Does SOMATROPIN Cause Device defective? 1,719 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,719 reports of Device defective have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 2.5% of all adverse event reports for SOMATROPIN.
1,719
Reports of Device defective with SOMATROPIN
2.5%
of all SOMATROPIN reports
1
Deaths
8
Hospitalizations
How Dangerous Is Device defective From SOMATROPIN?
Of the 1,719 reports, 1 (0.1%) resulted in death, 8 (0.5%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 1,719 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)
Device issue (5,131)
Wrong technique in device usage process (4,746)
Injection site pain (4,009)
Poor quality device used (3,162)
Device use error (2,801)
What Other Drugs Cause Device defective?
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
BUDESONIDE\FORMOTEROL (378)
Which SOMATROPIN Alternatives Have Lower Device defective Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL