Does LEVOTHYROXINE Cause Wrong patient received product? 102 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 102 reports of Wrong patient received product have been filed in association with LEVOTHYROXINE (LEVOTHYROXINE SODIUM). This represents 0.2% of all adverse event reports for LEVOTHYROXINE.
102
Reports of Wrong patient received product with LEVOTHYROXINE
0.2%
of all LEVOTHYROXINE reports
23
Deaths
60
Hospitalizations
How Dangerous Is Wrong patient received product From LEVOTHYROXINE?
Of the 102 reports, 23 (22.5%) resulted in death, 60 (58.8%) required hospitalization, and 7 (6.9%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOTHYROXINE. However, 102 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 Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which LEVOTHYROXINE Alternatives Have Lower Wrong patient received product Risk?
LEVOTHYROXINE vs LEVOTHYROXINE\LEVOTHYROXINE
LEVOTHYROXINE vs LEVOTHYROXINE\LIOTHYRONINE
LEVOTHYROXINE vs LEVOXYL
LEVOTHYROXINE vs LEXAPRO
LEVOTHYROXINE vs LEXISCAN