Does SOMATROPIN Cause Device material issue? 472 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 472 reports of Device material issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 0.7% of all adverse event reports for SOMATROPIN.
472
Reports of Device material issue with SOMATROPIN
0.7%
of all SOMATROPIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device material issue From SOMATROPIN?
Of the 472 reports, 1 (0.2%) required hospitalization.
Is Device material issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 472 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 material issue?
COPPER (603)
CARBIDOPA\LEVODOPA (68)
ADALIMUMAB (62)
ESTRADIOL (51)
PEGFILGRASTIM (33)
ESTRADIOL\LEVONORGESTREL (24)
ABATACEPT (14)
LEVONORGESTREL (13)
BACLOFEN (11)
METHOTREXATE (9)
Which SOMATROPIN Alternatives Have Lower Device material issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL