Does NEXPLANON Cause Product quality issue? 383 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 383 reports of Product quality issue have been filed in association with NEXPLANON. This represents 22.1% of all adverse event reports for NEXPLANON.
383
Reports of Product quality issue with NEXPLANON
22.1%
of all NEXPLANON reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From NEXPLANON?
Of the 383 reports.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NEXPLANON. However, 383 reports have been filed with the FAERS database.
What Other Side Effects Does NEXPLANON Cause?
No adverse event (463)
Device difficult to use (425)
Device breakage (228)
Device kink (121)
Menorrhagia (119)
Unintended pregnancy (106)
Device expulsion (98)
Medical device complication (97)
Implant site pain (84)
Device deployment issue (80)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
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)
Which NEXPLANON Alternatives Have Lower Product quality issue Risk?
NEXPLANON vs NIACIN
NEXPLANON vs NIACINAMIDE
NEXPLANON vs NICARDIPINE
NEXPLANON vs NICORANDIL
NEXPLANON vs NICORETTE OTC