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Ambrisentan reports
Browse community reports connected to Ambrisentan. These reports can show that other people are describing similar experiences, but they do not prove that Ambrisentan 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.
38 problems
Abdominal Discomfort while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and abdominal discomfort appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and abdominal distension appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and abdominal pain upper appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and abdominal pain appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and anxiety appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and back pain appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and chest discomfort appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and constipation appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and cough appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and decreased appetite appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and dehydration appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and diarrhea appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and dizziness appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and dyspepsia appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and fatigue appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and feeling abnormal appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Flushing while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and flushing appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and headache appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and heart rate increased appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and hypotension appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and insomnia appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and itching appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and malaise appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and migraine appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and muscle spasms appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and myalgia appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and nausea appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and oropharyngeal pain appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and pain appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and palpitations appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and peripheral swelling appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and rash appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and shortness of breath appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and swelling appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and vomiting appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and weakness appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and weight decreased appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Ambrisentan
FDA FAERS contains adverse-event reports in which Ambrisentan and weight increased appear together. This does not establish that Ambrisentan caused the reported reaction and cannot be used to estimate how often it occurs.
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