Does ETONOGESTREL Cause Product quality issue? 4,651 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,651 reports of Product quality issue have been filed in association with ETONOGESTREL (Nexplanon). This represents 10.5% of all adverse event reports for ETONOGESTREL.
4,651
Reports of Product quality issue with ETONOGESTREL
10.5%
of all ETONOGESTREL reports
1
Deaths
7
Hospitalizations
How Dangerous Is Product quality issue From ETONOGESTREL?
Of the 4,651 reports, 1 (0.0%) resulted in death, 7 (0.2%) required hospitalization, and 2 (0.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 4,651 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)
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)
Complication of device insertion (3,234)
What Other Drugs Cause Product quality issue?
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
METHYLPHENIDATE (1,728)
Which ETONOGESTREL Alternatives Have Lower Product quality issue Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL