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Multivitamin reports

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

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

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Abdominal Distension while using Multivitamin

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

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Abdominal Pain Upper while using Multivitamin

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

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Abdominal Pain while using Multivitamin

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

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Acid reflux while using Multivitamin

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

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Alopecia while using Multivitamin

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

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Anxiety while using Multivitamin

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

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Back Pain while using Multivitamin

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

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Chest Discomfort while using Multivitamin

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

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Chills while using Multivitamin

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

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Constipation while using Multivitamin

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

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Cough while using Multivitamin

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

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Decreased Appetite while using Multivitamin

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

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Dehydration while using Multivitamin

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

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Diarrhea while using Multivitamin

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

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Dizziness while using Multivitamin

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

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Dry Mouth while using Multivitamin

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

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Dry Skin while using Multivitamin

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

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Dyspepsia while using Multivitamin

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

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Excessive sweating while using Multivitamin

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

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Fatigue while using Multivitamin

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

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Feeling Abnormal while using Multivitamin

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

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Flushing while using Multivitamin

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

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Headache while using Multivitamin

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

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Heart Rate Increased while using Multivitamin

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

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Hives while using Multivitamin

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

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Hot Flush while using Multivitamin

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

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Hypotension while using Multivitamin

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

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Influenza Like Illness while using Multivitamin

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

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Insomnia while using Multivitamin

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

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Itching while using Multivitamin

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

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Malaise while using Multivitamin

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

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Migraine while using Multivitamin

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

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Muscle Spasms while using Multivitamin

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

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Muscular Weakness while using Multivitamin

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

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Myalgia while using Multivitamin

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

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Nausea while using Multivitamin

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

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Oropharyngeal Pain while using Multivitamin

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

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Pain while using Multivitamin

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

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Palpitations while using Multivitamin

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

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Peripheral swelling while using Multivitamin

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

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Rash while using Multivitamin

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

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Shortness of breath while using Multivitamin

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

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Skin redness while using Multivitamin

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

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Sleepiness while using Multivitamin

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

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Taste changes while using Multivitamin

FDA FAERS contains adverse-event reports in which Multivitamin and taste changes appear together. This does not establish that Multivitamin 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 Multivitamin

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

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Tremor while using Multivitamin

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

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Vision Blurred while using Multivitamin

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

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Vomiting while using Multivitamin

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

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Weakness while using Multivitamin

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

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Weight Decreased while using Multivitamin

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

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Weight Increased while using Multivitamin

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

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