Does SOMATROPIN Cause Device occlusion? 823 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 823 reports of Device occlusion have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 1.2% of all adverse event reports for SOMATROPIN.
823
Reports of Device occlusion with SOMATROPIN
1.2%
of all SOMATROPIN reports
1
Deaths
11
Hospitalizations
How Dangerous Is Device occlusion From SOMATROPIN?
Of the 823 reports, 1 (0.1%) resulted in death, 11 (1.3%) required hospitalization, and 2 (0.2%) were considered life-threatening.
Is Device occlusion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 823 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 occlusion?
PEGFILGRASTIM (3,239)
CARBIDOPA\LEVODOPA (1,464)
LEUPROLIDE (786)
EPOPROSTENOL (580)
TREPROSTINIL (458)
ALBUTEROL (431)
MEDROXYPROGESTERONE (284)
BACLOFEN (254)
LEVODOPA (224)
RISPERIDONE (182)
Which SOMATROPIN Alternatives Have Lower Device occlusion Risk?
SOMATROPIN vs SONIDEGIB
SOMATROPIN vs SORAFENIB
SOMATROPIN vs SORGHUM HALEPENSE POLLEN
SOMATROPIN vs SOTAGLIFLOZIN
SOMATROPIN vs SOTALOL