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TOVAST 10/MG FC TAB 30/FC TAB
TOVAST 10/MG FC TAB 30/FC TAB
43.45
TOVAST 10/MG FC TAB 30/FC TAB
Frequently bought together
Brand : TOVAST

TOVAST 10/MG FC TAB 30/FC TAB

43.45
  • Sku : I-006324
  • Key features

    TOVAST 10 mg film-coated tablets contain the active ingredient atorvastatin calcium. It works by selectively and competitively inhibiting HMG-CoA reductase, reducing hepatic cholesterol synthesis and upregulating LDL receptors to increase LDL clearance. TOVAST is indicated for lowering elevated LDL cholesterol and managing hypercholesterolemia and dyslipidemia. Available by prescription as film-coated tablets in a pack of 30.

     

    • Brand: TOVAST
    • Active Ingredient: ATORVASTATIN CALCIUM
    • Strength: 10mg
    • Dosage Form: Film-coated tablet
    • Pack Size: 30 Tablets
    • Route: Oral use
    • Prescription Status: Prescription
    • Therapeutic Class: Lipid Modifying
    • Pharmacological Group: Statins
    • Manufacturer: SPIMACO
    • Country of Origin: Saudi Arabia
    • SFDA Registration No.: 1411211317
    • Shelf Life: 48 months
    • Storage: do not store above 30°c
    • Lipid Target: Both: Triglycerides & LDL
Frequently bought together
Description
Specification

Indications

Off-Label Uses

No specific off-label uses should be asserted for this product; atorvastatin has been studied off-label in conditions such as NAFLD/NASH and contrast-associated AKI prevention, but these are not established indications.

Dosage & Administration

Initial Dose

10-20mg once daily. [6, 18, 20]

Dose Adjustment Notes

Titrate based on LDL-C response at intervals of about 2-4 weeks; no renal dose adjustment; avoid in active liver disease and use caution/monitor in hepatic impairment; with strong CYP3A4 inhibitors or cyclosporine, avoid or use the lowest necessary dose with close monitoring (some labels recommend not exceeding 10 mg/day with cyclosporine).

Side Effects

Common Side Effects

Nasopharyngitis, arthralgia, diarrhea, pain in extremity, urinary tract infection, dyspepsia, nausea, insomnia, muscle spasms. [1, 6, 22]

Safety & Warnings

Warnings & Precautions

Muscle toxicity: counsel to report unexplained muscle pain/weakness; check CK when clinically indicated and stop if myopathy/rhabdomyolysis suspected; risk increases with interacting drugs (CYP3A4 inhibitors, cyclosporine), high dose, older age, hypothyroidism, renal impairment, and fibrates/niacin/colchicine. Hepatic effects: obtain baseline LFTs and repeat if symptoms/signs of hepatotoxicity occur; avoid in active liver disease and use caution with heavy alcohol use/history of liver disease. Metabolic: may increase glucose/HbA1c-monitor in patients at risk for diabetes.

Age Restriction

Not approved for children under 10 years of age.

Driving Warning

Safe

Drug Interactions

Drug Interactions

Major interactions: strong CYP3A4 inhibitors (e.g., clarithromycin/erythromycin, azole antifungals, HIV protease inhibitors/cobicistat, nefazodone) and grapefruit juice (large amounts) ↑ atorvastatin exposure; cyclosporine ↑ exposure (avoid or use very low dose with close monitoring); hepatitis C antivirals (e.g., glecaprevir/pibrentasvir-contraindicated; some others require limits); fibrates (especially gemfibrozil) and niacin (lipid-lowering doses) ↑ myopathy/rhabdomyolysis risk; colchicine ↑ myopathy risk; warfarin-monitor INR when starting/stopping; digoxin-may ↑ digoxin levels; antacids may slightly ↓ atorvastatin levels (usually not clinically significant).

Food Interaction

May be taken with or without food; avoid large quantities of grapefruit juice (clinically, avoid excessive intake-commonly cited as >1 quart/≈1 liter daily).

Special Populations

Elderly

Standard adult dosing; elderly patients (≥65 years) may be at higher risk for myopathy - monitor closely and use lowest effective dose

Storage & Patient Advice

Stopping the Medicine

Do not stop atorvastatin without consulting the prescriber; if discontinued, LDL-C will rise again and cardiovascular risk reduction is lost.

Pharmacology

Mechanism of Action

Selective, competitive inhibition of HMG-CoA reductase, decreasing hepatic cholesterol synthesis and upregulating LDL receptors to increase LDL clearance.

Duration of Effect

Per dose: ~24 hours (supports once-daily dosing). Lipid-lowering effect: begins within ~2 weeks and reaches near-maximal effect by ~4 weeks with continuous daily therapy.

Product Information

Available Dosage Forms

Film-coated tablet (oral).

OTC Alternatives

No OTC alternative

Lipid Target

Both

 

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The product information provided is derived from verified pharmaceutical references and is intended for general health education only. It is not a substitute for professional medical advice, diagnosis, or treatment.

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  • Any therapeutic decision made based on the information displayed without consulting a licensed physician or pharmacist
  • Any discrepancy between the information provided and the product's package insert or SFDA guidelines
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