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Varenicline Tartrate reports
Browse community reports connected to Varenicline Tartrate. These reports can show that other people are describing similar experiences, but they do not prove that Varenicline Tartrate 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 Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and abdominal discomfort appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and abdominal distension appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and abdominal pain upper appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and abdominal pain appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and anxiety appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and back pain appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and constipation appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and cough appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and decreased appetite appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and diarrhea appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and dizziness appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and dry mouth appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and dyspepsia appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and excessive sweating appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and fatigue appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and feeling abnormal appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Flatulence while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and flatulence appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and headache appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and heart rate increased appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and hives appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and insomnia appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Irritability while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and irritability appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and itching appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and malaise appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and migraine appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and muscle spasms appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and myalgia appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and nausea appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Nervousness while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and nervousness appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and pain appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and palpitations appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and rash appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and shortness of breath appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and sleep disorder appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and sleepiness appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Taste changes while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and taste changes appear together. This does not establish that Varenicline Tartrate 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 Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and tingling or pins and needles appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and tremor appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and vision blurred appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and vomiting appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and weakness appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and weight decreased appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Varenicline Tartrate
FDA FAERS contains adverse-event reports in which Varenicline Tartrate and weight increased appear together. This does not establish that Varenicline Tartrate caused the reported reaction and cannot be used to estimate how often it occurs.
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