Does SOMATROPIN Cause Device power source issue? 1,219 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,219 reports of Device power source issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 1.8% of all adverse event reports for SOMATROPIN.
1,219
Reports of Device power source issue with SOMATROPIN
1.8%
of all SOMATROPIN reports
1
Deaths
3
Hospitalizations
How Dangerous Is Device power source issue From SOMATROPIN?
Of the 1,219 reports, 1 (0.1%) resulted in death, 3 (0.2%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device power source issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 1,219 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 power source issue?
PEGFILGRASTIM (486)
TREPROSTINIL (299)
CARBIDOPA\LEVODOPA (62)
ETANERCEPT (54)
BACLOFEN (50)
GLYCOPYRROLATE (39)
DEVICE (20)
FOSCARBIDOPA\FOSLEVODOPA (14)
INTERFERON BETA-1B (13)
LECITHIN\POLOXAMER 407 (11)
Which SOMATROPIN Alternatives Have Lower Device power source issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL