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Dalfampridine reports
Browse community reports connected to Dalfampridine. These reports can show that other people are describing similar experiences, but they do not prove that Dalfampridine 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.
35 problems
Abdominal Discomfort while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and abdominal discomfort appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and abdominal pain upper appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and alopecia appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and anxiety appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and back pain appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Burning Sensation while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and burning sensation appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and chills appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and constipation appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and cough appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and diarrhea appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and dizziness appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and fatigue appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and feeling abnormal appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Flushing while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and flushing appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and headache appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Hot Flush while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and hot flush appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Influenza Like Illness while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and influenza like illness appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and insomnia appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and itching appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and malaise appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and muscle spasms appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and muscular weakness appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and nausea appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and pain appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and rash appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and shortness of breath appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and skin redness appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and sleepiness appear together. This does not establish that Dalfampridine 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 Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and tingling or pins and needles appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and tremor appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and vision blurred appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and vomiting appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and weakness appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and weight decreased appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Dalfampridine
FDA FAERS contains adverse-event reports in which Dalfampridine and weight increased appear together. This does not establish that Dalfampridine caused the reported reaction and cannot be used to estimate how often it occurs.
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