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When reporting an adverse experience, please be sure to include information about: The affected person (whether a user or nonuser) Manufacturer name Brand name, model, and serial number of the product, device, or e-liquid, as applicable Where the tobacco product(s) were purchased Whether the tobacco product(s) were modified in any way or whether there was a device malfunction Use of or exposure to other tobacco products, medications, supplements, substances of abuse or toxins around the same time Any other symptoms or warnings before the adverse experience, such as nausea, vomiting, change in the users behavior, alertness, vision or hearing Details about the pattern of product use or exposure before the event (duration, amount and intensity of product use) as well as the time between the latest use and the adverse experience Health effects details: Specific areas of the body affected, symptom progression, how long symptoms lasted, course of recovery, and any medical testing, care and treatment decisions rendered Underlying health conditions, health history and family history Whether product use continued or not after the event and whether additional events occurred Whether you reported the event elsewhere, such as to a poison control center, the retailer, or the manufacturer You can also upload relevant medical records, photos, or other files that include or supplement this information