Does SOMATROPIN Cause Device leakage? 9,113 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9,113 reports of Device leakage have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 13.3% of all adverse event reports for SOMATROPIN.
9,113
Reports of Device leakage with SOMATROPIN
13.3%
of all SOMATROPIN reports
3
Deaths
51
Hospitalizations
How Dangerous Is Device leakage From SOMATROPIN?
Of the 9,113 reports, 3 (0.0%) resulted in death, 51 (0.6%) required hospitalization, and 3 (0.0%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 9,113 reports have been filed with the FAERS database.
What Other Side Effects Does SOMATROPIN Cause?
Drug dose omission by device (15,921)
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)
Incorrect dose administered (2,772)
What Other Drugs Cause Device leakage?
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
ABATACEPT (671)
Which SOMATROPIN Alternatives Have Lower Device leakage Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL