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Cardizem Related Muscular weakness

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Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.


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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: 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: Fatigue, Muscular weakness

Posted By Anonymous in drugs.com on September 4, 2009 @ 12:00 am

I have been on this medicine for two months. I have had one attack since I started. I do feel a little tired and weak but no other side effects.

Druginformer Identified Side Effects: Chest pain, Muscular weakness, Somnolence, Exercise tolerance decreased

Posted By Anonymous in askapatient.com on December 3, 2008 @ 12:00 am

Side Effects: weakness, fatigue, decreasing exercise tolerance before experiencing chest pain


* 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.