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Amlodipine reports
Browse community reports connected to Amlodipine. These reports can show that other people are describing similar experiences, but they do not prove that Amlodipine 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 Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and abdominal discomfort appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and abdominal distension appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and abdominal pain upper appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and abdominal pain appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and alopecia appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and anxiety appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and back pain appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and chest discomfort appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and constipation appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and cough appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and decreased appetite appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and dehydration appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and diarrhea appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and dizziness appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and dyspepsia appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and fatigue appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and feeling abnormal appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and headache appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and heart rate increased appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and hypotension appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and insomnia appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and itching appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and malaise appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and muscle spasms appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and muscular weakness appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and myalgia appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and nausea appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and pain appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and palpitations appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and peripheral swelling appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and rash appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and shortness of breath appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and skin redness appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and sleepiness appear together. This does not establish that Amlodipine 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 Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and tingling or pins and needles appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and tremor appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and vision blurred appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and vomiting appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and weakness appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and weight decreased appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Amlodipine
FDA FAERS contains adverse-event reports in which Amlodipine and weight increased appear together. This does not establish that Amlodipine caused the reported reaction and cannot be used to estimate how often it occurs.
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