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