Does SIMVASTATIN Cause Wrong patient received product? 48 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Wrong patient received product have been filed in association with SIMVASTATIN (Simvastatin). This represents 0.2% of all adverse event reports for SIMVASTATIN.
48
Reports of Wrong patient received product with SIMVASTATIN
0.2%
of all SIMVASTATIN reports
10
Deaths
22
Hospitalizations
How Dangerous Is Wrong patient received product From SIMVASTATIN?
Of the 48 reports, 10 (20.8%) resulted in death, 22 (45.8%) required hospitalization.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIMVASTATIN. However, 48 reports have been filed with the FAERS database.
What Other Side Effects Does SIMVASTATIN Cause?
Myalgia (3,919)
Fatigue (2,066)
Arthralgia (1,775)
Drug interaction (1,744)
Nausea (1,676)
Rhabdomyolysis (1,616)
Dyspnoea (1,542)
Headache (1,470)
Drug hypersensitivity (1,433)
Muscular weakness (1,356)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which SIMVASTATIN Alternatives Have Lower Wrong patient received product Risk?
SIMVASTATIN vs SINGULAIR
SIMVASTATIN vs SINTILIMAB
SIMVASTATIN vs SIPONIMOD
SIMVASTATIN vs SIPULEUCEL-T
SIMVASTATIN vs SIROLIMUS