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Vancomycin reports

Browse community reports connected to Vancomycin. These reports can show that other people are describing similar experiences, but they do not prove that Vancomycin 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.

24 problems

Abdominal Pain while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and abdominal pain appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and anxiety appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Chills while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and chills appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and cough appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and dehydration appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and diarrhea appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and dizziness appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and fatigue appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and headache appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Hives while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and hives appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and hypotension appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and itching appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and malaise appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and nausea appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and pain appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and peripheral swelling appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash Maculo-papular while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and rash maculo-papular appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and rash appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and shortness of breath appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and skin redness appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Tachycardia while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and tachycardia appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and vomiting appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and weakness appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Vancomycin

FDA FAERS contains adverse-event reports in which Vancomycin and weight decreased appear together. This does not establish that Vancomycin caused the reported reaction and cannot be used to estimate how often it occurs.

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