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