Does SOMATROPIN Cause Device failure? 1,141 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,141 reports of Device failure have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 1.7% of all adverse event reports for SOMATROPIN.
1,141
Reports of Device failure with SOMATROPIN
1.7%
of all SOMATROPIN reports
0
Deaths
10
Hospitalizations
How Dangerous Is Device failure From SOMATROPIN?
Of the 1,141 reports, 10 (0.9%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 1,141 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 failure?
EPINEPHRINE (1,344)
PEGFILGRASTIM (829)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
ACLIDINIUM (304)
INSULIN ASPART (271)
Which SOMATROPIN Alternatives Have Lower Device failure Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL