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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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Druginformer Identified Side Effects: Crying, Anxiety, Depression, Hot flush

Posted By Anonymous in askapatient.com on November 22, 2014 @ 12:00 am

Side Effects: Hot flashes, anxiety, depression, crying,

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on November 18, 2014 @ 12:00 am

Side Effects:

Druginformer Identified Side Effects: Chills, Crying, Palpitations, Anxiety, Sneezing, Depression, Muscular weakness, Rhinorrhoea, Somnolence

Posted By Anonymous in askapatient.com on November 12, 2014 @ 12:00 am

Side Effects: Runny nose, sneezing, tiredness, really weak, warm, chills, depressed, anxious, not myself, urinating a lot, palpitations still there at times not getting better, crying spells, tried f...

Druginformer Identified Side Effects: Abdominal discomfort, Blood pressure decreased

Posted By Anonymous in everydayhealth.com on June 3, 2013 @ 12:00 am

... stage 2 hypertension tried lopresor 50 a day then 100 a day they made me tired for the first week then I was better and i didnt like the fact that i had to eat a lot to avoid stomache upset and my bp...

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on March 30, 2012 @ 12:00 am

Side Effects: None that I noticed. Wonderful, miracle cure for heart palpitations. Unfortunately, counter indicated with Latuda, which I start a few months ago. (Raises the serum levels o...

Druginformer Identified Side Effects: Regurgitation, Fatigue, Decompression sickness, Cough, Muscular weakness, Respiration abnormal, General physical health deterioration

Posted By Anonymous in askapatient.com on December 22, 2011 @ 12:00 am

... A couple of times I couldn't breathe, my oesophagus completely closed so I took 2 types of antihistamine which helped. Also the last time I woke up I coughed until I was spitting up blood. I have also...

Druginformer Identified Side Effects: Abdominal pain, Endoscopy, Abdominal pain upper, Burn oesophageal

Posted By Anonymous in askapatient.com on December 20, 2011 @ 12:00 am

Side Effects: Had experienced burning up oesophagus after taking Cardizem for approx 8 months. Have had stomach burning and pain for 2 months. ENDOSCOPY TODAY diagonised ulcers!! I ceased Cardizem...

Druginformer Identified Side Effects: Fatigue, Dizziness, Flushing, Lethargy, Tinnitus, Somnolence, Hot flush

Posted By Anonymous in askapatient.com on March 23, 2011 @ 12:00 am

Side Effects: When I first started, ringing in ears, hot flashes/flushed. Tired all the time. Basic walking and tasks a chore, just beyond tired. Makes driving hard, maybe because I feel dizzy an...

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on January 6, 2011 @ 12:00 am

Side Effects:

Druginformer Identified Side Effects: Blood pressure increased

Posted By Anonymous in everydayhealth.com on October 23, 2010 @ 12:00 am

blood pressure is still high.


* 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.