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Cardizem

Average User Review Score
* Based on 27 reviews from across the web.
Wikipedia

Diltiazem (INN) (/dɪlˈtaɪəzɛm/) is a nondihydropyridines (non-DHP) calcium channel blocker used in the treatment of hypertension, angina pectoris, and some types of arrhythmia. It relaxes the smooth muscles in the walls of arteries, which opens (dilates) the arteries, allows blood to flow more easily, and lowers blood pressure. Additionally, it lowers blood pressure by acting on the heart itself to reduce the rate, strength, and conduction speed of each beat.

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* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Posted By changingthenameofmentalillness in facebook.com on January 8, 2014 @ 12:00 am

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Posted By 588398401230870 in facebook.com on December 10, 2013 @ 12:00 am

I was put on something similar...a calcium channel blocker. It is a low dose of 30 mg twice a day. It works wonders for my POTS and chest pain. I have not had any side effects at this dose. I also hav...

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Posted By survivin_off_faith in healingwell.com on November 18, 2013 @ 12:00 am

Thanks for sharing your story. I have been dealing with tachycardia and PVC for over 4months now. I had a heart ablation, in August, which improved my problems a lot but not completely. I currently ta...

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Posted By earlyon in www.dailystrength.org on November 13, 2013 @ 12:00 am

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Posted By rockysmom44 in www.dailystrength.org on October 12, 2013 @ 12:00 am

Should I have ablation? I have lived long enough to have lots of issues in my life. I am 68. In my 40's I began having PVC's brought on by nothing in particular but terrifying to me.My cardiologist pu...


* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.