HappeningToo topic
Tacrolimus reports
Browse community reports connected to Tacrolimus. These reports can show that other people are describing similar experiences, but they do not prove that Tacrolimus 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.
21 problems
Abdominal Pain while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and abdominal pain appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and alopecia appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and cough appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and decreased appetite appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and dehydration appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and diarrhea appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and dizziness appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and fatigue appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and headache appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and hypotension appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and itching appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and malaise appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and nausea appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and pain appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and rash appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and shortness of breath appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and skin redness appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and tremor appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and vomiting appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and weakness appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Tacrolimus
FDA FAERS contains adverse-event reports in which Tacrolimus and weight decreased appear together. This does not establish that Tacrolimus caused the reported reaction and cannot be used to estimate how often it occurs.
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