Simvastatin reports

Abdominal Discomfort while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and abdominal discomfort appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Distension while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and abdominal distension appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain Upper while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and abdominal pain upper appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and abdominal pain appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Acid reflux while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and acid reflux appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Alopecia while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and alopecia appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and anxiety appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and back pain appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Chills while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and chills appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and constipation appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and cough appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and decreased appetite appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and dehydration appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and diarrhea appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and dizziness appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dry Mouth while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and dry mouth appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dyspepsia while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and dyspepsia appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and excessive sweating appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and fatigue appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and feeling abnormal appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Flushing while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and flushing appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and headache appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and hypotension appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and insomnia appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and itching appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and malaise appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and muscle spasms appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscular Weakness while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and muscular weakness appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Myalgia while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and myalgia appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and nausea appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and pain appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Palpitations while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and palpitations appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and peripheral swelling appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and rash appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and shortness of breath appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and skin redness appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and sleepiness appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Tachycardia while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and tachycardia appear together. This does not establish that Simvastatin 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 Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and tingling or pins and needles appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and tremor appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Vision Blurred while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and vision blurred appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and vomiting appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and weakness appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and weight decreased appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Increased while using Simvastatin

FDA FAERS contains adverse-event reports in which Simvastatin and weight increased appear together. This does not establish that Simvastatin caused the reported reaction and cannot be used to estimate how often it occurs.

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