Does ETONOGESTREL Cause Device deployment issue? 3,621 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,621 reports of Device deployment issue have been filed in association with ETONOGESTREL (Nexplanon). This represents 8.1% of all adverse event reports for ETONOGESTREL.
3,621
Reports of Device deployment issue with ETONOGESTREL
8.1%
of all ETONOGESTREL reports
0
Deaths
85
Hospitalizations
How Dangerous Is Device deployment issue From ETONOGESTREL?
Of the 3,621 reports, 85 (2.3%) required hospitalization, and 10 (0.3%) were considered life-threatening.
Is Device deployment issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 3,621 reports have been filed with the FAERS database.
What Other Side Effects Does ETONOGESTREL Cause?
No adverse event (8,827)
Complication associated with device (6,047)
Product quality issue (4,651)
Device breakage (4,140)
Incorrect product administration duration (3,974)
Device difficult to use (3,799)
Unintended pregnancy (3,707)
Pregnancy with implant contraceptive (3,587)
Complication of device removal (3,578)
Complication of device insertion (3,234)
What Other Drugs Cause Device deployment issue?
GOLIMUMAB (1,265)
GUSELKUMAB (778)
COPPER (768)
LEVONORGESTREL (718)
USTEKINUMAB (639)
SUMATRIPTAN (292)
PEGFILGRASTIM (163)
ABATACEPT (131)
SOMATROPIN (130)
CARBIDOPA\LEVODOPA (88)
Which ETONOGESTREL Alternatives Have Lower Device deployment issue Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL