GOPRIL ( TABLET ) ( 2.5 mg )

Manufacturer
CMG Biotech
Drug Type
 Branded Drug
Medicine System
 Allopathy
Drug Availability
 Pharmacy (P)

Ingredients

SKU

Brand NameDosage Form PackQty per PackInquiry
GOPRILTABLET1 Please Inquire

Related Generic Drugs

Related Monographs

Ramipril

Pregnancy Category D

Schedule Drug Category: H

Dosage

Source : IAP Pediatric Drug Formulary
Hypertension and proteinuria in chronal renal disease.

Source : NFI National Formulary of India
Oral

  • Children - 1.5 mg/m2/24 h once daily. Adolescents-2.5 mg once daily. Adjust dosage to achieve proper blood pressure response, up to max of 20 mg/day. But more studies are required in children before it is used in pediatrics.
Reduction in risk of myocardial infarction, stroke, and death from cardiovascular causes:
Initial dose of 2.5 mg, once a day for 1 week, 5 mg, once a day for the next 3 weeks, and then increased as tolerated, to a maintenance dose of 10 mg once a day.
Hypertension: The recommended initial dose for patients not receiving a diuretic is 2.5 mg once a day. The usual maintenance dosage range is 2.5 to 20 mg per day administered as a single dose or in two equally divided doses.
Heart failure post myocardial infarction: Initial dose is 2.5 mg twice daily, after one week at the starting dose titrate to ( if tolerated) toward a target dose of 5 mg twice daily, with dosage increases being about 3 weeks apart.

Usage / Indications

  • Reduction in risk of myocardial infarction, stroke and death from cardiovascular causes
  • Hypertension
  • Heart failure post myocardial infarction.

Contraindications

Hypersensitivity to ramipril or any other ACE inhibitor, bilateral renal artery stenosis or a single kidney with unilateral renal artery stenosis.

Precautions

  • Impaired renal function, impaired liver function, diabetes mellitus (increased risk of hyperkalemia), patients undergoing surgery, history of angioedema
  • Symptomatic hypotension is most likely to occur in patients who have been volume- and/or salt-depleted as a result of prolonged diuretic therapy, dietary salt restriction, dialysis, diarrhoea, or vomiting. Volume and/or salt depletion should be corrected before initiating therapy.
  • Monitoring of white blood cell counts should be considered in patients with collagen- vascular disease, especially if the disease is associated with impaired renal function.
  • Administration during pregnancy can cause fetal/neonatal morbidity and death.
  • When pregnancy is detected ACE inhibitors should be discontinued as soon as possible, interactions.

Side Effects / Adverse Effects

Hypotension, cough, asthenia, dizziness, headache, angioneurotic edema, hypersensitivity reactions, erythema multiforme, toxic epidermal necrolysis, Stevens Johnson syndrome, hepatic necrosis, pancreatitis, pancytopenia, thrombocytopenia.

Storage

Store protected from moisture at a  temperature not exceeding 300C.

Disclaimer:

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