Does ETONOGESTREL Cause Product use issue? 546 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 546 reports of Product use issue have been filed in association with ETONOGESTREL (Nexplanon). This represents 1.2% of all adverse event reports for ETONOGESTREL.
546
Reports of Product use issue with ETONOGESTREL
1.2%
of all ETONOGESTREL reports
1
Deaths
21
Hospitalizations
How Dangerous Is Product use issue From ETONOGESTREL?
Of the 546 reports, 1 (0.2%) resulted in death, 21 (3.8%) required hospitalization, and 3 (0.5%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 546 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ETONOGESTREL Alternatives Have Lower Product use issue Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL