Does LEVONORGESTREL Cause Device use error? 522 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 522 reports of Device use error have been filed in association with LEVONORGESTREL (Mirena). This represents 0.5% of all adverse event reports for LEVONORGESTREL.
522
Reports of Device use error with LEVONORGESTREL
0.5%
of all LEVONORGESTREL reports
0
Deaths
173
Hospitalizations
How Dangerous Is Device use error From LEVONORGESTREL?
Of the 522 reports, 173 (33.1%) required hospitalization, and 24 (4.6%) were considered life-threatening.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVONORGESTREL. However, 522 reports have been filed with the FAERS database.
What Other Side Effects Does LEVONORGESTREL Cause?
Device expulsion (27,572)
Device dislocation (13,757)
Vaginal haemorrhage (10,910)
Genital haemorrhage (7,968)
Drug ineffective (6,008)
Abdominal pain lower (5,938)
Procedural pain (5,572)
Uterine perforation (4,973)
Nausea (4,879)
Complication of device insertion (4,662)
What Other Drugs Cause Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which LEVONORGESTREL Alternatives Have Lower Device use error Risk?
LEVONORGESTREL vs LEVORPHANOL
LEVONORGESTREL vs LEVOSIMENDAN
LEVONORGESTREL vs LEVOSULPIRIDE
LEVONORGESTREL vs LEVOTHYROXINE
LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE