Does SOMATROPIN Cause Device delivery system issue? 1,848 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,848 reports of Device delivery system issue have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 2.7% of all adverse event reports for SOMATROPIN.
1,848
Reports of Device delivery system issue with SOMATROPIN
2.7%
of all SOMATROPIN reports
0
Deaths
10
Hospitalizations
How Dangerous Is Device delivery system issue From SOMATROPIN?
Of the 1,848 reports, 10 (0.5%) required hospitalization.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 1,848 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 Device delivery system issue?
ALBUTEROL (9,509)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
ALBUTEROL\BUDESONIDE (244)
Which SOMATROPIN Alternatives Have Lower Device delivery system issue Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL