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Clonidine reports

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

38 problems

Abdominal Discomfort while using Clonidine

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

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Abdominal Pain Upper while using Clonidine

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

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Abdominal Pain while using Clonidine

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

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Alopecia while using Clonidine

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

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Anxiety while using Clonidine

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

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Back Pain while using Clonidine

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

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Constipation while using Clonidine

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

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Cough while using Clonidine

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

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Decreased Appetite while using Clonidine

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

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Dehydration while using Clonidine

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

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Diarrhea while using Clonidine

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

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Dizziness while using Clonidine

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

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Excessive sweating while using Clonidine

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

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Fatigue while using Clonidine

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

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Feeling Abnormal while using Clonidine

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

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Headache while using Clonidine

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

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Heart Rate Increased while using Clonidine

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

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Hypotension while using Clonidine

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

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Insomnia while using Clonidine

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

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Itching while using Clonidine

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

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Malaise while using Clonidine

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

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Muscle Spasms while using Clonidine

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

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Muscular Weakness while using Clonidine

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

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Myalgia while using Clonidine

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

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Nausea while using Clonidine

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

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Pain while using Clonidine

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

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Peripheral swelling while using Clonidine

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

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Rash Erythematous while using Clonidine

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

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Rash while using Clonidine

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

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Shortness of breath while using Clonidine

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

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Skin redness while using Clonidine

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

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Sleepiness while using Clonidine

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

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Tremor while using Clonidine

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

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Vision Blurred while using Clonidine

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

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Vomiting while using Clonidine

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

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Weakness while using Clonidine

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

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Weight Decreased while using Clonidine

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

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Weight Increased while using Clonidine

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

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