What is Statix?
Statix is in a group of drugs called HMG CoA reductase inhibitors, or "statins." Statix reduces levels of "bad" cholesterol (low-density lipoprotein, or LDL) and triglycerides in the blood, while increasing levels of "good" cholesterol (high-density lipoprotein, or HDL).
Statix is used to treat high cholesterol, and to lower the risk of stroke, heart attack, or other heart complications in people with type 2 diabetes, coronary heart disease, or other risk factors.
Statix is used in adults and children who are at least 10 years old.
Statix may also be used for purposes not listed in this medication guide.
Statix indications
Statix is indicated as an adjunct to diet for the treatment of patients with elevated total cholesterol (total-C), low density lipoprotein cholesterol (LDL-C), apolipoprotein B (apo B), and triglycerides (TG) and to increase high density lipoprotein cholesterol (HDL-C) in patients with primary hypercholesterolemia (heterozygous familial and non-familial hypercholesterolemia), combined (mixed) hyperlipidemia (Fredrickson Types IIa and IIb), elevated serum TGlevels (Fredrickson Type IV), and for patients with dysbetalipoproteinemia (Fredrickson Type III) who do not respond adequately to diet.
Statix is also indicated for the reduction of total-C and LDL-C in patients with homozygous familial hypercholesterolemia.
Prevention of Cardiovascular Complications: In patients without clinically evident cardiovascular disease (CVD), and with or without dyslipidemia, but with multiple risk factors for coronary heart disease (CHD), such as smoking, hypertension, diabetes, low HDL-C, or a family history of early CHD, Statix is indicated to: Reduce the risk of fatal CHD and non-fatal myocardial infarction (MI); reduce the risk of stroke; reduce the risk of revascularization procedures and angina pectoris.
In patients with clinically evident CHD, Statix is indicated to: Reduce the risk of non-fatal MI; reduce the risk of fatal and non-fatal stroke; reduce the risk for revascularization procedures; reduce the risk of hospitalization for congestive heart failure (CHF); reduce the risk of angina.
As adjunct to lifestyle changes, such as proper diet and exercise, intensive Statix treatment has been shown to halt the progression of atherosclerosis (total atheroma or plaque volume) in patients with coronary artery disease and other individuals who are at high risk for cardiovascular disease.
Chronic Kidney Disease: In patients with diabetes with moderately decreased eGFR, Statix is indicated to reduce the risk for cardiovascular disease.
In patients with clinically evident coronary heart disease and CKD not requiring dialysis, Statix is indicated to reduce the risk of major cardiovascular events including stroke.
In patients with clinically evident coronary heart disease and/or diabetes with microalbuminuria, Statix is indicated to reduce the rate of GFR decline and progression of CKD.
Pediatric Patients (10-17 Years of Age): Statix is indicated as an adjunct to diet to reduce total-C, LDL-C, and apo B levels in boys and post-menarchal girls, 10 to 17 years of age, with heterozygous familial hyperchlolesterolemia if, after an adequate trial of diet therapy, the following findings are present: LDL-C remains ≥190 mg/dL or, LDL-C remains ≥160 mg/dL and there is a positive family history of premature CVD or, two or more other CVD risk factors are present in the pediatric patient.
How should I use Statix?
Use Statix as directed by your doctor. Check the label on the medicine for exact dosing instructions.
- An extra patient leaflet is available with Statix. Talk to your pharmacist if you have questions about this information.
- Take Statix by mouth with or without food.
- Swallow Statix whole. Do not break, crush, or chew before swallowing.
- Taking Statix at the same time each day will help you remember to take it.
- Eating grapefruit or drinking grapefruit juice may increase the amount of Statix in your blood, which may increase your risk for serious side effects. The risk may be greater with large amounts of grapefruit or grapefruit juice. Avoid large amounts of grapefruit or grapefruit juice (eg, more than 1 quart daily). Talk with your doctor or pharmacist if you have questions about including grapefruit or grapefruit juice in your diet while you are taking Statix.
- Continue to take Statix even if you feel well. Do not miss any doses.
- If you miss a dose of Statix, take it as soon as possible if you remember within 12 hours of the missed dose. If it is more than 12 hours since the missed dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.
Ask your health care provider any questions you may have about how to use Statix.
Uses of Statix in details
Use: Labeled Indications
Heterozygous familial hypercholesterolemia: To reduce elevated total cholesterol (total-C), LDL cholesterol (LDL-C), apolipoprotein B (apo B), and triglyceride levels, and to increase HDL cholesterol in patients with primary hypercholesterolemia.
Heterozygous familial hypercholesterolemia (pediatrics): To reduce total-C, LDL-C, and apo B levels in pediatric patients 10 to 17 years of age with heterozygous familial hypercholesterolemia with LDL-C ≥190 mg/dL, LDL-C ≥160 mg/dL with positive family history of premature cardiovascular disease (CVD), or LDL-C ≥160 mg/dL with 2 or more other CVD risk factors.
Homozygous familial hypercholesterolemia: To reduce total-C and LDL-C in patients with homozygous familial hypercholesterolemia as an adjunct to other lipid-lowering treatments (eg, LDL apheresis) or if such treatments are unavailable.
Prevention of atherosclerotic cardiovascular disease:
Primary prevention of atherosclerotic cardiovascular disease (ASCVD): To reduce the risk of myocardial infarction (MI), stroke, revascularization procedures, and angina in adult patients without a history of coronary heart disease (CHD) but who have multiple CHD risk factors.
Secondary prevention in patients with established ASCVD: To reduce the risk of MI, stroke, revascularization procedures, and angina in patients with a history of CHD.
Off Label Uses
Transplantation, post heart or post kidney
Based on the 2010 International Society of Heart and Lung Transplantation guidelines for the care of heart transplant recipients, Statix is effective and recommended following heart transplant, regardless of cholesterol levels, to reduce cardiac allograft vasculopathy and improve long-term outcomes.
Based on the 2013 Kidney Disease: Improving Global Outcomes clinical practice guideline for lipid management in chronic kidney disease, Statix is suggested following kidney transplant to reduce cardiovascular events (eg, myocardial infarction, stroke, cardiovascular death).
Statix description
Statix 10: Each tablet contains Atorvastatin calcium equivalent to 10 mg Statix.
Statix 20 mg: Each tablet contains Atorvastatin calcium equivalent to 20 mg Statix.
Statix 40 mg: Each tablet contains Atorvastatin calcium equivalent to 40 mg Statix.
Statix 80 mg: Each tablet contains atorvastin calcium equivalent to 80 mg Statix.
Statix is a white, elliptical film coated tablet containing Statix calcium. Statix calcium is a synthetic lipid-lowering agent, which is an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase. This enzyme catalyzes the conversion of HMG-CoA to mevalonate, an early and rate-limiting step in cholesterol biosynthesis.
The empirical formula of Statix calcium is (C33H34FN2O5)2Ca·3H2O and its molecular weight is 1209.42.
Statix calcium is a white to off-white crystalline powder, practically insoluble in aqueous solutions of pH 4 and below. It is very slightly soluble in distilled water, pH 7.4 phosphate buffer, and acetonitrile; slightly soluble in ethanol; and freely soluble in methanol.
Statix dosage
Always take Statix Sandoz exactly as prescribed.
The following instructions may apply only if the doctor has not prescribed a different regimen for administering Statix Sandoz. Observe the instructions closely, otherwise the medicine cannot be effective.
Before the start of treatment, the physician will prescribe a low-cholesterol diet and should be strictly observe throughout the treatment with Statix Sandoz.
Usual Starting Dose: Adults and Children ≥10 years: 10 mg once daily. The physician will determine further doses to achieve the desired blood cholesterol levels. Thereafter, the dose will be adjusted individually every ≤4 weeks frequently. Maximum Daily Dose: 80 mg for adults and 20 mg once daily for children.
Elevated Blood Cholesterol Levels (Hypercholesterolemia) or Concurrent Elevation of Blood Cholesterol and Triglyceride Levels (Mixed Hyperlipidemia): In the majority of patients, the effective daily dose of Statix is 20 mg. The effect of treatment can be seen after 2 weeks; it is usually greatest after 4 weeks. This therapeutic effect is then maintained with long-term administration of Statix Sandoz.
Hereditary Increase of Blood Cholesterol Levels (Familial Hypercholesterolemia): Heterozygous Familial Hypercholesterolemia: Starting Dose: 10 mg once daily. The dose should be determined for each individual patient. The physician will increases the dose up to 80 mg daily every 4 weeks.
Homozygous Familial Hypercholesterolemia: Adults: In the majority of patients (taking Statix 80 mg daily), blood cholesterol levels (LDL cholesterol) decreased by 17-31% in clinical trials.
Patients with Renal Insufficiency and the Elderly:
In clinical trials, it was ascertained that no dosage adjustment is necessary in elderly patients.
Administration: Take Statix Sandoz with some liquid at any time of the day and regardless of food intake.
Statix Sandoz are designated for long-term administration.
Missed Dose: Do not take a double dose, but only the normal dose.
Statix interactions
See also:
What other drugs will affect Statix?
The risk of myopathy during treatment with statins is increased with concurrent administration of fibric acid derivatives, lipid-modifying doses of niacin, cyclosporine, or strong CYP 3A4 inhibitors (e.g., clarithromycin, HIV protease inhibitors, and itraconazole).
Strong Inhibitors of CYP 3A4
Statix is metabolized by cytochrome P450 3A4. Concomitant administration of Statix with strong inhibitors of CYP 3A4 can lead to increases in plasma concentrations of Statix. The extent of interaction and potentiation of effects depend on the variability of effect on CYP 3A4.
Clarithromycin
Statix AUC was significantly increased with concomitant administration of Statix 80 mg with clarithromycin (500 mg twice daily) compared to that of Statix alone. Therefore, in patients taking clarithromycin, caution should be used when the Statix dose exceeds 20 mg.
Combination of Protease Inhibitors
Statix AUC was significantly increased with concomitant administration of Statix 40 mg with ritonavir plus saquinavir (400 mg twice daily) or Statix 20 mg with lopinavir plus ritonavir (400 mg + 100 mg twice daily) compared to that of Statix alone. Therefore, in patients taking HIV protease inhibitors, caution should be used when the Statix dose exceeds 20 mg.
Itraconazole
Statix AUC was significantly increased with concomitant administration of Statix 40 mg and itraconazole 200 mg. Therefore, in patients taking itraconazole, caution should be used when the Statix dose exceeds 20 mg.
Grapefruit Juice
Contains one or more components that inhibit CYP 3A4 and can increase plasma concentrations of Statix, especially with excessive grapefruit juice consumption ( > 1.2 liters per day).
Cyclosporine
Statix and Statix-metabolites are substrates of the OATP1B1 transporter. Inhibitors of the OATP1B1 (e.g., cyclosporine) can increase the bioavailability of Statix. Statix AUC was significantly increased with concomitant administration of Statix 10 mg and cyclosporine 5.2 mg/kg/day compared to that of Statix alone. In cases where co-administration of Statix with cyclosporine is necessary, the dose of Statix should not exceed 10 mg.
Rifampin or other Inducers of Cytochrome P450 3A4
Concomitant administration of Statix with inducers of cytochrome P450 3A4 (e.g., efavirenz, rifampin) can lead to variable reductions in plasma concentrations of Statix. Due to the dual interaction mechanism of rifampin, simultaneous co-administration of Statix with rifampin is recommended, as delayed administration of Statix after administration of rifampin has been associated with a significant reduction in Statix plasma concentrations.
Digoxin
When multiple doses of Statix and digoxin were coadministered, steady state plasma digoxin concentrations increased by approximately 20%. Patients taking digoxin should be monitored appropriately.
Oral Contraceptives
Co-administration of Statix and an oral contraceptive increased AUC values for norethindrone and ethinyl estradiol. These increases should be considered when selecting an oral contraceptive for a woman taking Statix.
Warfarin
Statix had no clinically significant effect on prothrombin time when administered to patients receiving chronic warfarin treatment.
Statix side effects
See also:
What are the possible side effects of Statix?
Adverse reactions have usually been mild and transient. Less than 2% of patients were discontinued from clinical trials due to adverse reactions attributed to Statix.
The most frequent (≥1%) adverse effects associated with Statix therapy, in patients participating in controlled clinical studies were: Psychiatric Disorders: Insomnia.
Nervous System Disorders: Headache.
Gastrointestinal Disorders: Abdominal pain, dyspepsia, nausea, flatulence, constipation, diarrhea.
Musculoskeletal and Connective Tissue Disorders: Myalgia.
General Disorders and Administration Site Conditions: Asthenia.
Elevated serum ALT levels have been reported in 1.3% of patients receiving Statix. Clinically important (>3 x UNL) elevations in serum ALT levels occurred in 19 of the 2,483 (0.8%) patients on Statix. It was dose-related and was reversible in all 19 patients. In 10 cases, the increase was first observed within 12 weeks of starting the treatment. Only 1 case occurred after 36 weeks and only 1 patient had symptoms suggestive of hepatitis. Treatment was discontinued in only 9 of these 19 cases.
Elevated serum CPK levels (>3x ULN) occurred in 62 of the 2,452 (2.5%) patients on Statix compared with 3.1% with other HMG-CoA reductase inhibitors in clinical trials. Levels >10 times the normal upper range occurred in only 11 (0.4%) Statix-treated patients. Only 3 (0.1%) of these 11 patients had concurrent muscle pain, tenderness or weakness.
