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Ramipril reports
Browse community reports connected to Ramipril. These reports can show that other people are describing similar experiences, but they do not prove that Ramipril 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.
34 problems
Abdominal Discomfort while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and abdominal discomfort appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and abdominal pain upper appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and abdominal pain appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and alopecia appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and anxiety appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and back pain appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and cough appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and decreased appetite appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and dehydration appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and diarrhea appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and dizziness appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and dry mouth appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and fatigue appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and headache appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and hives appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and hypotension appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and insomnia appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and itching appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and malaise appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and muscle spasms appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and muscular weakness appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and myalgia appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and nausea appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and pain appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and peripheral swelling appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and rash appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and shortness of breath appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and sleep disorder appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and swelling appear together. This does not establish that Ramipril 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 Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and tingling or pins and needles appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and vomiting appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and weakness appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and weight decreased appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Ramipril
FDA FAERS contains adverse-event reports in which Ramipril and weight increased appear together. This does not establish that Ramipril caused the reported reaction and cannot be used to estimate how often it occurs.
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