Does LEVONORGESTREL Cause Complication associated with device? 344 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 344 reports of Complication associated with device have been filed in association with LEVONORGESTREL (Mirena). This represents 0.3% of all adverse event reports for LEVONORGESTREL.
344
Reports of Complication associated with device with LEVONORGESTREL
0.3%
of all LEVONORGESTREL reports
3
Deaths
88
Hospitalizations
How Dangerous Is Complication associated with device From LEVONORGESTREL?
Of the 344 reports, 3 (0.9%) resulted in death, 88 (25.6%) required hospitalization, and 31 (9.0%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVONORGESTREL. However, 344 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
AMBRISENTAN (125)
Which LEVONORGESTREL Alternatives Have Lower Complication associated with device Risk?
LEVONORGESTREL vs LEVORPHANOL
LEVONORGESTREL vs LEVOSIMENDAN
LEVONORGESTREL vs LEVOSULPIRIDE
LEVONORGESTREL vs LEVOTHYROXINE
LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE