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