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Lidocaine 4% reports
Browse community reports connected to Lidocaine 4%. These reports can show that other people are describing similar experiences, but they do not prove that Lidocaine 4% 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.
36 problems
Abdominal Pain Upper while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and abdominal pain upper appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and abdominal pain appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and anxiety appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and back pain appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and chills appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and constipation appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and cough appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and decreased appetite appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and dehydration appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and diarrhea appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and dizziness appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and fatigue appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and feeling abnormal appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and headache appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and hives appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and hypotension appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and insomnia appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and itching appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and malaise appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and migraine appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and muscle spasms appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and nausea appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and pain appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and peripheral swelling appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and rash appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and shortness of breath appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and skin redness appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and sleepiness appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and swelling appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and tachycardia appear together. This does not establish that Lidocaine 4% 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 Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and tingling or pins and needles appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and tremor appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and vomiting appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and weakness appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and weight decreased appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Lidocaine 4%
FDA FAERS contains adverse-event reports in which Lidocaine 4% and weight increased appear together. This does not establish that Lidocaine 4% caused the reported reaction and cannot be used to estimate how often it occurs.
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