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