Does LEVOTHYROXINE Cause Suspected product quality issue? 37 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Suspected product quality issue have been filed in association with LEVOTHYROXINE (LEVOTHYROXINE SODIUM). This represents 0.1% of all adverse event reports for LEVOTHYROXINE.
37
Reports of Suspected product quality issue with LEVOTHYROXINE
0.1%
of all LEVOTHYROXINE reports
0
Deaths
8
Hospitalizations
How Dangerous Is Suspected product quality issue From LEVOTHYROXINE?
Of the 37 reports, 8 (21.6%) required hospitalization, and 1 (2.7%) were considered life-threatening.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOTHYROXINE. However, 37 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 Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
PROPOFOL (25)
Which LEVOTHYROXINE Alternatives Have Lower Suspected product quality issue Risk?
LEVOTHYROXINE vs LEVOTHYROXINE\LEVOTHYROXINE
LEVOTHYROXINE vs LEVOTHYROXINE\LIOTHYRONINE
LEVOTHYROXINE vs LEVOXYL
LEVOTHYROXINE vs LEXAPRO
LEVOTHYROXINE vs LEXISCAN