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Propofol reports
Browse community reports connected to Propofol. These reports can show that other people are describing similar experiences, but they do not prove that Propofol 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.
20 problems
Abdominal Pain while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and abdominal pain appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and anxiety appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and chills appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and cough appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and diarrhea appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and dizziness appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and fatigue appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and headache appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and heart rate increased appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and hives appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and hypotension appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and nausea appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and pain appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and rash appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and shortness of breath appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and skin redness appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and sleepiness appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and tachycardia appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and vomiting appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Propofol
FDA FAERS contains adverse-event reports in which Propofol and weakness appear together. This does not establish that Propofol caused the reported reaction and cannot be used to estimate how often it occurs.
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