Adverse Event Reporting Platform
- Time of issue:2019-08-22 00:00:00
Welcome to the adverse event report page
Adverse Drug Event (abbreviated as ADE) refers to the deterioration of the adverse medical condition or the original medical condition after the patient or clinical test subject is treated, regardless of whether the event has a causal relationship with the suspected medication. Adverse Drug Reaction (ADR) refers to the harmful and unanticipated reaction to drugs when the human body uses normal doses to prevent, diagnose, treat or improve physiological functions.
The occurrence of adverse events does not mean that there are quality problems in the products, and the pharmaceutical manufacturers are responsible for collecting the adverse events in the use of the products to further evaluate the product characteristics and ensure the safety of the public.
If you have an adverse event on your body, or if you feel you may be experiencing an adverse event, you should seek advice from a health care professional in a timely manner.
If you encounter an adverse event when using Zhuhai homologous pharmaceutical products, please download and fill out the ADR report form or write a descriptive text containing four elements, send it to the e-mail address specified by the following pharmaceutical manufacturer, or contact us directly.