Does BUSULFAN Cause Incorrect product administration duration? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Incorrect product administration duration have been filed in association with BUSULFAN (Busulfan). This represents 0.2% of all adverse event reports for BUSULFAN.
27
Reports of Incorrect product administration duration with BUSULFAN
0.2%
of all BUSULFAN reports
10
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From BUSULFAN?
Of the 27 reports, 10 (37.0%) resulted in death, 2 (7.4%) required hospitalization, and 3 (11.1%) 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 BUSULFAN. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does BUSULFAN Cause?
Off label use (1,402)
Product use in unapproved indication (1,387)
Mucosal inflammation (880)
Venoocclusive liver disease (765)
Febrile neutropenia (628)
Cytomegalovirus infection (620)
Drug ineffective (569)
Graft versus host disease (507)
Pyrexia (502)
Cytomegalovirus infection reactivation (481)
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 BUSULFAN Alternatives Have Lower Incorrect product administration duration Risk?
BUSULFAN vs BUSULFEX
BUSULFAN vs BUTALBITAL
BUSULFAN vs BUTENAFINE
BUSULFAN vs BUTORPHANOL
BUSULFAN vs BUTRANS