Does POSACONAZOLE Cause Incorrect product administration duration? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Incorrect product administration duration have been filed in association with POSACONAZOLE (POSACONAZOLE). This represents 0.1% of all adverse event reports for POSACONAZOLE.
6
Reports of Incorrect product administration duration with POSACONAZOLE
0.1%
of all POSACONAZOLE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Incorrect product administration duration From POSACONAZOLE?
Of the 6 reports, 5 (83.3%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POSACONAZOLE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does POSACONAZOLE Cause?
Drug ineffective (785)
Product use in unapproved indication (661)
Off label use (430)
Drug interaction (383)
Death (369)
Condition aggravated (214)
Pyrexia (185)
Neutropenia (181)
Product use issue (181)
Febrile neutropenia (178)
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 POSACONAZOLE Alternatives Have Lower Incorrect product administration duration Risk?
POSACONAZOLE vs POTASSIUM
POSACONAZOLE vs POTASSIUM, DIBASIC
POSACONAZOLE vs POTASSIUM IODIDE
POSACONAZOLE vs POTASSIUM, MONOBASIC
POSACONAZOLE vs POTASSIUM\SODIUM FLUORIDE