Does ACETAMINOPHEN\CHLORPHENIRAMINE\SODIUM ASCORBATE Cause Hyperleukocytosis? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Hyperleukocytosis have been filed in association with ACETAMINOPHEN\CHLORPHENIRAMINE\SODIUM ASCORBATE. This represents 46.2% of all adverse event reports for ACETAMINOPHEN\CHLORPHENIRAMINE\SODIUM ASCORBATE.
6
Reports of Hyperleukocytosis with ACETAMINOPHEN\CHLORPHENIRAMINE\SODIUM ASCORBATE
46.2%
of all ACETAMINOPHEN\CHLORPHENIRAMINE\SODIUM ASCORBATE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Hyperleukocytosis From ACETAMINOPHEN\CHLORPHENIRAMINE\SODIUM ASCORBATE?
Of the 6 reports, 6 (100.0%) required hospitalization, and 1 (16.7%) were considered life-threatening.
Is Hyperleukocytosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACETAMINOPHEN\CHLORPHENIRAMINE\SODIUM ASCORBATE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does ACETAMINOPHEN\CHLORPHENIRAMINE\SODIUM ASCORBATE Cause?
Drug abuse (8)
Coma (7)
Psychomotor hyperactivity (7)
Abdominal pain (6)
Acute kidney injury (6)
Electrocardiogram t wave peaked (6)
Heart rate increased (6)
Hyperkalaemia (6)
Hypotension (6)
Intentional overdose (6)
What Other Drugs Cause Hyperleukocytosis?
CYCLOPHOSPHAMIDE (55)
PREDNISONE (54)
TRETINOIN (52)
ARSENIC TRIOXIDE (49)
RITUXIMAB (49)
ACETAMINOPHEN (44)
VINCRISTINE (44)
DEXAMETHASONE (42)
PANTOPRAZOLE (38)
AMOXICILLIN (36)