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Dabigatran Etexilate reports
Browse community reports connected to Dabigatran Etexilate. These reports can show that other people are describing similar experiences, but they do not prove that Dabigatran Etexilate 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.
29 problems
Abdominal Discomfort while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and abdominal discomfort appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and abdominal pain upper appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and abdominal pain appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and acid reflux appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and back pain appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and chest discomfort appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and constipation appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and cough appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and decreased appetite appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and dehydration appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and diarrhea appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and dizziness appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and dyspepsia appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and fatigue appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and feeling abnormal appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Flatulence while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and flatulence appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and headache appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and hypotension appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and insomnia appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and itching appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and malaise appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and nausea appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and pain appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and peripheral swelling appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and rash appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and shortness of breath appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and vomiting appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and weakness appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Dabigatran Etexilate
FDA FAERS contains adverse-event reports in which Dabigatran Etexilate and weight decreased appear together. This does not establish that Dabigatran Etexilate caused the reported reaction and cannot be used to estimate how often it occurs.
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