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Candesartan reports
Browse community reports connected to Candesartan. These reports can show that other people are describing similar experiences, but they do not prove that Candesartan 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.
35 problems
Abdominal Discomfort while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and abdominal discomfort appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and abdominal pain upper appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and abdominal pain appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and acid reflux appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and alopecia appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and anxiety appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and back pain appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and cough appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and decreased appetite appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and diarrhea appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and dizziness appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and dry mouth appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and dyspepsia appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and fatigue appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and headache appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and hives appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and hypotension appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and insomnia appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and itching appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and malaise appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and migraine appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and muscle spasms appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and muscular weakness appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and nausea appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and pain appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and palpitations appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and rash appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and shortness of breath appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and sleep disorder appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and swelling appear together. This does not establish that Candesartan 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 Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and tingling or pins and needles appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and vomiting appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and weakness appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and weight decreased appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Candesartan
FDA FAERS contains adverse-event reports in which Candesartan and weight increased appear together. This does not establish that Candesartan caused the reported reaction and cannot be used to estimate how often it occurs.
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