Ascites is found among people who take Inspra, especially for people who are male, 60+ old , have been taking the drug for < 1 month, also take medication Metoprolol Succinate, and have Cardiac failure congestive . We study 1,046 people who have side effects while taking Inspra from FDA and social media. Among them, 6 have Ascites. Find out below who they are, when they have Ascites 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 >>>
Inspra has active ingredients of eplerenone. It is often used in cardiac failure. (latest outcomes from Inspra 1,064 users)
Ascites (accumulation of fluid in the abdominal cavity) has been reported by people with fever, renal failure acute, hepatic failure, diarrhea, hepatic neoplasm malignant (latest reports from 16,737 Ascites patients).
On Jul, 23, 2016
1,046 people reported to have side effects when taking Inspra.
Among them, 6 people (0.57%) have Ascites
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
I got serious fluid buildup while on Sprycel, and while it was less on Tasigna, it still was an occasional issue. I discontinued the tasigna last year, and have been more or less in remission for 14 months. The ascites has, however, returned again. Is anyone else experiencing this problem? I ...
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.