Does ETONOGESTREL Cause Adverse event? 882 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 882 reports of Adverse event have been filed in association with ETONOGESTREL (Nexplanon). This represents 2.0% of all adverse event reports for ETONOGESTREL.
882
Reports of Adverse event with ETONOGESTREL
2.0%
of all ETONOGESTREL reports
4
Deaths
70
Hospitalizations
How Dangerous Is Adverse event From ETONOGESTREL?
Of the 882 reports, 4 (0.5%) resulted in death, 70 (7.9%) required hospitalization, and 2 (0.2%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 882 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which ETONOGESTREL Alternatives Have Lower Adverse event Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL