HappeningToo topic
Exenatide reports
Browse community reports connected to Exenatide. These reports can show that other people are describing similar experiences, but they do not prove that Exenatide 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.
45 problems
Abdominal Discomfort while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and abdominal discomfort appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Distension while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and abdominal distension appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain Upper while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and abdominal pain upper appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and abdominal pain appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Acid reflux while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and acid reflux appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Anxiety while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and anxiety appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Back Pain while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and back pain appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Chills while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and chills appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Constipation while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and constipation appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Cough while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and cough appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Decreased Appetite while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and decreased appetite appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dehydration while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and dehydration appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Diarrhea while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and diarrhea appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dizziness while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and dizziness appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dyspepsia while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and dyspepsia appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Excessive sweating while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and excessive sweating appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Fatigue while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and fatigue appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Feeling Abnormal while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and feeling abnormal appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Feeling Cold while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and feeling cold appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Flatulence while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and flatulence appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Headache while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and headache appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Heart Rate Increased while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and heart rate increased appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Hives while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and hives appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Increased Appetite while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and increased appetite appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Insomnia while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and insomnia appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Itching while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and itching appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Malaise while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and malaise appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Muscle Spasms while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and muscle spasms appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Nausea while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and nausea appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Nervousness while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and nervousness appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Pain while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and pain appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Palpitations while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and palpitations appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Peripheral swelling while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and peripheral swelling appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Rash while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and rash appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Shortness of breath while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and shortness of breath appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Sleepiness while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and sleepiness appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Stomach Discomfort while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and stomach discomfort appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Taste changes while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and taste changes appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Tingling or pins and needles while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and tingling or pins and needles appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Tremor while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and tremor appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Vision Blurred while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and vision blurred appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Vomiting while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and vomiting appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weakness while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and weakness appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Decreased while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and weight decreased appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Increased while using Exenatide
FDA FAERS contains adverse-event reports in which Exenatide and weight increased appear together. This does not establish that Exenatide caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →