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