Does LEVOTHYROXINE Cause Product quality issue? 694 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 694 reports of Product quality issue have been filed in association with LEVOTHYROXINE (LEVOTHYROXINE SODIUM). This represents 1.1% of all adverse event reports for LEVOTHYROXINE.
694
Reports of Product quality issue with LEVOTHYROXINE
1.1%
of all LEVOTHYROXINE reports
0
Deaths
30
Hospitalizations
How Dangerous Is Product quality issue From LEVOTHYROXINE?
Of the 694 reports, 30 (4.3%) required hospitalization, and 14 (2.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOTHYROXINE. However, 694 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which LEVOTHYROXINE Alternatives Have Lower Product quality issue Risk?
LEVOTHYROXINE vs LEVOTHYROXINE\LEVOTHYROXINE
LEVOTHYROXINE vs LEVOTHYROXINE\LIOTHYRONINE
LEVOTHYROXINE vs LEVOXYL
LEVOTHYROXINE vs LEXAPRO
LEVOTHYROXINE vs LEXISCAN