Does LEVONORGESTREL Cause Incorrect product administration duration? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Incorrect product administration duration have been filed in association with LEVONORGESTREL (Mirena). This represents 0.0% of all adverse event reports for LEVONORGESTREL.
12
Reports of Incorrect product administration duration with LEVONORGESTREL
0.0%
of all LEVONORGESTREL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From LEVONORGESTREL?
Of the 12 reports, 2 (16.7%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVONORGESTREL. However, 12 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which LEVONORGESTREL Alternatives Have Lower Incorrect product administration duration Risk?
LEVONORGESTREL vs LEVORPHANOL
LEVONORGESTREL vs LEVOSIMENDAN
LEVONORGESTREL vs LEVOSULPIRIDE
LEVONORGESTREL vs LEVOTHYROXINE
LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE