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