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Enalapril reports

Browse community reports connected to Enalapril. These reports can show that other people are describing similar experiences, but they do not prove that Enalapril 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.

37 problems

Abdominal Discomfort while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and abdominal discomfort appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain Upper while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and abdominal pain upper appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and abdominal pain appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and anxiety appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and back pain appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and constipation appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and cough appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and decreased appetite appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and dehydration appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and diarrhea appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and dizziness appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and excessive sweating appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and fatigue appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and feeling abnormal appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and headache appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and hypotension appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and insomnia appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and itching appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and malaise appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and muscle spasms appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscular Weakness while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and muscular weakness appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Myalgia while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and myalgia appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and nausea appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and pain appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and peripheral swelling appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and rash appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and shortness of breath appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and skin redness appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and sleepiness appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Tachycardia while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and tachycardia appear together. This does not establish that Enalapril 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 Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and tingling or pins and needles appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and tremor appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Vision Blurred while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and vision blurred appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and vomiting appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and weakness appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and weight decreased appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Increased while using Enalapril

FDA FAERS contains adverse-event reports in which Enalapril and weight increased appear together. This does not establish that Enalapril caused the reported reaction and cannot be used to estimate how often it occurs.

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