Does ETONOGESTREL Cause Complication associated with device? 6,047 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6,047 reports of Complication associated with device have been filed in association with ETONOGESTREL (Nexplanon). This represents 13.6% of all adverse event reports for ETONOGESTREL.
6,047
Reports of Complication associated with device with ETONOGESTREL
13.6%
of all ETONOGESTREL reports
3
Deaths
199
Hospitalizations
How Dangerous Is Complication associated with device From ETONOGESTREL?
Of the 6,047 reports, 3 (0.0%) resulted in death, 199 (3.3%) required hospitalization, and 25 (0.4%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 6,047 reports have been filed with the FAERS database.
What Other Side Effects Does ETONOGESTREL Cause?
No adverse event (8,827)
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)
Complication of device insertion (3,234)
What Other Drugs Cause Complication associated with device?
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
AMBRISENTAN (125)
Which ETONOGESTREL Alternatives Have Lower Complication associated with device Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL