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Pantoprazole Sodium Injection reports

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

32 problems

Abdominal Discomfort while using Pantoprazole Sodium Injection

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

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Abdominal Pain Upper while using Pantoprazole Sodium Injection

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

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Abdominal Pain while using Pantoprazole Sodium Injection

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

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Alopecia while using Pantoprazole Sodium Injection

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

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Anxiety while using Pantoprazole Sodium Injection

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

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Back Pain while using Pantoprazole Sodium Injection

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

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Constipation while using Pantoprazole Sodium Injection

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

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Cough while using Pantoprazole Sodium Injection

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

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Decreased Appetite while using Pantoprazole Sodium Injection

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

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Diarrhea while using Pantoprazole Sodium Injection

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

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Dizziness while using Pantoprazole Sodium Injection

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

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Dyspepsia while using Pantoprazole Sodium Injection

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

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Fatigue while using Pantoprazole Sodium Injection

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

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Headache while using Pantoprazole Sodium Injection

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

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Hives while using Pantoprazole Sodium Injection

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

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Hypotension while using Pantoprazole Sodium Injection

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

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Insomnia while using Pantoprazole Sodium Injection

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

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Itching while using Pantoprazole Sodium Injection

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

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Malaise while using Pantoprazole Sodium Injection

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

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Muscle Spasms while using Pantoprazole Sodium Injection

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

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Nausea while using Pantoprazole Sodium Injection

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

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Pain while using Pantoprazole Sodium Injection

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

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Peripheral swelling while using Pantoprazole Sodium Injection

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

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Rash while using Pantoprazole Sodium Injection

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

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Shortness of breath while using Pantoprazole Sodium Injection

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

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Sleep Disorder while using Pantoprazole Sodium Injection

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

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Swelling while using Pantoprazole Sodium Injection

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

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

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Vomiting while using Pantoprazole Sodium Injection

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

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Weakness while using Pantoprazole Sodium Injection

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

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Weight Decreased while using Pantoprazole Sodium Injection

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

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Weight Increased while using Pantoprazole Sodium Injection

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

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