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Voriconazole reports
Browse community reports connected to Voriconazole. These reports can show that other people are describing similar experiences, but they do not prove that Voriconazole 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.
22 problems
Abdominal Pain while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and abdominal pain appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and constipation appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and cough appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and decreased appetite appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and diarrhea appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and dizziness appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and fatigue appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and headache appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and hypotension appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and insomnia appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and malaise appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and nausea appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and pain appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and peripheral swelling appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and rash appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and shortness of breath appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and skin redness appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and tremor appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and vision blurred appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and vomiting appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and weakness appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Voriconazole
FDA FAERS contains adverse-event reports in which Voriconazole and weight decreased appear together. This does not establish that Voriconazole caused the reported reaction and cannot be used to estimate how often it occurs.
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