Shockwave Therapy vs Yellow Card

For users of Extracorporal Shockwave Therapy machines, this app provides detailed treatment instructions (focussed ESWT) for 10 common conditions, plus energy data, contraindications and the ability to keep energy level data and treatment notes for your most common conditions. Conditions covered are Achillodynia, Calcific tendonitis, Golfers Elbow, Patellar tendonitis, plantar fasciitis, pseudoarthrosis, tennis elbow, tibial stress syndrome, trigger points and trochanteric tendonitis. General guidelines and contraindications are also covered. This app features a 3D view of the body, plus individual treatment guidelines with clear images for PiezoWave ESWT treatments. A great way to educate patients and support this powerful therapy!

Use the Yellow Card app to report suspected safety concerns involving healthcare products, including a side effect with a medicine or an adverse medical device incident. The Yellow Card scheme is the UK system run by the MHRA* for collecting and monitoring information on suspected adverse reactions to all medicines including vaccines, blood factors and immunoglobulins, herbal medicines and homeopathic remedies, and all medical devices available on the UK market. The Yellow Card app allows users to: Report safety concerns about: > Suspected side effects to a medicine or vaccine (including herbal products and homeopathic remedies) > Adverse incidents involving a medical device (including software, apps and artificial intelligence) > Suspected defective medicines (a product that is not working properly or not to the manufacturer’s specifications) > Fake and/or unauthorised medicines > Blood products Create an account: > View previously submitted reports > Update your reports > Create a watchlist for alerts to products of interest > Track new safety information published by the MHRA > View numbers of reports received by the MHRA All reports received through the app or website can help the MHRA identify potential new concerns about a medicine, vaccine or medical device and act as an early warning for further investigation. The MHRA will review the product if necessary, and take action to minimise risk and maximise benefit to the patients. *The Medicines and Healthcare products Regulatory Agency (MHRA) is an executive Agency of the Department of Health and Social Care; the MHRA protects and promotes public health and patient safety by ensuring that medicines, healthcare products and medical equipment are used safely and meet appropriate standards of safety, quality, performance and effectiveness.