Does LEVONORGESTREL Cause Intentional product use issue? 171 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 171 reports of Intentional product use issue have been filed in association with LEVONORGESTREL (Mirena). This represents 0.2% of all adverse event reports for LEVONORGESTREL.
171
Reports of Intentional product use issue with LEVONORGESTREL
0.2%
of all LEVONORGESTREL reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From LEVONORGESTREL?
Of the 171 reports, 1 (0.6%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVONORGESTREL. However, 171 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which LEVONORGESTREL Alternatives Have Lower Intentional product use issue Risk?
LEVONORGESTREL vs LEVORPHANOL
LEVONORGESTREL vs LEVOSIMENDAN
LEVONORGESTREL vs LEVOSULPIRIDE
LEVONORGESTREL vs LEVOTHYROXINE
LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE