Does ETONOGESTREL Cause Device issue? 1,312 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,312 reports of Device issue have been filed in association with ETONOGESTREL (Nexplanon). This represents 3.0% of all adverse event reports for ETONOGESTREL.
1,312
Reports of Device issue with ETONOGESTREL
3.0%
of all ETONOGESTREL reports
0
Deaths
39
Hospitalizations
How Dangerous Is Device issue From ETONOGESTREL?
Of the 1,312 reports, 39 (3.0%) required hospitalization, and 7 (0.5%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 1,312 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ETONOGESTREL Alternatives Have Lower Device issue Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL