Does ANAGRELIDE Cause Off label use? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Off label use have been filed in association with ANAGRELIDE (Anagrelide). This represents 3.7% of all adverse event reports for ANAGRELIDE.
49
Reports of Off label use with ANAGRELIDE
3.7%
of all ANAGRELIDE reports
3
Deaths
32
Hospitalizations
How Dangerous Is Off label use From ANAGRELIDE?
Of the 49 reports, 3 (6.1%) resulted in death, 32 (65.3%) required hospitalization, and 1 (2.0%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAGRELIDE. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does ANAGRELIDE Cause?
Headache (86)
Anaemia (78)
Palpitations (72)
Platelet count increased (61)
Dyspnoea (60)
Cardiac failure (56)
Cerebral infarction (52)
Fatigue (46)
Drug ineffective (44)
Diarrhoea (41)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which ANAGRELIDE Alternatives Have Lower Off label use Risk?
ANAGRELIDE vs ANAKINRA
ANAGRELIDE vs ANAMORELIN
ANAGRELIDE vs ANASTROZOLE
ANAGRELIDE vs ANDEXANET ALFA
ANAGRELIDE vs ANDROGEL