Creatinine renal clearance increased is reported only by a few people who take Micardis. We study 18,621 people who have side effects while taking Micardis from FDA and social media. Among them, 5 have Creatinine renal clearance increased. Find out below who they are, when they have Creatinine renal clearance increased 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 >>>
Micardis has active ingredients of telmisartan. It is often used in high blood pressure. (latest outcomes from Micardis 19,595 users)
Creatinine renal clearance increased has been reported by people with high blood pressure, type 2 diabetes, diabetes, atrial fibrillation/flutter, osteoporosis (latest reports from 481 Creatinine renal clearance increased patients).
On Oct, 22, 2016
18,621 people reported to have side effects when taking Micardis.
Among them, 5 people (0.03%) have Creatinine Renal Clearance Increased
* 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.
Concerned about relieving sleep apnea to help with memory loss. Taking vinpocetine to improve hearing eyesight, and hopefully, memory I take echinacea to build my immune system and haven't been sick in nine years. I take turmeric to prevent cancer. I take Kombucha and mangosteen ...
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.