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