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