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