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