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Review: could Diltiazem cause Gastrointestinal arteriovenous malformation?

We study 6,050 people who have side effects while taking Diltiazem from FDA and social media. Find out below who they are, when they have Gastrointestinal arteriovenous malformation and more.

Diltiazem hydrochloride

Diltiazem hydrochloride (latest outcomes from 6,544 users) has active ingredients of diltiazem hydrochloride. It is often used in high blood pressure.

Gastrointestinal arteriovenous malformation

Gastrointestinal arteriovenous malformation (malformation of arteries and veins in gastrointestinal tract) (latest reports from 1,253 patients) has been reported by people with multiple myeloma, rheumatoid arthritis, high blood pressure, anaemia, pain.

On Oct, 30, 2014: No report is found

Do you have Gastrointestinal Arteriovenous Malformation while taking Diltiazem Hydrochloride?

Get connected! Join a mobile support group:
- support group for people who take Diltiazem hydrochloride
- support group for people who have Gastrointestinal Arteriovenous Malformation

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More reviews for: Diltiazem hydrochloride, Gastrointestinal arteriovenous malformation

On eHealthMe, Diltiazem Hydrochloride (diltiazem hydrochloride) is often used for high blood pressure. Find out below the conditions Diltiazem Hydrochloride is used for, how effective it is, and any alternative drugs that you can use to treat those same conditions.

What is Diltiazem Hydrochloride used for and how effective is it:

Other drugs that are used to treat the same conditions:

Could it be a symptom from a condition:

Drugs in real world that are associated with:

Could your condition cause it?

Related drug studies for: Diltiazem hydrochloride, Gastrointestinal arteriovenous malformation

Recent Diltiazem hydrochloride related drug comparison:

More related comparison studies for: Diltiazem hydrochloride, Gastrointestinal arteriovenous malformation

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.

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You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

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