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