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