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