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Cyclosporine reports
Browse community reports connected to Cyclosporine. These reports can show that other people are describing similar experiences, but they do not prove that Cyclosporine 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.
29 problems
Abdominal Pain while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and abdominal pain appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and alopecia appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and anxiety appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and back pain appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and cough appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and decreased appetite appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and diarrhea appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and dizziness appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Eye while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and dry eye appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Irritation while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and eye irritation appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Pain while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and eye pain appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and fatigue appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and headache appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and hives appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and insomnia appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and itching appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and malaise appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and myalgia appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and nausea appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and pain appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and rash appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and shortness of breath appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and skin redness appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and vision blurred appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and vomiting appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Watery eyes while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and watery eyes appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and weakness appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and weight decreased appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Cyclosporine
FDA FAERS contains adverse-event reports in which Cyclosporine and weight increased appear together. This does not establish that Cyclosporine caused the reported reaction and cannot be used to estimate how often it occurs.
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