Ergocalciferol reports

Abdominal Discomfort while using Ergocalciferol

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

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Abdominal Distension while using Ergocalciferol

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

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Abdominal Pain Upper while using Ergocalciferol

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

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Abdominal Pain while using Ergocalciferol

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

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Acid reflux while using Ergocalciferol

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

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Alopecia while using Ergocalciferol

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

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Anxiety while using Ergocalciferol

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

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Back Pain while using Ergocalciferol

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

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Chills while using Ergocalciferol

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

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Constipation while using Ergocalciferol

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

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Cough while using Ergocalciferol

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

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Decreased Appetite while using Ergocalciferol

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

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Dehydration while using Ergocalciferol

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

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Diarrhea while using Ergocalciferol

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

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Dizziness while using Ergocalciferol

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

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Dry Mouth while using Ergocalciferol

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

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Dyspepsia while using Ergocalciferol

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

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Fatigue while using Ergocalciferol

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

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Feeling Abnormal while using Ergocalciferol

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

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Flushing while using Ergocalciferol

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

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Headache while using Ergocalciferol

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

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Hives while using Ergocalciferol

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

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Hypotension while using Ergocalciferol

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

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Insomnia while using Ergocalciferol

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

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Itching while using Ergocalciferol

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

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Malaise while using Ergocalciferol

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

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Migraine while using Ergocalciferol

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

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Muscle Spasms while using Ergocalciferol

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

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Muscular Weakness while using Ergocalciferol

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

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Myalgia while using Ergocalciferol

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

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Nausea while using Ergocalciferol

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

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Pain while using Ergocalciferol

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

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Palpitations while using Ergocalciferol

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

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Peripheral swelling while using Ergocalciferol

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

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Rash while using Ergocalciferol

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

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Shortness of breath while using Ergocalciferol

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

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Skin redness while using Ergocalciferol

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

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Sleepiness while using Ergocalciferol

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

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Swelling while using Ergocalciferol

FDA FAERS contains adverse-event reports in which Ergocalciferol and swelling appear together. This does not establish that Ergocalciferol 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 Ergocalciferol

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

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Tremor while using Ergocalciferol

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

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Vision Blurred while using Ergocalciferol

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

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Vomiting while using Ergocalciferol

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

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Weakness while using Ergocalciferol

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

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Weight Decreased while using Ergocalciferol

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

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Weight Increased while using Ergocalciferol

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

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