Does LEVOTHYROXINE Cause Product administration error? 104 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 104 reports of Product administration error have been filed in association with LEVOTHYROXINE (LEVOTHYROXINE SODIUM). This represents 0.2% of all adverse event reports for LEVOTHYROXINE.
104
Reports of Product administration error with LEVOTHYROXINE
0.2%
of all LEVOTHYROXINE reports
10
Deaths
46
Hospitalizations
How Dangerous Is Product administration error From LEVOTHYROXINE?
Of the 104 reports, 10 (9.6%) resulted in death, 46 (44.2%) required hospitalization, and 5 (4.8%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOTHYROXINE. However, 104 reports have been filed with the FAERS database.
What Other Side Effects Does LEVOTHYROXINE Cause?
Fatigue (10,494)
Headache (6,425)
Insomnia (4,663)
Drug ineffective (4,556)
Alopecia (4,491)
Weight increased (4,130)
Nausea (4,013)
Palpitations (3,825)
Dizziness (3,761)
Asthenia (3,694)
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 LEVOTHYROXINE Alternatives Have Lower Product administration error Risk?
LEVOTHYROXINE vs LEVOTHYROXINE\LEVOTHYROXINE
LEVOTHYROXINE vs LEVOTHYROXINE\LIOTHYRONINE
LEVOTHYROXINE vs LEVOXYL
LEVOTHYROXINE vs LEXAPRO
LEVOTHYROXINE vs LEXISCAN