Does LEVONORGESTREL Cause Device issue? 2,623 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,623 reports of Device issue have been filed in association with LEVONORGESTREL (Mirena). This represents 2.3% of all adverse event reports for LEVONORGESTREL.
2,623
Reports of Device issue with LEVONORGESTREL
2.3%
of all LEVONORGESTREL reports
1
Deaths
1,341
Hospitalizations
How Dangerous Is Device issue From LEVONORGESTREL?
Of the 2,623 reports, 1 (0.0%) resulted in death, 1,341 (51.1%) required hospitalization, and 203 (7.7%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVONORGESTREL. However, 2,623 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
EVOLOCUMAB (1,659)
Which LEVONORGESTREL Alternatives Have Lower Device issue Risk?
LEVONORGESTREL vs LEVORPHANOL
LEVONORGESTREL vs LEVOSIMENDAN
LEVONORGESTREL vs LEVOSULPIRIDE
LEVONORGESTREL vs LEVOTHYROXINE
LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE