Does SOMATROPIN Cause Product dose omission issue? 2,035 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,035 reports of Product dose omission issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 3.0% of all adverse event reports for SOMATROPIN.
2,035
Reports of Product dose omission issue with SOMATROPIN
3.0%
of all SOMATROPIN reports
14
Deaths
210
Hospitalizations
How Dangerous Is Product dose omission issue From SOMATROPIN?
Of the 2,035 reports, 14 (0.7%) resulted in death, 210 (10.3%) required hospitalization, and 9 (0.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 2,035 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which SOMATROPIN Alternatives Have Lower Product dose omission issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL