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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ETONOGESTREL Cause Device failure? 30 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Device failure have been filed in association with ETONOGESTREL (Nexplanon). This represents 0.1% of all adverse event reports for ETONOGESTREL.

30
Reports of Device failure with ETONOGESTREL
0.1%
of all ETONOGESTREL reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device failure From ETONOGESTREL?

Of the 30 reports, and 1 (3.3%) were considered life-threatening.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 30 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 failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Which ETONOGESTREL Alternatives Have Lower Device failure Risk?

ETONOGESTREL vs ETOPOSIDE ETONOGESTREL vs ETORICOXIB ETONOGESTREL vs ETRASIMOD ARGININE ETONOGESTREL vs ETRAVIRINE ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL

Related Pages

ETONOGESTREL Full Profile All Device failure Reports All Drugs Causing Device failure ETONOGESTREL Demographics