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Amoxicillin reports
Browse community reports connected to Amoxicillin. These reports can show that other people are describing similar experiences, but they do not prove that Amoxicillin 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 Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and abdominal discomfort appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and abdominal pain upper appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and abdominal pain appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and acid reflux appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and anxiety appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and back pain appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and chest discomfort appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and chills appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and constipation appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and cough appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and decreased appetite appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and dehydration appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and diarrhea appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and dizziness appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and dyspepsia appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and fatigue appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and feeling abnormal appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and headache appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and hives appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and hypotension appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and insomnia appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and itching appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and malaise appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and muscle spasms appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and myalgia appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and nausea appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and oropharyngeal pain appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and pain appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and palpitations appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and peripheral swelling appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash Maculo-papular while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and rash maculo-papular appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and rash appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and shortness of breath appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and skin redness appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and sleepiness appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Tingling or pins and needles while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and tingling or pins and needles appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and tremor appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and vomiting appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and weakness appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and weight decreased appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Amoxicillin
FDA FAERS contains adverse-event reports in which Amoxicillin and weight increased appear together. This does not establish that Amoxicillin caused the reported reaction and cannot be used to estimate how often it occurs.
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