Does ETHIONAMIDE 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 ETHIONAMIDE. This represents 1.1% of all adverse event reports for ETHIONAMIDE.
7
Reports of Incorrect product administration duration with ETHIONAMIDE
1.1%
of all ETHIONAMIDE reports
2
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From ETHIONAMIDE?
Of the 7 reports, 2 (28.6%) resulted in death, 2 (28.6%) 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 ETHIONAMIDE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does ETHIONAMIDE Cause?
Drug resistance (107)
Vomiting (91)
Anaemia (82)
Nausea (80)
Off label use (68)
Electrocardiogram qt prolonged (65)
Neuropathy peripheral (52)
Tuberculosis (49)
Treatment failure (45)
Diarrhoea (38)
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 ETHIONAMIDE Alternatives Have Lower Incorrect product administration duration Risk?
ETHIONAMIDE vs ETHOSUXIMIDE
ETHIONAMIDE vs ETHYL ICOSAPENTATE
ETHIONAMIDE vs ETHYL LOFLAZEPATE
ETHIONAMIDE vs ETHYLENE GLYCOL
ETHIONAMIDE vs ETIFOXINE