Does SOMATROPIN Cause Product preparation error? 170 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 170 reports of Product preparation error have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 0.3% of all adverse event reports for SOMATROPIN.
170
Reports of Product preparation error with SOMATROPIN
0.3%
of all SOMATROPIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product preparation error From SOMATROPIN?
Of the 170 reports, 2 (1.2%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 170 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which SOMATROPIN Alternatives Have Lower Product preparation error Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL