Does LIOTHYRONINE Cause Incorrect product administration duration? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Incorrect product administration duration have been filed in association with LIOTHYRONINE (Liothyronine Sodium). This represents 0.3% of all adverse event reports for LIOTHYRONINE.
9
Reports of Incorrect product administration duration with LIOTHYRONINE
0.3%
of all LIOTHYRONINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From LIOTHYRONINE?
Of the 9 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIOTHYRONINE. However, 9 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which LIOTHYRONINE Alternatives Have Lower Incorrect product administration duration Risk?
LIOTHYRONINE vs LIPEGFILGRASTIM
LIOTHYRONINE vs LIPITOR
LIOTHYRONINE vs LIRAGLUTIDE
LIOTHYRONINE vs LISDEXAMFETAMINE
LIOTHYRONINE vs LISDEXAMFETAMINE DIMESYLATE