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Insulin Human reports
Browse community reports connected to Insulin Human. These reports can show that other people are describing similar experiences, but they do not prove that Insulin Human 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.
30 problems
Abdominal Pain Upper while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and abdominal pain upper appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and abdominal pain appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and anxiety appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and back pain appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and constipation appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and cough appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and decreased appetite appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and dehydration appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and diarrhea appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and dizziness appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and excessive sweating appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and fatigue appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and feeling abnormal appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and headache appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and hypotension appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and insomnia appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and itching appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and malaise appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and nausea appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and pain appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and peripheral swelling appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and rash appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and shortness of breath appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and sleepiness appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and tremor appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and vision blurred appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and vomiting appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and weakness appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and weight decreased appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Insulin Human
FDA FAERS contains adverse-event reports in which Insulin Human and weight increased appear together. This does not establish that Insulin Human caused the reported reaction and cannot be used to estimate how often it occurs.
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