Statix contraindications
See also:
What is the most important information I should know about Statix?
Active liver disease, which may include unexplained persistent elevations in hepatic transaminase levels
Hypersensitivity to any component of this medication
Pregnancy
Women who are pregnant or may become pregnant. Statix may cause fetal harm when administered to a pregnant woman. Serum cholesterol and triglycerides increase during normal pregnancy, and cholesterol or cholesterol derivatives are essential for fetal development. Atherosclerosis is a chronic process and discontinuation of lipid-lowering drugs during pregnancy should have little impact on the outcome of long-term therapy of primary hypercholesterolemia. There are no adequate and well-controlled studies of Statix use during pregnancy; however in rare reports, congenital anomalies were observed following intrauterine exposure to statins. In rat and rabbit animal reproduction studies, Statix revealed no evidence of teratogenicity. Statix SHOULD BE ADMINISTERED TO WOMEN OF CHILDBEARING AGE ONLY WHEN SUCH PATIENTS ARE HIGHLY UNLIKELY TO CONCEIVE AND HAVE BEEN INFORMED OF THE POTENTIAL HAZARDS. If the patient becomes pregnant while taking this drug, Statix should be discontinued immediately and the patient apprised of the potential hazard to the fetus.
Nursing mothers
It is not known whether Statix is excreted into human milk; however a small amount of another drug in this class does pass into breast milk. Because statins have the potential for serious adverse reactions in nursing infants, women who require Statix treatment should not breastfeed their infants.
Active ingredient matches for Statix:
Atorvastatin in India.
| Unit description / dosage (Manufacturer) | Price, USD |
| Statix 10mg TAB / 10 | $ 0.83 |
| Statix 20mg TAB / 10 | $ 1.55 |
| Statix 40mg TAB / 10 | $ 2.23 |
| 10 mg x 10's | $ 0.83 |
| 20 mg x 10's | $ 1.55 |
| 40 mg x 10's | $ 2.23 |
| 80 mg | |
| Statix 40 mg Tablet | $ 0.23 |
| Statix 20 mg Tablet | $ 0.17 |
| Statix 10 mg Tablet | $ 0.09 |
| Statix 80 mg Tablet | $ 0.31 |
| Statix 10mg FC-TAB / 10 | $ 0.83 |
| Statix 20mg FC-TAB / 10 | $ 1.55 |
| Statix 40mg FC-TAB / 10 | $ 2.23 |
| Statix 80mg FC-TAB | |
| STATIX 10MG TABLET 1 strip / 10 tablets each (Biocon) | $ 0.64 |
| STATIX 20 MG TABLET 1 strip / 10 tablets each (Biocon) | $ 1.52 |
| STATIX 40MG TABLET 1 strip / 10 tablets each (Biocon) | $ 2.27 |
| STATIX 80MG TABLET 1 strip / 10 tablets each (Biocon) | $ 3.64 |
| STATIX film-coated tab 10 mg x 10's (Biocon) | $ 1.00 |
| STATIX film-coated tab 20 mg x 10's (Biocon) | $ 1.86 |
| STATIX film-coated tab 40 mg x 10's (Biocon) | $ 2.35 |
| STATIX film-coated tab 80 mg x 10's (Biocon) | $ 3.31 |
| Statix 10mg Tablet (Biocon) | $ 0.07 |
| Statix 20mg Tablet (Biocon) | $ 0.15 |
| Statix 40mg Tablet (Biocon) | $ 0.23 |
| Statix 80mg Tablet (Biocon) | $ 0.36 |
List of Statix substitutes (brand and generic names): | |
| Statinor (Tunisia) | |
| STATLIP | |
| STATLIP Capsule/ Tablet / 20mg / 10 units (Wander Ltd) | $ 1.33 |
| STATLIP Capsule/ Tablet / 10mg / 10 units (Wander Ltd) | $ 0.72 |
| Statlip 5 mg Tablet (Wander Ltd) | $ 0.07 |
| Statlip 10 mg Tablet (Wander Ltd) | $ 0.07 |
| Statlip 20 mg Tablet (Wander Ltd) | $ 0.13 |
| STATLIP 10MG TABLET 1 strip / 10 tablets each (Wander Ltd) | $ 0.72 |
| STATLIP 20MG TABLET 1 strip / 10 tablets each (Wander Ltd) | $ 1.33 |
| Statlip 10mg Tablet (Wander Ltd) | $ 0.07 |
