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