Vitamin C reports

Abdominal Discomfort while using Vitamin C

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

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Abdominal Pain Upper while using Vitamin C

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

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Abdominal Pain while using Vitamin C

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

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Acid reflux while using Vitamin C

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

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Alopecia while using Vitamin C

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

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Anxiety while using Vitamin C

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

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Back Pain while using Vitamin C

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

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Constipation while using Vitamin C

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

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Cough while using Vitamin C

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

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Decreased Appetite while using Vitamin C

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

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Diarrhea while using Vitamin C

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

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Dizziness while using Vitamin C

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

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Dry Mouth while using Vitamin C

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

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Dyspepsia while using Vitamin C

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

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Fatigue while using Vitamin C

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

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Feeling Abnormal while using Vitamin C

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

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Headache while using Vitamin C

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

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Hives while using Vitamin C

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

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Insomnia while using Vitamin C

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

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Itching while using Vitamin C

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

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Malaise while using Vitamin C

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

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Migraine while using Vitamin C

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

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Muscle Spasms while using Vitamin C

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

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Muscular Weakness while using Vitamin C

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

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Nausea while using Vitamin C

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

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Night Sweats while using Vitamin C

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

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Pain while using Vitamin C

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

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Rash while using Vitamin C

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

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Shortness of breath while using Vitamin C

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

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Skin redness while using Vitamin C

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

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Sleep Disorder while using Vitamin C

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

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Sleepiness while using Vitamin C

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

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Swelling while using Vitamin C

FDA FAERS contains adverse-event reports in which Vitamin C and swelling appear together. This does not establish that Vitamin C 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 Vitamin C

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

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Vomiting while using Vitamin C

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

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Weakness while using Vitamin C

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

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Weight Decreased while using Vitamin C

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

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Weight Increased while using Vitamin C

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

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