Does SOMATROPIN Cause Device use error? 2,801 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,801 reports of Device use error have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 4.1% of all adverse event reports for SOMATROPIN.
2,801
Reports of Device use error with SOMATROPIN
4.1%
of all SOMATROPIN reports
1
Deaths
15
Hospitalizations
How Dangerous Is Device use error From SOMATROPIN?
Of the 2,801 reports, 1 (0.0%) resulted in death, 15 (0.5%) required hospitalization.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 2,801 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)
Incorrect dose administered (2,772)
What Other Drugs Cause Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
TREPROSTINIL (563)
Which SOMATROPIN Alternatives Have Lower Device use error Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL