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Ciprofolxacin reports
Browse community reports connected to Ciprofolxacin. These reports can show that other people are describing similar experiences, but they do not prove that Ciprofolxacin 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.
46 problems
Abdominal Discomfort while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and abdominal discomfort appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and abdominal pain upper appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and abdominal pain appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and acid reflux appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and alopecia appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and anxiety appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and back pain appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Burning Sensation while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and burning sensation appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and chills appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and constipation appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and cough appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and decreased appetite appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and dehydration appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and diarrhea appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and dizziness appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and dyspepsia appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and excessive sweating appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and fatigue appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and feeling abnormal appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and headache appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and hives appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and hypotension appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and insomnia appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and itching appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and malaise appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and muscle spasms appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and muscular weakness appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and myalgia appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and nausea appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and pain appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and palpitations appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and peripheral swelling appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and rash appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and shortness of breath appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and skin redness appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and sleepiness appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and swelling appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and tachycardia appear together. This does not establish that Ciprofolxacin 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 Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and tingling or pins and needles appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Tinnitus while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and tinnitus appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and tremor appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and vision blurred appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and vomiting appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and weakness appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and weight decreased appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Ciprofolxacin
FDA FAERS contains adverse-event reports in which Ciprofolxacin and weight increased appear together. This does not establish that Ciprofolxacin caused the reported reaction and cannot be used to estimate how often it occurs.
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