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