Does SOMATROPIN Cause Poor quality product administered? 234 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 234 reports of Poor quality product administered have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 0.3% of all adverse event reports for SOMATROPIN.
234
Reports of Poor quality product administered with SOMATROPIN
0.3%
of all SOMATROPIN reports
0
Deaths
4
Hospitalizations
How Dangerous Is Poor quality product administered From SOMATROPIN?
Of the 234 reports, 4 (1.7%) required hospitalization.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 234 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
AMINOLEVULINIC ACID (124)
Which SOMATROPIN Alternatives Have Lower Poor quality product administered Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL