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