2007. A 14-year-old female with no pre-existing medical conditions or allergies received subcutaneous injections of Menactra (lot number and site not reported) and Varicella (manufacturer, Lot number and site not reported) on 17 August 2007 and that same day she experienced pain and redness at the injection site. The following day, the injection site was very swollen (9x6 inches), indurated, edematous and itchy, with no drainage. The patient was afebrile. It was reported that the patient was to see a doctor. Recovery status had been reported as "not recovered". The patient was previously vaccinated with Gardasil (manufactured by Merck); Lot number and route/site not reported) on 18 July 2007. No additional information had been provided at the time of this report.