The Yellow Card Scheme is vital in helping the Medicines and Healthcare products Regulatory Agency (MHRA) monitor the safety of all healthcare products in the UK to ensure they are acceptably safe for patients and users.
Reports can be made for:
- suspected adverse drug reactions (ADRs) to all medicines including:
- blood factors and immunoglobulins
- herbal medicines
- homeopathic remedies
- all medical devices available on the UK market
- defective medicines (those that are not of an acceptable quality)
- fake or counterfeit medicines or medical devices
- nicotine-containing electronic cigarettes and refill containers (e-liquids)
It is important that problems with medicines and medical devices and other nicotine e-cigarette products are reported, as the reports help identify new problems with these products.
MHRA will review the product and if necessary and take action to minimise risk and maximise benefit to patients and the public.
MHRA is also able to investigate counterfeit medicines or devices and if necessary take action.
More information HERE