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