Product Safety
Report An ADR
Our unwavering focus is on the well-being and safety of our patients. Aware that unexpected issues may occur, we deeply appreciate the confidence you have in our products. By swiftly resolving any adverse events and quality issues, we reaffirm our commitment to openness, safety, regulatory compliance, and customer satisfaction.
How to Report an ADR
01
Fill Out CIOMS Form
Please find our CIOMS form below. Fill in all required spaces with all the necessary information required.
02
Send
Email
Email us at medixcare@trumholdings.co.bw; cc medixregulatory@trumholdings.co.bw with your name, any necessary information, and your filled-out CIOMS Form. All information is sent directly to MedixCare.
03
Call Our
Line
Feel free to call us on our 24-hour Mobile Numbers: 71 217 408 / 75 854 941, with any queries. Our trained experts will guide you through the reporting process.
After Submitting a Report
Once a report is submitted, all adverse events and quality complaints are meticulously documented, with strict monitoring of reporting timelines to ensure timely feedback. Our pharmacists are thoroughly trained to identify and process adverse events and product quality issues. They collect relevant data, accurately document each case, and promptly report safety information to the manufacturers or their partners’ pharmacovigilance departments.