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