Does LEVONORGESTREL Cause Device defective? 293 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 293 reports of Device defective have been filed in association with LEVONORGESTREL (Mirena). This represents 0.3% of all adverse event reports for LEVONORGESTREL.
293
Reports of Device defective with LEVONORGESTREL
0.3%
of all LEVONORGESTREL reports
0
Deaths
72
Hospitalizations
How Dangerous Is Device defective From LEVONORGESTREL?
Of the 293 reports, 72 (24.6%) required hospitalization, and 28 (9.6%) were considered life-threatening.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVONORGESTREL. However, 293 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 defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which LEVONORGESTREL Alternatives Have Lower Device defective Risk?
LEVONORGESTREL vs LEVORPHANOL
LEVONORGESTREL vs LEVOSIMENDAN
LEVONORGESTREL vs LEVOSULPIRIDE
LEVONORGESTREL vs LEVOTHYROXINE
LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE