Does DELAMANID Cause Incorrect product administration duration? 80 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 80 reports of Incorrect product administration duration have been filed in association with DELAMANID. This represents 4.9% of all adverse event reports for DELAMANID.
80
Reports of Incorrect product administration duration with DELAMANID
4.9%
of all DELAMANID reports
27
Deaths
33
Hospitalizations
How Dangerous Is Incorrect product administration duration From DELAMANID?
Of the 80 reports, 27 (33.8%) resulted in death, 33 (41.3%) required hospitalization, and 5 (6.3%) 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 DELAMANID. However, 80 reports have been filed with the FAERS database.
What Other Side Effects Does DELAMANID Cause?
Electrocardiogram qt prolonged (263)
Vomiting (237)
Anaemia (209)
Off label use (207)
Dyspnoea (160)
Neuropathy peripheral (135)
Nausea (126)
Haemoglobin decreased (104)
Tuberculosis (94)
Intentional product use issue (89)
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 DELAMANID Alternatives Have Lower Incorrect product administration duration Risk?
DELAMANID vs DELANDISTROGENE MOXEPARVOVEC-ROKL
DELAMANID vs DELAVIRDINE
DELAMANID vs DELORAZEPAM
DELAMANID vs DELTA.8-TETRAHYDROCANNABINOL\HERBALS
DELAMANID vs DEMCIZUMAB