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Celecoxib reports
Browse community reports connected to Celecoxib. These reports can show that other people are describing similar experiences, but they do not prove that Celecoxib 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.
34 problems
Abdominal Discomfort while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and abdominal discomfort appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and abdominal pain upper appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and abdominal pain appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and acid reflux appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and alopecia appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and anxiety appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and back pain appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and cough appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and decreased appetite appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and diarrhea appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and dizziness appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and dry mouth appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and dyspepsia appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and fatigue appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and feeling abnormal appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and headache appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and hives appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and insomnia appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and itching appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and malaise appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and migraine appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and muscle spasms appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and nausea appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and pain appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and peripheral swelling appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and rash appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and shortness of breath appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and sleep disorder appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and swelling appear together. This does not establish that Celecoxib 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 Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and tingling or pins and needles appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and vomiting appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and weakness appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and weight decreased appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Celecoxib
FDA FAERS contains adverse-event reports in which Celecoxib and weight increased appear together. This does not establish that Celecoxib caused the reported reaction and cannot be used to estimate how often it occurs.
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