| Statlip 20mg Tablet (Wander Ltd) | $ 0.13 |
| Statol (Cyprus) | |
| Stator -AM | |
| Stator -AM Atorvastatin 10mg, Amlodipine5mg TAB / 10 | $ 0.58 |
| Stator AM | |
| Stator AM 10+5 Tablet (Piramal Healthcare) | $ 0.06 |
| Stator F | |
| Stator F 10+160 Tablet (Piramal Healthcare) | $ 0.08 |
| STATOR F TABLET 1 strip / 10 tablets each (Piramal Healthcare) | $ 1.23 |
| Stator R | |
| Stator R 10+2.5 Tablet (Piramal Healthcare) | $ 0.05 |
| Stator R 10+5 mg Tablet (Piramal Healthcare) | $ 0.07 |
| Stator-GM1 (India) | |
| Stator-GM1 Metformin / SR 500 mg, Glimepiride 1 mg, Atorvastatin10 mg. Bilayered TAB / 10 (AHPL) | $ 0.93 |
| 10's (AHPL) | $ 0.93 |
| STATOR-GM1 bilayer coated tab 10's (AHPL) | $ 0.93 |
| Stator-GM2 (India) | |
| Stator-GM2 Metformin / SR 500 mg, Glimepiride 2 mg, Atorvastatin10 mg. Bilayered TAB / 10 (AHPL) | $ 1.01 |
| 10's (AHPL) | $ 1.01 |
| STATOR-GM2 bilayer coated tab 10's (AHPL) | $ 1.01 |
| Statorva (Poland) | |
| Statrox (India) | |
| Statrox 10mg TAB / 10 (Wonder (Asrox)) | $ 0.72 |
| STATROX tab 10 mg x 10's (Wonder (Asrox)) | $ 0.72 |
| Statwa | |
| Statwa 20 mg Tablet (Kaytross Healthcare Limited) | $ 0.15 |
| Statwa 5 mg Tablet (Kaytross Healthcare Limited) | $ 0.06 |
| Statwa 10 mg Tablet (Kaytross Healthcare Limited) | $ 0.10 |
| Stavinor (Indonesia) | |
| Stavra (Georgia) | |
| Storclop | |
| Storclop 10+75 Capsule (Ranbaxy Laboratories Ltd.,) | $ 0.13 |
| Stortin | |
| Stortin 10 mg Tablet (Perk Pharmaceuticals Ltd.) | $ 0.05 |
| Storvas (Bulgaria, India, Myanmar, Oman, Peru, Vietnam) | |
| STORVAS Capsule/ Tablet / 20mg / 10 units (Cardiovascular (Ranbaxy Laboratories Ltd)) | $ 2.17 |
| STORVAS Capsule/ Tablet / 10mg / 10 units (Cardiovascular (Ranbaxy Laboratories Ltd)) | $ 1.12 |
| STORVAS Capsule/ Tablet / 5mg / 10 units (Cardiovascular (Ranbaxy Laboratories Ltd)) | $ 0.69 |
| Storvas 10mg FC-TAB / 10 (Cardiovascular (Ranbaxy Laboratories Ltd)) | $ 1.12 |
| Storvas 20mg FC-TAB / 10 (Cardiovascular (Ranbaxy Laboratories Ltd)) | $ 2.17 |
| Storvas 10 mg x 1 Blister x 10 Tablet (Cardiovascular (Ranbaxy Laboratories Ltd)) | |
| Storvas 10 mg x 3 Blister x 10 Tablet (Cardiovascular (Ranbaxy Laboratories Ltd)) | |
| Storvas 10 mg x 10 Blister x 10 Tablet (Cardiovascular (Ranbaxy Laboratories Ltd)) | |
| Storvas 20 mg x 1 Blister x 10 Tablet (Cardiovascular (Ranbaxy Laboratories Ltd)) | |
See 4287 substitutes for Statix | |
References
- DailyMed. "AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
- PubChem. "atorvastatin". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
- DrugBank. "atorvastatin". http://www.drugbank.ca/drugs/DB01076 (accessed September 17, 2018).
Reviews
The results of a survey conducted on ndrugs.com for Statix are given in detail below. The results of the survey conducted are based on the impressions and views of the website users and consumers taking Statix. We implore you to kindly base your medical condition or therapeutic choices on the result or test conducted by a physician or licensed medical practitioners.User reports
Consumer reported useful
No survey data has been collected yetConsumer reported price estimates
No survey data has been collected yetConsumer reported time for results
No survey data has been collected yet1 consumer reported age
| Users | % | ||
|---|---|---|---|
| 46-60 | 1 | 100.0% | |
Consumer reviews
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Information checked by Dr. Sachin Kumar, MD Pharmacology
