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