Ondansetron reports

Abdominal Discomfort while using Ondansetron

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

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Abdominal Distension while using Ondansetron

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

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Abdominal Pain Upper while using Ondansetron

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

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Abdominal Pain while using Ondansetron

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

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Alopecia while using Ondansetron

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

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Anxiety while using Ondansetron

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

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Back Pain while using Ondansetron

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

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Chest Discomfort while using Ondansetron

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

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Chills while using Ondansetron

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

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Constipation while using Ondansetron

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

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Cough while using Ondansetron

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

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Decreased Appetite while using Ondansetron

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

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Dehydration while using Ondansetron

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

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Diarrhea while using Ondansetron

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

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Dizziness while using Ondansetron

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

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Excessive sweating while using Ondansetron

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

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Fatigue while using Ondansetron

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

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Feeling Abnormal while using Ondansetron

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

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Headache while using Ondansetron

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

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Hypotension while using Ondansetron

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

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Insomnia while using Ondansetron

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

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Itching while using Ondansetron

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

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Malaise while using Ondansetron

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

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Muscle Spasms while using Ondansetron

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

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Muscular Weakness while using Ondansetron

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

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Myalgia while using Ondansetron

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

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Nausea while using Ondansetron

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

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Pain while using Ondansetron

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

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Peripheral swelling while using Ondansetron

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

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Rash while using Ondansetron

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

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Shortness of breath while using Ondansetron

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

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Skin redness while using Ondansetron

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

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Sleepiness while using Ondansetron

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

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Tachycardia while using Ondansetron

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

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

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Tremor while using Ondansetron

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

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Vomiting while using Ondansetron

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

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Weakness while using Ondansetron

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

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Weight Decreased while using Ondansetron

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

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Weight Increased while using Ondansetron

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

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