Does SOMATROPIN Cause Device breakage? 7,761 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7,761 reports of Device breakage have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 11.4% of all adverse event reports for SOMATROPIN.
7,761
Reports of Device breakage with SOMATROPIN
11.4%
of all SOMATROPIN reports
2
Deaths
54
Hospitalizations
How Dangerous Is Device breakage From SOMATROPIN?
Of the 7,761 reports, 2 (0.0%) resulted in death, 54 (0.7%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 7,761 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 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)
Incorrect dose administered (2,772)
What Other Drugs Cause Device breakage?
COPPER (9,201)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
INSULIN GLARGINE (237)
Which SOMATROPIN Alternatives Have Lower Device breakage Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL