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