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