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