Does SOMATROPIN Cause Device issue? 5,131 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,131 reports of Device issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 7.5% of all adverse event reports for SOMATROPIN.
5,131
Reports of Device issue with SOMATROPIN
7.5%
of all SOMATROPIN reports
2
Deaths
69
Hospitalizations
How Dangerous Is Device issue From SOMATROPIN?
Of the 5,131 reports, 2 (0.0%) resulted in death, 69 (1.3%) required hospitalization, and 3 (0.1%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 5,131 reports have been filed with the FAERS database.
What Other Side Effects Does SOMATROPIN Cause?
Drug dose omission by device (15,921)
Device leakage (9,113)
Device breakage (7,761)
Device mechanical issue (6,411)
Device information output issue (5,220)
Wrong technique in device usage process (4,746)
Injection site pain (4,009)
Poor quality device used (3,162)
Device use error (2,801)
Incorrect dose administered (2,772)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
EVOLOCUMAB (1,659)
Which SOMATROPIN Alternatives Have Lower Device issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL