Does FLUVASTATIN Cause Intentional product use issue? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Intentional product use issue have been filed in association with FLUVASTATIN (FLUVASTATIN SODIUM ER). This represents 0.8% of all adverse event reports for FLUVASTATIN.
15
Reports of Intentional product use issue with FLUVASTATIN
0.8%
of all FLUVASTATIN reports
15
Deaths
14
Hospitalizations
How Dangerous Is Intentional product use issue From FLUVASTATIN?
Of the 15 reports, 15 (100.0%) resulted in death, 14 (93.3%) required hospitalization, and 14 (93.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUVASTATIN. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does FLUVASTATIN Cause?
Myalgia (577)
Dizziness (304)
Arthralgia (263)
Diarrhoea (260)
Headache (260)
Pruritus (257)
Dyspnoea (234)
Fall (234)
Insomnia (234)
Fatigue (231)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which FLUVASTATIN Alternatives Have Lower Intentional product use issue Risk?
FLUVASTATIN vs FLUVOXAMINE
FLUVASTATIN vs FOLATE
FLUVASTATIN vs FOLIC ACID
FLUVASTATIN vs FOLINIC ACID
FLUVASTATIN vs FOLLICLE STIMULATING HORMONE BETA POLYPEPTIDE\LUTROPIN ALFA