There is no Gastrointestinal arteriovenous malformation reported by people who take Diltiazem hydrochloride yet. We study 2,148 people who have side effects while taking Diltiazem hydrochloride from FDA and social media. Find out below who they are, when they have Gastrointestinal arteriovenous malformation 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 >>>
Diltiazem hydrochloride has active ingredients of diltiazem hydrochloride. It is often used in high blood pressure. (latest outcomes from Diltiazem hydrochloride 5,919 users)
Gastrointestinal arteriovenous malformation (malformation of arteries and veins in gastrointestinal tract) (latest reports from 141 Gastrointestinal arteriovenous malformation patients).
On Jul, 24, 2016
No report is found.
Taking Cardzem 120 XT two times per day for cardiac arrhythmia post pneumonia. 61+ years. Skip a dose on occasion and NO hot flashes. Taken as prescribed and hot flashes start within 30 mins of ingestion. Try to take 2nd dose between 6-7 PM ti help reduce severity of nightime flashes and insomnia.
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.