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