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