Does ETONOGESTREL Cause Wrong technique in product usage process? 331 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 331 reports of Wrong technique in product usage process have been filed in association with ETONOGESTREL (Nexplanon). This represents 0.7% of all adverse event reports for ETONOGESTREL.
331
Reports of Wrong technique in product usage process with ETONOGESTREL
0.7%
of all ETONOGESTREL reports
0
Deaths
12
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ETONOGESTREL?
Of the 331 reports, 12 (3.6%) required hospitalization, and 2 (0.6%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 331 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ETONOGESTREL Alternatives Have Lower Wrong technique in product usage process Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL