Adverse Event Reporting Mitozz™

Last updated: November 12, 2025

We take product safety seriously. If you experience an adverse event (any negative health-related event associated with using a dietary supplement) or a serious adverse event (see definitions below), please follow the steps on this page. U.S. law requires the manufacturer, packer, or distributor named on the product label to submit serious adverse events to FDA generally within 15 business days of receiving the report.

1. For Emergencies

If you or someone else is in immediate danger, call 911. For poison emergencies or advice, contact the Poison Help line at 1-800-222-1222. You may also report directly to FDA’s MedWatch program.

2. How to Report to Mitozz™

Provide as much detail as possible via one of these channels:

Include

  • Your contact info; patient age/sex; healthcare provider contact (if any)
  • Product name, lot/expiration, dose, start/stop dates
  • Description of the event, onset date/time, symptoms, diagnosis, test results, hospital/ER visits, and outcome
  • Concomitant products/medicines and relevant medical history

3. Definitions

A serious adverse event is one that results in death, a life-threatening experience, inpatient hospitalization, a persistent or significant disability/incapacity, a congenital anomaly/birth defect, or requires medical/surgical intervention to prevent one of those outcomes.

4. What We Do With Your Report

  • We document all adverse events and maintain records for six (6) years.
  • If your report meets the definition of a serious adverse event associated with our product used in the U.S., we will submit it to FDA using MedWatch (electronically where available or using FDA Form 3500A) no later than 15 business days from receipt, and we will submit any related new medical information received within one year within 15 business days.

5. Reporting Directly to FDA

Consumers and healthcare professionals may report directly to FDA via MedWatch online or by using FDA Form 3500 (voluntary).

6. Privacy

We use your information solely to investigate and fulfil our safety and legal obligations and handle it per our Privacy Policy. We may share necessary details with the FDA and, where applicable, healthcare providers involved in the case.

7. Contact

Nutripharma Technologies LLC
117 NE 1st Avenue, 9th Floor #1032
Miami, FL 33132. 
Email: info@nutripharmatechnologies.com
Phone: 1-786-600-4212