Pharmacovigilance (PV) is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems.
The Pharmacovigilance System at ACDIMA International aims to ensure patient safety through monitoring the Benefit/Risk ratio of our products currently available in the Egyptian Market.
🛡️ Our commitment to pharmacovigilance reflects our dedication to patient safety — ensuring every product we market meets the highest standards of benefit and minimal risk throughout its lifecycle.
Collecting adverse event reports from healthcare providers and patients
Evaluating causality and severity of reported adverse reactions
Analysing patterns and signals to build a complete safety profile
Taking action to minimise risks and protect patients
If you experience any adverse events concerning any of ACDIMA / Techno Pharma products, please report to us through one of the following channels:
Send your adverse event report directly to our Pharmacovigilance team via email.
qppv@acdimatrading.comUse our online reporting forms — available in both English and Arabic.
English Form → Arabic Form (عربي) →Choose your preferred language to fill out the adverse event reporting form. Your report helps us ensure the safety of all patients.
Report an adverse event in English. The form covers all required information for a complete pharmacovigilance report.
📋 Open English Formأبلغ عن حدث ضائر باللغة العربية. يغطي النموذج جميع المعلومات المطلوبة لتقرير اليقظة الدوائية.
📋 فتح النموذج العربيOur dedicated Pharmacovigilance team is available to assist healthcare professionals and patients with any drug safety concerns or adverse event reports.