Does ETONOGESTREL Cause Product prescribing issue? 311 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 311 reports of Product prescribing issue have been filed in association with ETONOGESTREL (Nexplanon). This represents 0.7% of all adverse event reports for ETONOGESTREL.
311
Reports of Product prescribing issue with ETONOGESTREL
0.7%
of all ETONOGESTREL reports
0
Deaths
10
Hospitalizations
How Dangerous Is Product prescribing issue From ETONOGESTREL?
Of the 311 reports, 10 (3.2%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 311 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
MORPHINE (288)
Which ETONOGESTREL Alternatives Have Lower Product prescribing issue Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL