Welcome to the adverse event report page

Adverse drug event (ADE) refers to the adverse medical condition or deterioration of the original medical condition of the patient or clinical trial subject after medication, regardless of whether the event has a causal relationship with the suspected medication. Adverse drug reaction (ADR) refers to the harmful and unexpected response 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 is a quality problem in the product, but the drug manufacturer has the responsibility to collect the adverse events in the use of the product, so as to further evaluate the product characteristics and ensure the safety of public medication.

If you have an adverse event or feel you may be experiencing an adverse event, you should seek advice from a healthcare expert in a timely manner.

If you encounter adverse events when using Jiabo products, please download and fill in the ADR report form or write a descriptive text containing four elements and send it to the following email address, or contact directly by telephone.

上市许可持有人药品不良反应报告表 (1).docx

Tel: 0763-3299010

Email: jbblfy@jiabopharm.com