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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does LEVONORGESTREL Cause Product administration error? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product administration error have been filed in association with LEVONORGESTREL (Mirena). This represents 0.0% of all adverse event reports for LEVONORGESTREL.

11
Reports of Product administration error with LEVONORGESTREL
0.0%
of all LEVONORGESTREL reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product administration error From LEVONORGESTREL?

Of the 11 reports.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LEVONORGESTREL. However, 11 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 Product administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which LEVONORGESTREL Alternatives Have Lower Product administration error Risk?

LEVONORGESTREL vs LEVORPHANOL LEVONORGESTREL vs LEVOSIMENDAN LEVONORGESTREL vs LEVOSULPIRIDE LEVONORGESTREL vs LEVOTHYROXINE LEVONORGESTREL vs LEVOTHYROXINE\LEVOTHYROXINE

Related Pages

LEVONORGESTREL Full Profile All Product administration error Reports All Drugs Causing Product administration error LEVONORGESTREL Demographics