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Ranitidine Hydrochloride reports
Browse community reports connected to Ranitidine Hydrochloride. These reports can show that other people are describing similar experiences, but they do not prove that Ranitidine Hydrochloride 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.
29 problems
Abdominal Discomfort while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and abdominal discomfort appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and abdominal pain upper appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and abdominal pain appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and acid reflux appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and anxiety appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and back pain appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and constipation appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and cough appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and diarrhea appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and dizziness appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and dry mouth appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and excessive sweating appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and fatigue appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and headache appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and hives appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and malaise appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and migraine appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and muscle spasms appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and nausea appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and pain appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash Erythematous while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and rash erythematous appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and rash appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and shortness of breath appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and skin redness appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and swelling appear together. This does not establish that Ranitidine Hydrochloride 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 Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and tingling or pins and needles appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and vomiting appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and weakness appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Ranitidine Hydrochloride
FDA FAERS contains adverse-event reports in which Ranitidine Hydrochloride and weight increased appear together. This does not establish that Ranitidine Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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