Does LEVOTHYROXINE Cause Recalled product? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Recalled product have been filed in association with LEVOTHYROXINE (LEVOTHYROXINE SODIUM). This represents 0.0% of all adverse event reports for LEVOTHYROXINE.
24
Reports of Recalled product with LEVOTHYROXINE
0.0%
of all LEVOTHYROXINE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Recalled product From LEVOTHYROXINE?
Of the 24 reports, 1 (4.2%) resulted in death, 2 (8.3%) required hospitalization.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOTHYROXINE. However, 24 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?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which LEVOTHYROXINE Alternatives Have Lower Recalled product Risk?
LEVOTHYROXINE vs LEVOTHYROXINE\LEVOTHYROXINE
LEVOTHYROXINE vs LEVOTHYROXINE\LIOTHYRONINE
LEVOTHYROXINE vs LEVOXYL
LEVOTHYROXINE vs LEXAPRO
LEVOTHYROXINE vs LEXISCAN