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