Does PRAVASTATIN Cause Intentional product misuse? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Intentional product misuse have been filed in association with PRAVASTATIN (Pravastatin Sodium). This represents 0.3% of all adverse event reports for PRAVASTATIN.
28
Reports of Intentional product misuse with PRAVASTATIN
0.3%
of all PRAVASTATIN reports
17
Deaths
19
Hospitalizations
How Dangerous Is Intentional product misuse From PRAVASTATIN?
Of the 28 reports, 17 (60.7%) resulted in death, 19 (67.9%) required hospitalization, and 19 (67.9%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAVASTATIN. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does PRAVASTATIN Cause?
Myalgia (1,290)
Arthralgia (570)
Dyspnoea (514)
Fatigue (500)
Drug hypersensitivity (493)
Diarrhoea (478)
Headache (448)
Pruritus (432)
Nausea (420)
Dizziness (413)
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 PRAVASTATIN Alternatives Have Lower Intentional product misuse Risk?
PRAVASTATIN vs PRAVASTATIN\PRAVASTATIN
PRAVASTATIN vs PRAZAXA
PRAVASTATIN vs PRAZEPAM
PRAVASTATIN vs PRAZIQUANTEL
PRAVASTATIN vs PRAZOSIN