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Pantoprazole Sodium in 0.9% Sodium Chloride reports
Browse community reports connected to Pantoprazole Sodium in 0.9% Sodium Chloride. These reports can show that other people are describing similar experiences, but they do not prove that Pantoprazole Sodium in 0.9% Sodium Chloride 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 in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and abdominal discomfort appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride 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 in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and abdominal pain upper appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and abdominal pain appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and alopecia appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and anxiety appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and back pain appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and constipation appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and cough appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and decreased appetite appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and diarrhea appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and dizziness appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and dyspepsia appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and fatigue appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and headache appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and hives appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and hypotension appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and insomnia appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and itching appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and malaise appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and muscle spasms appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and nausea appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and pain appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and peripheral swelling appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and rash appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride 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 in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and shortness of breath appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and sleep disorder appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and swelling appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride 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 in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and tingling or pins and needles appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and vomiting appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and weakness appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and weight decreased appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Pantoprazole Sodium in 0.9% Sodium Chloride
FDA FAERS contains adverse-event reports in which Pantoprazole Sodium in 0.9% Sodium Chloride and weight increased appear together. This does not establish that Pantoprazole Sodium in 0.9% Sodium Chloride caused the reported reaction and cannot be used to estimate how often it occurs.
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