Does PYRIDOXINE\THIAMINE Cause Incorrect product administration duration? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect product administration duration have been filed in association with PYRIDOXINE\THIAMINE. This represents 5.4% of all adverse event reports for PYRIDOXINE\THIAMINE.
7
Reports of Incorrect product administration duration with PYRIDOXINE\THIAMINE
5.4%
of all PYRIDOXINE\THIAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From PYRIDOXINE\THIAMINE?
Of the 7 reports, and 7 (100.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PYRIDOXINE\THIAMINE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does PYRIDOXINE\THIAMINE Cause?
Back pain (28)
Head discomfort (28)
Migraine (28)
Neck pain (28)
Pain (28)
Headache (27)
Acute kidney injury (15)
Lactic acidosis (14)
Thrombocytopenia (14)
Hepatocellular injury (13)
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 PYRIDOXINE\THIAMINE Alternatives Have Lower Incorrect product administration duration Risk?
PYRIDOXINE\THIAMINE vs PYRIMETHAMINE
PYRIDOXINE\THIAMINE vs PYROTINIB
PYRIDOXINE\THIAMINE vs QSYMIA
PYRIDOXINE\THIAMINE vs QUETIAPINE
PYRIDOXINE\THIAMINE vs QUINACRINE