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