Does LIOTHYRONINE Cause Recalled product administered? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Recalled product administered have been filed in association with LIOTHYRONINE (Liothyronine Sodium). This represents 1.1% of all adverse event reports for LIOTHYRONINE.
30
Reports of Recalled product administered with LIOTHYRONINE
1.1%
of all LIOTHYRONINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From LIOTHYRONINE?
Of the 30 reports.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIOTHYRONINE. However, 30 reports have been filed with the FAERS database.
What Other Side Effects Does LIOTHYRONINE Cause?
Drug ineffective (505)
Headache (381)
Hypothyroidism (321)
Hypertension (295)
Dyspnoea (285)
Therapeutic product effect incomplete (283)
Cardiac disorder (269)
Asthma (257)
Burning sensation (257)
Gastrooesophageal reflux disease (257)
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 LIOTHYRONINE Alternatives Have Lower Recalled product administered Risk?
LIOTHYRONINE vs LIPEGFILGRASTIM
LIOTHYRONINE vs LIPITOR
LIOTHYRONINE vs LIRAGLUTIDE
LIOTHYRONINE vs LISDEXAMFETAMINE
LIOTHYRONINE vs LISDEXAMFETAMINE DIMESYLATE