Does ETONOGESTREL Cause Device breakage? 4,140 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,140 reports of Device breakage have been filed in association with ETONOGESTREL (Nexplanon). This represents 9.3% of all adverse event reports for ETONOGESTREL.
4,140
Reports of Device breakage with ETONOGESTREL
9.3%
of all ETONOGESTREL reports
0
Deaths
44
Hospitalizations
How Dangerous Is Device breakage From ETONOGESTREL?
Of the 4,140 reports, 44 (1.1%) required hospitalization, and 4 (0.1%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 4,140 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)
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 Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
INSULIN GLARGINE (237)
Which ETONOGESTREL Alternatives Have Lower Device breakage Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL