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