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