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Tramadol Hydrochloride reports
Browse community reports connected to Tramadol Hydrochloride. These reports can show that other people are describing similar experiences, but they do not prove that Tramadol 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.
30 problems
Abdominal Discomfort while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and abdominal discomfort appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and abdominal pain upper appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and abdominal pain appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and acid reflux appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and alopecia appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and anxiety appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and back pain appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and decreased appetite appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and diarrhea appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and dizziness appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and dry mouth appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and fatigue appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and headache appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and hives appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and insomnia appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and itching appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and malaise appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and muscle spasms appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and nausea appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and pain appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and rash appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and shortness of breath appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and sleep disorder appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and sleepiness appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and swelling appear together. This does not establish that Tramadol Hydrochloride 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 Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and tingling or pins and needles appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and vomiting appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and weakness appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and weight decreased appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Tramadol Hydrochloride
FDA FAERS contains adverse-event reports in which Tramadol Hydrochloride and weight increased appear together. This does not establish that Tramadol Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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