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Oxaliplatin reports

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

31 problems

Abdominal Pain Upper while using Oxaliplatin

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

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Abdominal Pain while using Oxaliplatin

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

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Back Pain while using Oxaliplatin

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

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Chest Discomfort while using Oxaliplatin

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

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Chills while using Oxaliplatin

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

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Constipation while using Oxaliplatin

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

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Cough while using Oxaliplatin

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

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Decreased Appetite while using Oxaliplatin

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

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Dehydration while using Oxaliplatin

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

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Diarrhea while using Oxaliplatin

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

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Dizziness while using Oxaliplatin

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

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Excessive sweating while using Oxaliplatin

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

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Fatigue while using Oxaliplatin

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

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Flushing while using Oxaliplatin

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

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Headache while using Oxaliplatin

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

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Hypotension while using Oxaliplatin

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

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Itching while using Oxaliplatin

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

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Malaise while using Oxaliplatin

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

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Muscle Spasms while using Oxaliplatin

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

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Nausea while using Oxaliplatin

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

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Pain while using Oxaliplatin

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

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Peripheral swelling while using Oxaliplatin

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

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Rash while using Oxaliplatin

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

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Shortness of breath while using Oxaliplatin

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

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Skin redness while using Oxaliplatin

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

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Tachycardia while using Oxaliplatin

FDA FAERS contains adverse-event reports in which Oxaliplatin and tachycardia appear together. This does not establish that Oxaliplatin 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 Oxaliplatin

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

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Tremor while using Oxaliplatin

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

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Vomiting while using Oxaliplatin

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

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Weakness while using Oxaliplatin

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

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Weight Decreased while using Oxaliplatin

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

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