Does ETONOGESTREL Cause Medical device complication? 829 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 829 reports of Medical device complication have been filed in association with ETONOGESTREL (Nexplanon). This represents 1.9% of all adverse event reports for ETONOGESTREL.
829
Reports of Medical device complication with ETONOGESTREL
1.9%
of all ETONOGESTREL reports
1
Deaths
25
Hospitalizations
How Dangerous Is Medical device complication From ETONOGESTREL?
Of the 829 reports, 1 (0.1%) resulted in death, 25 (3.0%) required hospitalization, and 3 (0.4%) were considered life-threatening.
Is Medical device complication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 829 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 Medical device complication?
COPPER (213)
IMPLANON (190)
LEVONORGESTREL (120)
NEXPLANON (97)
TREPROSTINIL (94)
PARAGARD 380A (91)
EPOPROSTENOL (76)
AMBRISENTAN (53)
BACLOFEN (53)
RISPERIDONE (51)
Which ETONOGESTREL Alternatives Have Lower Medical device complication Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL