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