There is no Duchenne muscular dystrophy reported by people who take Lithium carbonate yet. We study 2,148 people who have side effects while taking Lithium carbonate from FDA and social media. Find out below who they are, when they have Duchenne muscular dystrophy 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 >>>
Lithium carbonate has active ingredients of lithium carbonate. It is often used in bipolar disorder. (latest outcomes from Lithium carbonate 15,550 users)
Duchenne muscular dystrophy (severe form of muscular dystrophy caused by a genetic defect) has been reported by people with myoglobinuria, abdominal pain, peptic ulcer perforation, cardiac failure congestive (latest reports from 50 Duchenne muscular dystrophy patients).
On Jul, 30, 2016
No report is found.
Hey, I'm Jon! I got diagnosed with Type 1 Bipolar about two months ago. I have been taking Lithium so far, and am looking to pair it with Modafinil to reduce brain fog. I can't wait to hear more about all of your experiences! -Jon
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.