Does ETONOGESTREL Cause Device dislocation? 2,909 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,909 reports of Device dislocation have been filed in association with ETONOGESTREL (Nexplanon). This represents 6.5% of all adverse event reports for ETONOGESTREL.
2,909
Reports of Device dislocation with ETONOGESTREL
6.5%
of all ETONOGESTREL reports
3
Deaths
131
Hospitalizations
How Dangerous Is Device dislocation From ETONOGESTREL?
Of the 2,909 reports, 3 (0.1%) resulted in death, 131 (4.5%) required hospitalization, and 23 (0.8%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 2,909 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)
Device deployment issue (3,621)
Pregnancy with implant contraceptive (3,587)
Complication of device removal (3,578)
What Other Drugs Cause Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
DEXAMETHASONE (290)
Which ETONOGESTREL Alternatives Have Lower Device dislocation Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL