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