Does SOMATROPIN Cause Intentional product use issue? 214 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 214 reports of Intentional product use issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 0.3% of all adverse event reports for SOMATROPIN.
214
Reports of Intentional product use issue with SOMATROPIN
0.3%
of all SOMATROPIN reports
6
Deaths
32
Hospitalizations
How Dangerous Is Intentional product use issue From SOMATROPIN?
Of the 214 reports, 6 (2.8%) resulted in death, 32 (15.0%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 214 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 use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which SOMATROPIN Alternatives Have Lower Intentional product use issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL