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