Does SOMATROPIN Cause Product use issue? 246 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 246 reports of Product use issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 0.4% of all adverse event reports for SOMATROPIN.
246
Reports of Product use issue with SOMATROPIN
0.4%
of all SOMATROPIN reports
11
Deaths
38
Hospitalizations
How Dangerous Is Product use issue From SOMATROPIN?
Of the 246 reports, 11 (4.5%) resulted in death, 38 (15.4%) required hospitalization, and 3 (1.2%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 246 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which SOMATROPIN Alternatives Have Lower Product use issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL