Santinal MR
Dipyridamole
Unit Price
৳ 10.00
28's pack৳ 280.00
(28's pack: ৳ 280.00)
UniMed UniHealth
Drug Class
Anti-platelet drugs
Indication
Transient ischemic attack
Dosage Form
Capsule (Modified Release)
Manufacturer
UniMed UniHealth
Clinical Information
Indication DetailsView
Dipyridamole is indicated in Prophylaxis of thromboembolism following cardiac valve replacement, Secondary prophylaxis of stroke or transient ischaemic attack
Therapeutic ClassView
Anti-platelet drugs
PharmacologyView
Dipyridamole causes an accumulation of adenosine, adenine nucleotides and cAMP by inhibiting the activity of adenosine deaminase and phosphodiesterase thus inhibiting platelet aggregation and may cause vasodilation.
DosageView
Prophylaxis of thromboembolism following cardiac valve replacement:
- Adult: 300-600 mg/day in divided doses with an oral anticoagulant.
- Child: 5 mg/kg/day in divided doses.
- Adult: As modified-release preparation: 200 mg bid, with or without aspirin.
AdministrationView
Should be taken on an empty stomach. Take 1 hr before meals. May be taken with meals to reduce GI discomfort.
Side EffectsView
GI disturbances, headache, dizziness, faintness, facial flushing, skin rash, liver dysfunction, angina. Large doses may lower BP.
ContraindicationsView
Hypersensitivity. Peptic ulcer.
PrecautionsView
In patients with rapidly worsening angina, subvalvular aortic stenosis, haemodynamic instability associated with recent MI or coagulation disorders esp when given IV during myocardial imaging. Hypotension, unstable angina, aortic stenosis. Pregnancy and lactation. Safety and efficacy are not established in childn < 12 yrs.
InteractionsView
Aminophylline may reverse vasodilatation effect. Useful combination with aspirin in prevention of thromboembolism. Efficacy reduced by concurrent admin of antacids. Concurrent use may increase the cardiotoxic effects of adenosine.
Pregnancy & LactationView
Pregnancy Category B. Either animal-reproduction studies have not demonstrated a fetal risk but there are no controlled studies in pregnant women or animal-reproduction studies have shown an adverse effect (other than a decrease in fertility) that was not confirmed in controlled studies in women in the 1st trimester (and there is no evidence of a risk in later trimesters).
Overdose EffectsView
Symptoms: warm feeling, flushes, sweating, restlessness, weakness, dizziness, hypotension and tachycardia.
Management: treatment is symptomatic. Empty stomach by gastric lavage. Haemodialysis unlikely to be useful.
Management: treatment is symptomatic. Empty stomach by gastric lavage. Haemodialysis unlikely to be useful.
Storage ConditionsView
Store below 25° C.