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