Does TERIZIDONE 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 TERIZIDONE. This represents 1.5% of all adverse event reports for TERIZIDONE.
7
Reports of Incorrect product administration duration with TERIZIDONE
1.5%
of all TERIZIDONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From TERIZIDONE?
Of the 7 reports, 3 (42.9%) required hospitalization, and 3 (42.9%) 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 TERIZIDONE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does TERIZIDONE Cause?
Anaemia (74)
Neuropathy peripheral (42)
Electrocardiogram qt prolonged (41)
Drug resistance (39)
Treatment failure (37)
Off label use (28)
Psychotic disorder (27)
Vomiting (27)
Drug-induced liver injury (23)
Renal impairment (23)
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 TERIZIDONE Alternatives Have Lower Incorrect product administration duration Risk?
TERIZIDONE vs TERLIPRESSIN
TERIZIDONE vs TESAMORELIN
TERIZIDONE vs TESTOSTERONE
TERIZIDONE vs TESTOSTERONE CYPIONATE
TERIZIDONE vs TESTOSTERONE ENANTHATE