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