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