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Diltiazem Hydrochloride reports

Browse community reports connected to Diltiazem Hydrochloride. These reports can show that other people are describing similar experiences, but they do not prove that Diltiazem Hydrochloride caused a symptom or reaction.

⚕️ Medicine safety note

Community reports do not prove causation, cannot be used to estimate how common a reaction is, and are not medical advice.

41 problems

Abdominal Discomfort while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and abdominal discomfort appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain Upper while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and abdominal pain upper appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and abdominal pain appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Alopecia while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and alopecia appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and anxiety appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and back pain appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Chills while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and chills appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and constipation appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and cough appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and decreased appetite appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and dehydration appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and diarrhea appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and dizziness appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and fatigue appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and feeling abnormal appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and headache appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Heart Rate Increased while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and heart rate increased appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Hives while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and hives appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and hypotension appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and insomnia appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and itching appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and malaise appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and muscle spasms appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscular Weakness while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and muscular weakness appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Myalgia while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and myalgia appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and nausea appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and pain appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Palpitations while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and palpitations appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and peripheral swelling appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and rash appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and shortness of breath appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleep Disorder while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and sleep disorder appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and sleepiness appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Swelling while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and swelling appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Tachycardia while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and tachycardia appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Tingling or pins and needles while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and tingling or pins and needles appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and tremor appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and vomiting appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and weakness appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and weight decreased appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Increased while using Diltiazem Hydrochloride

FDA FAERS contains adverse-event reports in which Diltiazem Hydrochloride and weight increased appear together. This does not establish that Diltiazem Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.

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