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