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