Does DELAMANID Cause Incorrect drug administration duration? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Incorrect drug administration duration have been filed in association with DELAMANID. This represents 1.8% of all adverse event reports for DELAMANID.
29
Reports of Incorrect drug administration duration with DELAMANID
1.8%
of all DELAMANID reports
6
Deaths
18
Hospitalizations
How Dangerous Is Incorrect drug administration duration From DELAMANID?
Of the 29 reports, 6 (20.7%) resulted in death, 18 (62.1%) required hospitalization, and 6 (20.7%) were considered life-threatening.
Is Incorrect drug administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DELAMANID. However, 29 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 drug administration duration?
ETONOGESTREL (1,796)
POLYETHYLENE GLYCOL 3350 (1,722)
NAPROXEN (1,272)
DOCOSANOL (803)
ETHINYL ESTRADIOL\ETONOGESTREL (740)
NICOTINE (561)
RANITIDINE (504)
GUAIFENESIN (490)
INSULIN LISPRO (367)
ACETAMINOPHEN (340)
Which DELAMANID Alternatives Have Lower Incorrect drug administration duration Risk?
DELAMANID vs DELANDISTROGENE MOXEPARVOVEC-ROKL
DELAMANID vs DELAVIRDINE
DELAMANID vs DELORAZEPAM
DELAMANID vs DELTA.8-TETRAHYDROCANNABINOL\HERBALS
DELAMANID vs DEMCIZUMAB