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