The most commonly reported side effects of somatropin include drug dose omission by device, device leakage, and device breakage, based on 83,274 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for somatropin.
These are voluntary reports and do not establish that somatropin caused these reactions.
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Other drugs that appear in adverse event reports alongside somatropin. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
37.3% of somatropin adverse event reports involve female patients and 55.3% involve male patients. The largest age group is adolescent at 39%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking somatropin when the adverse event was reported.
Showing 15 of 1,153 indications
Somatropin is sold under brand names including Accretropin, Zorbtive, Nutropin.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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