Does LEVOTHYROXINE\LIOTHYRONINE Cause Recalled product administered? 108 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 108 reports of Recalled product administered have been filed in association with LEVOTHYROXINE\LIOTHYRONINE. This represents 11.5% of all adverse event reports for LEVOTHYROXINE\LIOTHYRONINE.
108
Reports of Recalled product administered with LEVOTHYROXINE\LIOTHYRONINE
11.5%
of all LEVOTHYROXINE\LIOTHYRONINE reports
3
Deaths
13
Hospitalizations
How Dangerous Is Recalled product administered From LEVOTHYROXINE\LIOTHYRONINE?
Of the 108 reports, 3 (2.8%) resulted in death, 13 (12.0%) required hospitalization, and 11 (10.2%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVOTHYROXINE\LIOTHYRONINE. However, 108 reports have been filed with the FAERS database.
What Other Side Effects Does LEVOTHYROXINE\LIOTHYRONINE Cause?
Fatigue (261)
Palpitations (145)
Heart rate increased (117)
Alopecia (116)
Weight increased (101)
Feeling abnormal (99)
Dizziness (91)
Headache (90)
Anxiety (81)
Product odour abnormal (77)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which LEVOTHYROXINE\LIOTHYRONINE Alternatives Have Lower Recalled product administered Risk?
LEVOTHYROXINE\LIOTHYRONINE vs LEVOXYL
LEVOTHYROXINE\LIOTHYRONINE vs LEXAPRO
LEVOTHYROXINE\LIOTHYRONINE vs LEXISCAN
LEVOTHYROXINE\LIOTHYRONINE vs LIALDA
LEVOTHYROXINE\LIOTHYRONINE vs LIDOCAINE