Does SOMATROPIN Cause Product storage error? 1,098 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,098 reports of Product storage error have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 1.6% of all adverse event reports for SOMATROPIN.
1,098
Reports of Product storage error with SOMATROPIN
1.6%
of all SOMATROPIN reports
1
Deaths
48
Hospitalizations
How Dangerous Is Product storage error From SOMATROPIN?
Of the 1,098 reports, 1 (0.1%) resulted in death, 48 (4.4%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 1,098 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which SOMATROPIN Alternatives Have Lower Product storage error Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL