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