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Somatropin reports
Browse community reports connected to Somatropin. These reports can show that other people are describing similar experiences, but they do not prove that Somatropin 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.
23 problems
Abdominal Pain Upper while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and abdominal pain upper appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and abdominal pain appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and anxiety appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and back pain appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and cough appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and decreased appetite appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and diarrhea appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and dizziness appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and fatigue appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and feeling abnormal appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and headache appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and insomnia appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and malaise appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and migraine appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and nausea appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and pain appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and rash appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and shortness of breath appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and sleepiness appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and vomiting appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and weakness appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and weight decreased appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Somatropin
FDA FAERS contains adverse-event reports in which Somatropin and weight increased appear together. This does not establish that Somatropin caused the reported reaction and cannot be used to estimate how often it occurs.
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