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Teriparatide reports
Browse community reports connected to Teriparatide. These reports can show that other people are describing similar experiences, but they do not prove that Teriparatide 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.
41 problems
Abdominal Discomfort while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and abdominal discomfort appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and abdominal distension appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and abdominal pain upper appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and abdominal pain appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and alopecia appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and anxiety appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and back pain appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and constipation appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and cough appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and decreased appetite appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and dehydration appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and diarrhea appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and dizziness appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and dyspepsia appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and excessive sweating appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and fatigue appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and feeling abnormal appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and headache appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and heart rate increased appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and insomnia appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and itching appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and malaise appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and muscle spasms appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and muscular weakness appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and myalgia appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and nausea appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Neck Pain while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and neck pain appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Nervousness while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and nervousness appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and pain appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and palpitations appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and peripheral swelling appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and rash appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and shortness of breath appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and skin redness appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and sleepiness appear together. This does not establish that Teriparatide 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 Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and tingling or pins and needles appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and tremor appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and vomiting appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and weakness appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and weight decreased appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Teriparatide
FDA FAERS contains adverse-event reports in which Teriparatide and weight increased appear together. This does not establish that Teriparatide caused the reported reaction and cannot be used to estimate how often it occurs.
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