Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Rosuvastatin
Drug ID BADD_D01971
Description Rosuvastatin, also known as the brand name product Crestor, is a lipid-lowering drug that belongs to the statin class of medications, which are used to lower the risk of cardiovascular disease and manage elevated lipid levels by inhibiting the endogenous production of cholesterol in the liver. More specifically, statin medications competitively inhibit the enzyme hydroxymethylglutaryl-coenzyme A (HMG-CoA) Reductase,[A181421] which catalyzes the conversion of HMG-CoA to mevalonic acid and is the third step in a sequence of metabolic reactions involved in the production of several compounds involved in lipid metabolism and transport including cholesterol, low-density lipoprotein (LDL) (sometimes referred to as "bad cholesterol"), and very low-density lipoprotein (VLDL). Prescribing of statin medications is considered standard practice following any cardiovascular events and for people with a moderate to high risk of development of CVD, such as those with Type 2 Diabetes. The clear evidence of the benefit of statin use coupled with very minimal side effects or long term effects has resulted in this class becoming one of the most widely prescribed medications in North America.[A181087, A181406]
Indications and Usage The FDA monograph states that rosuvastatin is indicated as an adjunct to diet in the treatment of triglyceridemia, Primary Dysbetalipoproteinemia (Type III Hyperlipoproteinemia), and Homozygous Familial Hypercholesterolemia.[F4649] The Health Canada monograph for rosuvastatin further specifies that rosuvastatin is indicated for the reduction of elevated total cholesterol (Total-C), LDL-C, ApoB, the Total-C/HDL-C ratio and triglycerides (TG) and for increasing HDL-C in hyperlipidemic and dyslipidemic conditions when response to diet and exercise alone has been inadequate. It is also indicated for the prevention of major cardiovascular events (including risk of myocardial infarction, nonfatal stroke, and coronary artery revascularization) in adult patients without documented history of cardiovascular or cerebrovascular events, but with at least two conventional risk factors for cardiovascular disease.[F4652] Prescribing of statin medications is considered standard practice following any cardiovascular events and for people with a moderate to high risk of development of CVD. Statin-indicated conditions include diabetes mellitus, clinical atherosclerosis (including myocardial infarction, acute coronary syndromes, stable angina, documented coronary artery disease, stroke, trans ischemic attack (TIA), documented carotid disease, peripheral artery disease, and claudication), abdominal aortic aneurysm, chronic kidney disease, and severely elevated LDL-C levels.[A181087, A181406]
Marketing Status approved
ATC Code C10AA07
DrugBank ID DB01098
KEGG ID D08492
MeSH ID D000068718
PubChem ID 446157
TTD Drug ID D0JE2E
NDC Product Code 70269-400; 16729-286; 31722-882; 31722-884; 50268-710; 47335-985; 68071-2816; 70518-3519; 47335-986; 69238-1149; 71335-1446; 68071-2885; 68788-7971; 31722-883; 47335-984; 47335-987; 50090-2725; 50228-117; 50268-711; 61919-786; 69238-1148; 72189-065; 55700-978; 68071-2848; 68788-7673; 31722-885; 69238-1146; 50228-118; 50268-709; 16729-285; 16729-287; 50090-2724; 71205-044; 71335-0749; 50228-116; 50228-119; 69238-1147; 70771-1483; 71335-0606; 16729-284; 55700-575
UNII 413KH5ZJ73
Synonyms Rosuvastatin Calcium | Calcium, Rosuvastatin | Crestor | Rosuvastatin | ZD4522 | ZD 4522
Chemical Information
Molecular Formula C22H28FN3O6S
CAS Registry Number 287714-41-4
SMILES CC(C)C1=NC(=NC(=C1C=CC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)N(C)S(=O)(=O)C
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Hypophagia19.09.01.004; 14.03.01.006; 07.01.06.0100.000026%Not Available
Lichenoid keratosis23.01.01.0040.000026%Not Available
Skin haemorrhage23.06.07.001; 24.07.01.103--Not Available
Muscle swelling15.05.03.015--Not Available
Chronic kidney disease20.01.03.0170.000051%
Joint instability15.01.08.0070.000017%Not Available
Tendon pain15.07.01.0090.000046%Not Available
Mixed liver injury09.01.07.0150.000017%Not Available
Liver injury09.01.07.022; 12.01.17.0120.000503%Not Available
Organising pneumonia22.01.02.0080.000026%Not Available
Adverse reaction08.06.01.018--Not Available
Type 2 diabetes mellitus14.06.01.003; 05.06.01.003--Not Available
Brain injury17.11.01.003; 19.07.03.007--Not Available
Hypertransaminasaemia09.01.02.0050.000080%Not Available
Oropharyngeal discomfort22.12.03.015; 07.05.05.0080.000017%Not Available
Acute kidney injury20.01.03.0160.000667%
Drug-induced liver injury12.03.01.044; 09.01.07.0230.000837%Not Available
Sinus node dysfunction02.03.03.0170.000017%
Multiple organ dysfunction syndrome08.01.03.0570.000060%
Abnormal loss of weight14.03.02.0190.000017%Not Available
Amyotrophy17.05.03.014; 15.05.05.0100.000043%Not Available
Coeliac disease14.02.01.007; 10.04.04.012; 07.17.01.0080.000058%Not Available
Neuralgic amyotrophy15.05.05.017; 10.04.10.014; 17.09.03.018--Not Available
Overweight14.03.02.0210.000058%Not Available
Post-traumatic stress disorder19.06.06.0020.000058%Not Available
Sleep disorder due to general medical condition, insomnia type19.02.04.0040.000017%Not Available
Intestinal villi atrophy07.11.03.0100.000026%Not Available
Cell death14.11.02.005; 08.03.03.0030.000017%Not Available
Hypertensive cardiomyopathy24.08.05.006; 02.04.01.0090.000026%Not Available
Thalamus haemorrhage24.07.04.033; 17.08.01.0620.000017%Not Available
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