Does LEVOTHYROXINE Cause Recalled product administered? 406 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 406 reports of Recalled product administered have been filed in association with LEVOTHYROXINE (LEVOTHYROXINE SODIUM). This represents 0.7% of all adverse event reports for LEVOTHYROXINE.
406
Reports of Recalled product administered with LEVOTHYROXINE
0.7%
of all LEVOTHYROXINE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Recalled product administered From LEVOTHYROXINE?
Of the 406 reports, 4 (1.0%) required hospitalization.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOTHYROXINE. However, 406 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
LOSARTAN (141)
Which LEVOTHYROXINE Alternatives Have Lower Recalled product administered Risk?
LEVOTHYROXINE vs LEVOTHYROXINE\LEVOTHYROXINE
LEVOTHYROXINE vs LEVOTHYROXINE\LIOTHYRONINE
LEVOTHYROXINE vs LEVOXYL
LEVOTHYROXINE vs LEXAPRO
LEVOTHYROXINE vs LEXISCAN