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