Does SOMATROPIN Cause Device use issue? 2,571 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,571 reports of Device use issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 3.8% of all adverse event reports for SOMATROPIN.
2,571
Reports of Device use issue with SOMATROPIN
3.8%
of all SOMATROPIN reports
1
Deaths
19
Hospitalizations
How Dangerous Is Device use issue From SOMATROPIN?
Of the 2,571 reports, 1 (0.0%) resulted in death, 19 (0.7%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 2,571 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 use issue?
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
LEVODOPA (443)
Which SOMATROPIN Alternatives Have Lower Device use issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL