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