Does SOMATROPIN Cause Wrong technique in product usage process? 998 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 998 reports of Wrong technique in product usage process have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 1.5% of all adverse event reports for SOMATROPIN.
998
Reports of Wrong technique in product usage process with SOMATROPIN
1.5%
of all SOMATROPIN reports
0
Deaths
34
Hospitalizations
How Dangerous Is Wrong technique in product usage process From SOMATROPIN?
Of the 998 reports, 34 (3.4%) required hospitalization, and 2 (0.2%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 998 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which SOMATROPIN Alternatives Have Lower Wrong technique in product usage process Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL