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