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