There is no Carpal tunnel decompression reported by people who take Sudafed 12 hour yet. We study 2,148 people who have side effects while taking Sudafed 12 hour from FDA and social media. Find out below who they are, when they have Carpal tunnel decompression and more.
On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>
Sudafed 12 hour has active ingredients of pseudoephedrine hydrochloride. It is often used in nasal congestion. (latest outcomes from Sudafed 12 hour 4,042 users)
Carpal tunnel decompression has been reported by people with osteoporosis, rheumatoid arthritis, osteopenia, type 2 diabetes, high blood pressure (latest reports from 632 Carpal tunnel decompression patients).
On Oct, 26, 2016
No report is found.
Whenever I try to take the calcium/vit. D supplement as prescribed, I get severe epigastric pain to the point that I am unable to eat anything and actually have a hard time even drinking as well. I will take it for 2 days before I can't stand it and then remain I'll for about 4 more days. I have ...
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.