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