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