Does SOMATROPIN Cause Device information output issue? 5,220 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,220 reports of Device information output issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 7.6% of all adverse event reports for SOMATROPIN.
5,220
Reports of Device information output issue with SOMATROPIN
7.6%
of all SOMATROPIN reports
1
Deaths
16
Hospitalizations
How Dangerous Is Device information output issue From SOMATROPIN?
Of the 5,220 reports, 1 (0.0%) resulted in death, 16 (0.3%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Device information output issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 5,220 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 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 information output issue?
ALBUTEROL (318)
TREPROSTINIL (141)
CARBIDOPA\LEVODOPA (14)
INSULIN ASPART (10)
DEVICE (9)
BUDESONIDE\FORMOTEROL (7)
ETANERCEPT (7)
NOREPINEPHRINE (6)
BACLOFEN (5)
ESTRADIOL (5)
Which SOMATROPIN Alternatives Have Lower Device information output issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL