Does ETONOGESTREL Cause Maternal exposure timing unspecified? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Maternal exposure timing unspecified have been filed in association with ETONOGESTREL (Nexplanon). This represents 0.0% of all adverse event reports for ETONOGESTREL.
6
Reports of Maternal exposure timing unspecified with ETONOGESTREL
0.0%
of all ETONOGESTREL reports
0
Deaths
1
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From ETONOGESTREL?
Of the 6 reports, 1 (16.7%) required hospitalization, and 1 (16.7%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETONOGESTREL. However, 6 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which ETONOGESTREL Alternatives Have Lower Maternal exposure timing unspecified Risk?
ETONOGESTREL vs ETOPOSIDE
ETONOGESTREL vs ETORICOXIB
ETONOGESTREL vs ETRASIMOD ARGININE
ETONOGESTREL vs ETRAVIRINE
ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL