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Antacid reports

Browse community reports connected to Antacid. These reports can show that other people are describing similar experiences, but they do not prove that Antacid 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.

33 problems

Abdominal Discomfort while using Antacid

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

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Abdominal Pain Upper while using Antacid

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

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Abdominal Pain while using Antacid

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

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Acid reflux while using Antacid

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

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Alopecia while using Antacid

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

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Anxiety while using Antacid

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

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Constipation while using Antacid

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

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Cough while using Antacid

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

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Decreased Appetite while using Antacid

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

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Diarrhea while using Antacid

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

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Dizziness while using Antacid

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

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Dry Mouth while using Antacid

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

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Dyspepsia while using Antacid

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

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Fatigue while using Antacid

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

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Headache while using Antacid

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

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Hives while using Antacid

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

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Insomnia while using Antacid

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

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Itching while using Antacid

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

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Malaise while using Antacid

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

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Muscle Spasms while using Antacid

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

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Muscular Weakness while using Antacid

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

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Nausea while using Antacid

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

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Pain while using Antacid

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

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Peripheral swelling while using Antacid

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

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Rash while using Antacid

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

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Shortness of breath while using Antacid

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

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Sleep Disorder while using Antacid

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

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Swelling while using Antacid

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

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

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Vomiting while using Antacid

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

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Weakness while using Antacid

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

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Weight Decreased while using Antacid

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

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Weight Increased while using Antacid

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

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