Losartan reports

Abdominal Discomfort while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and abdominal discomfort appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Distension while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and abdominal distension appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain Upper while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and abdominal pain upper appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and abdominal pain appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Acid reflux while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and acid reflux appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Alopecia while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and alopecia appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and anxiety appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and back pain appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and constipation appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and cough appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and decreased appetite appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and dehydration appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and diarrhea appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and dizziness appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Dry Mouth while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and dry mouth appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Dry Skin while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and dry skin appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Dyspepsia while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and dyspepsia appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and excessive sweating appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and fatigue appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and feeling abnormal appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and headache appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Heart Rate Increased while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and heart rate increased appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and hypotension appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and insomnia appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and itching appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and malaise appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and muscle spasms appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscular Weakness while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and muscular weakness appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Myalgia while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and myalgia appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and nausea appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and pain appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Palpitations while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and palpitations appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and peripheral swelling appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and rash appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and shortness of breath appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and skin redness appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and sleepiness appear together. This does not establish that Losartan 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

FDA FAERS contains adverse-event reports in which Losartan and tingling or pins and needles appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and tremor appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Vision Blurred while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and vision blurred appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and vomiting appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and weakness appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and weight decreased appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Increased while using Losartan

FDA FAERS contains adverse-event reports in which Losartan and weight increased appear together. This does not establish that Losartan caused the reported reaction and cannot be used to estimate how often it occurs.

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