Does SOMATROPIN Cause Device mechanical issue? 6,411 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6,411 reports of Device mechanical issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 9.4% of all adverse event reports for SOMATROPIN.
6,411
Reports of Device mechanical issue with SOMATROPIN
9.4%
of all SOMATROPIN reports
1
Deaths
28
Hospitalizations
How Dangerous Is Device mechanical issue From SOMATROPIN?
Of the 6,411 reports, 1 (0.0%) resulted in death, 28 (0.4%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Device mechanical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 6,411 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 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 mechanical issue?
INSULIN GLARGINE-YFGN (853)
INSULIN GLARGINE (725)
ALBUTEROL (455)
DEVICE (226)
ETANERCEPT (145)
FLUTICASONE\SALMETEROL (127)
GLATIRAMER (124)
EXENATIDE (108)
MEDROXYPROGESTERONE (99)
ADALIMUMAB-AFZB (76)
Which SOMATROPIN Alternatives Have Lower Device mechanical issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL