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Hydrocortisone 1% reports
Browse community reports connected to Hydrocortisone 1%. These reports can show that other people are describing similar experiences, but they do not prove that Hydrocortisone 1% 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.
34 problems
Abdominal Discomfort while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and abdominal discomfort appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and abdominal pain upper appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and abdominal pain appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and alopecia appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and anxiety appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and back pain appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and constipation appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and cough appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and decreased appetite appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and diarrhea appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and dizziness appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and dry mouth appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and dyspepsia appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and fatigue appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and headache appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and hives appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and hypotension appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and insomnia appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and itching appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and malaise appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and migraine appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and muscle spasms appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and nausea appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and pain appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and rash appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and shortness of breath appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and skin redness appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and sleep disorder appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and swelling appear together. This does not establish that Hydrocortisone 1% 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 Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and tingling or pins and needles appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and vomiting appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and weakness appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and weight decreased appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Hydrocortisone 1%
FDA FAERS contains adverse-event reports in which Hydrocortisone 1% and weight increased appear together. This does not establish that Hydrocortisone 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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