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