If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.
Scandishake Side Effects Reported to FDA
Scandishake Side Effect Report#9146582 Cardiac Disorder
This is a report of a 87-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: medical diet, who was treated with Scandishake (dosage: NA, start time: 2012), combined with: NA. and developed a serious reaction and side effect(s): Cardiac Disorder after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Scandishake treatment in female patients, resulting in Cardiac Disorder side effect.
Scandishake Side Effect Report#9095173 Cerebral Atrophy, Multiple System Atrophy, Dysphagia
This report suggests a potential ScandishakeCerebral Atrophy side effect(s) that can have serious consequences. A 76-year-old male patient (weight: NA) from US was diagnosed with the following symptoms/conditions: medical diet and used Scandishake (dosage: NA) starting NS. After starting Scandishake the patient began experiencing various side effects, including: Cerebral Atrophy, Multiple System Atrophy, DysphagiaAdditional drugs used concurrently: NA. Although Scandishake demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Cerebral Atrophy, may still occur.
The appearance of Scandishake on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.
What are common Scandishake Side Effects for Women?
It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.
Why Your Notes are Important
Your notes could be helpful in several ways:
You can use them to remind you of details that may alert your health care professional(s) to a problem
You will have a record to refer to in the future, in case you are ever prescribed the same medicine again
You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.
Medicine Name and Dosage:
Date & Time
Other Medicine(s) or Treatment(s)
Scale: 1 = very mild to 10 = very bad
Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Scandishake reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.