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