Does IBRUTINIB Cause Withdrawal syndrome? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Withdrawal syndrome have been filed in association with IBRUTINIB (Imbruvica). This represents 0.0% of all adverse event reports for IBRUTINIB.
29
Reports of Withdrawal syndrome with IBRUTINIB
0.0%
of all IBRUTINIB reports
1
Deaths
8
Hospitalizations
How Dangerous Is Withdrawal syndrome From IBRUTINIB?
Of the 29 reports, 1 (3.4%) resulted in death, 8 (27.6%) required hospitalization, and 1 (3.4%) were considered life-threatening.
Is Withdrawal syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBRUTINIB. However, 29 reports have been filed with the FAERS database.
What Other Side Effects Does IBRUTINIB Cause?
Death (8,007)
Off label use (5,446)
Fatigue (4,479)
Diarrhoea (3,903)
Atrial fibrillation (3,671)
Pneumonia (3,015)
Incorrect dose administered (2,752)
Contusion (2,712)
Fall (2,375)
Asthenia (2,200)
What Other Drugs Cause Withdrawal syndrome?
ACETAMINOPHEN\OXYCODONE (4,046)
PREGABALIN (3,329)
OXYCODONE (2,798)
ACETAMINOPHEN\HYDROCODONE (2,636)
FENTANYL (1,948)
MORPHINE (1,674)
TRAMADOL (1,582)
VENLAFAXINE (1,516)
DULOXETINE (1,328)
BUPRENORPHINE (1,266)
Which IBRUTINIB Alternatives Have Lower Withdrawal syndrome Risk?
IBRUTINIB vs IBUPROFEN
IBRUTINIB vs IBUPROFEN LYSINE
IBRUTINIB vs IBUPROFEN UNKNOWN PRODUCT
IBRUTINIB vs IBUPROFEN\IBUPROFEN
IBRUTINIB vs IBUPROFEN\PHENYLEPHRINE