Does PRAVASTATIN Cause Intentional dose omission? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intentional dose omission have been filed in association with PRAVASTATIN (Pravastatin Sodium). This represents 0.1% of all adverse event reports for PRAVASTATIN.
7
Reports of Intentional dose omission with PRAVASTATIN
0.1%
of all PRAVASTATIN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Intentional dose omission From PRAVASTATIN?
Of the 7 reports, 3 (42.9%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAVASTATIN. However, 7 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 dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which PRAVASTATIN Alternatives Have Lower Intentional dose omission Risk?
PRAVASTATIN vs PRAVASTATIN\PRAVASTATIN
PRAVASTATIN vs PRAZAXA
PRAVASTATIN vs PRAZEPAM
PRAVASTATIN vs PRAZIQUANTEL
PRAVASTATIN vs PRAZOSIN