Does ETONOGESTREL Cause Device expulsion? 1,993 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,993 reports of Device expulsion have been filed in association with ETONOGESTREL (Nexplanon). This represents 4.5% of all adverse event reports for ETONOGESTREL.
1,993
Reports of Device expulsion with ETONOGESTREL
4.5%
of all ETONOGESTREL reports
0
Deaths
12
Hospitalizations
How Dangerous Is Device expulsion From ETONOGESTREL?
Of the 1,993 reports, 12 (0.6%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device expulsion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 1,993 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 expulsion?
LEVONORGESTREL (27,572)
COPPER (11,141)
MIRENA (1,300)
ETHINYL ESTRADIOL\ETONOGESTREL (986)
PARAGARD 380A (685)
CARBIDOPA\LEVODOPA (129)
NEXPLANON (98)
NUVARING (92)
ESTRADIOL (57)
HISTRELIN (22)
Which ETONOGESTREL Alternatives Have Lower Device expulsion Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL