Suspected adverse reactions and product quality problems can be reported to SAHPRA, usually through the reporting form or app, by patients as well as health professionals. Reporting does not replace clinical care — contact your clinic first if you are unwell — but it contributes to national safety monitoring.
Also known as: side effect reporting, pharmacovigilance, reporting a reaction
Related South Africa guides
Sources
- SAHPRA (South African Health Products Regulatory Authority)
Last reviewed: 8 September 2026. Written by the Antega Editorial Team. General information only — always follow the advice of your own clinic, doctor or pharmacist.
