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