HappeningToo topic
0xygen reports
Browse community reports connected to 0xygen. These reports can show that other people are describing similar experiences, but they do not prove that 0xygen 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 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and abdominal discomfort appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and abdominal distension appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and abdominal pain upper appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and abdominal pain appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and anxiety appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and back pain appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and chest discomfort appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and constipation appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and cough appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and decreased appetite appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and dehydration appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and diarrhea appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and dizziness appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and fatigue appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and feeling abnormal appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Flushing while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and flushing appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and headache appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and heart rate increased appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and hypotension appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and insomnia appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and itching appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and malaise appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and muscle spasms appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and myalgia appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and nausea appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and oropharyngeal pain appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and pain appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and palpitations appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and peripheral swelling appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and rash appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and shortness of breath appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and skin redness appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and sleepiness appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and swelling appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and tremor appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and vomiting appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and weakness appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and weight decreased appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using 0xygen
FDA FAERS contains adverse-event reports in which 0xygen and weight increased appear together. This does not establish that 0xygen caused the reported reaction and cannot be used to estimate how often it occurs.
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