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Cardizem cd Related Nervousness

Official Government Database Reports16
Online Conversations4

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: Pain, Nervousness

Posted By Anonymous in askapatient.com on August 25, 2015 @ 12:00 am

Side Effects: Pains around the chest area, local doc thinks the drug is dilating the osepeaghus causing increased acid and GORD. Lightheadness, nervousness. The drug seems to be doing its t...

Druginformer Identified Side Effects: Tremor, Feeling cold, Fatigue, Chills, Agitation, Lethargy, Loss of consciousness, Sleep disorder, Nervousness, Crying, Palpitations, Anxiety, Depression, Drug ineffective, Dyspnoea, Feeling hot, Heart rate irregular, Hyperhidrosis, Muscular weakness, Rhinorrhoea

Posted By Anonymous in askapatient.com on November 13, 2014 @ 12:00 am

Side Effects: I felt anxious, nervous, agitated, urinating a lot, cold chills back to feeling warm and sweaty, sleep problems, runny nose, depressed, crying, shaky, feeling like my heart was going to...

Druginformer Identified Side Effects: Fatigue, Nervousness, Anxiety, Somnolence

Posted By Anonymous in askapatient.com on July 5, 2007 @ 12:00 am

Side Effects: Weird/nervous feeling when trying to go to sleep, have to be exhausted. Greater fatigue than normal in the afternoon. Anxiousness. Have stopped taking for several days and the...

Druginformer Identified Side Effects: Nervousness, Euphoric mood, Heart rate, Panic reaction

Posted By Anonymous in askapatient.com on April 19, 2006 @ 12:00 am

Side Effects: very light headness almost panicy and jumpy, accelerated heart rate,blood pressure lowered but pulse higher.

* 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.