Does CRESTOR Cause Intentional product misuse? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Intentional product misuse have been filed in association with CRESTOR. This represents 4.0% of all adverse event reports for CRESTOR.
49
Reports of Intentional product misuse with CRESTOR
4.0%
of all CRESTOR reports
2
Deaths
13
Hospitalizations
How Dangerous Is Intentional product misuse From CRESTOR?
Of the 49 reports, 2 (4.1%) resulted in death, 13 (26.5%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CRESTOR. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does CRESTOR Cause?
Type 2 diabetes mellitus (342)
Cardiovascular disorder (319)
Myocardial infarction (135)
Myalgia (87)
Drug dose omission (83)
Blood cholesterol increased (75)
Off label use (60)
Drug hypersensitivity (51)
Drug ineffective (48)
Malaise (48)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which CRESTOR Alternatives Have Lower Intentional product misuse Risk?
CRESTOR vs CRISABOROLE
CRESTOR vs CRIZANLIZUMAB
CRESTOR vs CRIZANLIZUMAB-TMCA
CRESTOR vs CRIZOTINIB
CRESTOR vs CROFELEMER