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