Does SOMATROPIN Cause Intentional product misuse? 350 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 350 reports of Intentional product misuse have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 0.5% of all adverse event reports for SOMATROPIN.
350
Reports of Intentional product misuse with SOMATROPIN
0.5%
of all SOMATROPIN reports
11
Deaths
35
Hospitalizations
How Dangerous Is Intentional product misuse From SOMATROPIN?
Of the 350 reports, 11 (3.1%) resulted in death, 35 (10.0%) required hospitalization, and 8 (2.3%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 350 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which SOMATROPIN Alternatives Have Lower Intentional product misuse Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL