Does SOMATROPIN Cause Product quality issue? 372 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 372 reports of Product quality issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 0.5% of all adverse event reports for SOMATROPIN.
372
Reports of Product quality issue with SOMATROPIN
0.5%
of all SOMATROPIN reports
0
Deaths
12
Hospitalizations
How Dangerous Is Product quality issue From SOMATROPIN?
Of the 372 reports, 12 (3.2%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 372 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which SOMATROPIN Alternatives Have Lower Product quality issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL