There is no Trigger finger reported by people who take Diovan hct yet. We study 2,148 people who have side effects while taking Diovan hct from FDA and social media. Find out below who they are, when they have Trigger finger 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 >>>
Diovan hct has active ingredients of hydrochlorothiazide; valsartan. It is often used in high blood pressure. (latest outcomes from Diovan hct 2,457 users)
Trigger finger has been reported by people with breathing difficulty, muscle atrophy, speech impairment (adult), heart palpitations, hypersensitivity (latest reports from 1,558 Trigger finger patients).
On Aug, 31, 2016
No report is found.
I suffered a major depressive episode after being given both oral and injected cortisone about 10 years ago. I also gained about 10 pounds in a 2 week period as my appetite was insatiable. I now have a trigger finger and have been advised that the best treatment is a cortisone shot.
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.