Topiramate reports

Abdominal Discomfort while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and abdominal discomfort appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain Upper while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and abdominal pain upper appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and abdominal pain appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Acid reflux while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and acid reflux appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Alopecia while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and alopecia appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and anxiety appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and back pain appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and constipation appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and cough appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and decreased appetite appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and diarrhea appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and dizziness appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Dry Mouth while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and dry mouth appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Dyspepsia while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and dyspepsia appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and excessive sweating appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and fatigue appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and feeling abnormal appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and headache appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Hives while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and hives appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and hypotension appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and insomnia appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and itching appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and malaise appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Migraine while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and migraine appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and muscle spasms appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscular Weakness while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and muscular weakness appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and nausea appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Neck Pain while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and neck pain appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and pain appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and rash appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and shortness of breath appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleep Disorder while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and sleep disorder appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and sleepiness appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Swelling while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and swelling appear together. This does not establish that Topiramate 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 Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and tingling or pins and needles appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and tremor appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Vision Blurred while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and vision blurred appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and vomiting appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and weakness appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and weight decreased appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Increased while using Topiramate

FDA FAERS contains adverse-event reports in which Topiramate and weight increased appear together. This does not establish that Topiramate caused the reported reaction and cannot be used to estimate how often it occurs.

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