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