Provide information
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Provide information to complete your report, including, but not limited to
- Contact information
- Country of occurrence of the event
- Age
- Product Name and Dosing Information
- Batch/Lot Number
- Date you experienced the side effect or quality concern
- Description of the side effect or quality concern
- For quality concerns, if the medical device is in your possession (please retain it for 21 days)
Post submission information
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Once successfully submitted, you will receive a confirmation, which lets you know that we have received your information.
Due to high volumes, it may take some time for us to evaluate each report. Please note that we will only reach out to you if we need any further information. If we have all needed information, you will not be contacted by us.
Please do not call to follow up on your submission; this will not speed up the process and may delay our ability to process your submission efficiently. If you have a new side effect or quality concern, please submit a new report.