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Naltrexone reports
Browse community reports connected to Naltrexone. These reports can show that other people are describing similar experiences, but they do not prove that Naltrexone 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.
35 problems
Abdominal Discomfort while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and abdominal discomfort appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and abdominal pain upper appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and abdominal pain appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and anxiety appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and back pain appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and chills appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and constipation appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and cough appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and decreased appetite appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and diarrhea appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and dizziness appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and excessive sweating appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and fatigue appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and feeling abnormal appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and headache appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Influenza Like Illness while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and influenza like illness appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and insomnia appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Irritability while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and irritability appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and itching appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and malaise appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and migraine appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and muscle spasms appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and myalgia appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and nausea appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and pain appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and rash appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Restlessness while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and restlessness appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and shortness of breath appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and sleepiness appear together. This does not establish that Naltrexone 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 Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and tingling or pins and needles appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and tremor appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and vomiting appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and weakness appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and weight decreased appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Naltrexone
FDA FAERS contains adverse-event reports in which Naltrexone and weight increased appear together. This does not establish that Naltrexone caused the reported reaction and cannot be used to estimate how often it occurs.
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