سعر كريستاتين 10 مجم 30 قرص مغلف 2024

Crestatin 10 mg 30 f.c. tabs.: rosuvastatin 10 mg film-coated tablets (Adwia).

• Treatment of hypercholesterolaemia and prevention of cardiovascular events (Adwia Crestatin product page — Egyptian manufacturer claim)Population: Adults / adolescents / children ≥6 years per manufacturer textAdwia manufacturer site
• Reduce the risk of major adverse cardiovascular events in adults at increased risk for CV eventsPopulation: AdultsDailyMed (FDA SPL)
• Adjunct to diet and exercise to reduce LDL-C in adults with primary hypercholesterolemiaPopulation: AdultsDailyMed (FDA SPL)

• Most frequent adverse reactions (≥2%): headache, nausea, myalgia, asthenia, constipation.International label, same formulation · DailyMed (FDA SPL)

• Acute liver failure or decompensated cirrhosis.International label, same formulation · DailyMed (FDA SPL)
• Hypersensitivity to rosuvastatin or any excipients (rash, pruritus, urticaria, angioedema reported).International label, same formulation · DailyMed (FDA SPL)

• Myopathy and rhabdomyolysis: risk factors include age ≥65, uncontrolled hypothyroidism, renal impairment, interacting drugs, higher dose, and Asian ancestry. Discontinue if markedly elevated CK or myopathy suspected.International label, same formulation · DailyMed (FDA SPL)
• Hepatic dysfunction: increases in serum transaminases reported; rare fatal/non-fatal hepatic failure. Consider liver enzymes before initiation and as clinically indicated.International label, same formulation · DailyMed (FDA SPL)
• Immune-mediated necrotizing myopathy (IMNM) rarely reported with statins; discontinue if suspected.International label, same formulation · DailyMed (FDA SPL)

• CyclosporineMajorDo not exceed rosuvastatin 5 mg once daily with cyclosporine (exposure increased ~7-fold).DailyMed (FDA SPL)
• GemfibrozilMajorAvoid concomitant use; if unavoidable initiate 5 mg and do not exceed 10 mg once daily.DailyMed (FDA SPL)
• WarfarinModerateObtain INR before starting rosuvastatin; monitor INR frequently until stable after initiation, titration, or discontinuation.DailyMed (FDA SPL)

• Discontinue when pregnancy is recognized, or consider ongoing therapeutic need. May cause fetal harm based on mechanism (decreases cholesterol synthesis). Available observational data have not identified a drug-associated risk of major congenital malformations; data on miscarriage insufficient.International label, same formulation · DailyMed (FDA SPL)
• Present in human milk (limited case reports). Breastfeeding not recommended during treatment because of potential serious adverse reactions in the breastfed infant.International label, same formulation · DailyMed (FDA SPL)

• Rosuvastatin: Competitive inhibition of HMG-CoA reductase reduces hepatic cholesterol synthesis and increases LDL-receptor expression.