Image
Group 2336.png

Co-Tareg®

 

CoTareg is a combination medication used as an initial therapy for patients with hypertension who are likely to need multiple drugs to achieve their blood pressure goals. It combines valsartan, an angiotensin II receptor blocker (ARB), with hydrochlorothiazide, a thiazide diuretic.1

This combination works synergistically to lower blood pressure more effectively than either component alone.2

 

Co-Tareg for newly diagnosed Moderate hypertension1

Image
slide 5.gif

Co-tareg 160/12.5: greater sSBP and sDBP reductions of -32.1 mmHg and -16.9 mmHg were achieved in treatment naïve patients.4

Image
Group 2448.png

Study design4
17,242 patients were enrolled in an uncontrolled, multicenter observational study Regimen: Combined valsartan 160 mg and HCTZ 12.5 mg was prescribed according to the routine clinical practice of the physician in accordance with the Summary of Product Characteristics.
 

Objective4
To evaluate the effectiveness of this combination in achieving target BP levels

Image
Frame 427318816.png

Dosage and administration1

The recommended starting dose of CoTareg is 160 mg of valsartan and 12.5 mg of hydrochlorothiazide once daily. The maximum antihypertensive effect is typically seen within 2 to 4 weeks.

Image
Frame 427318817.png

Special considerations1

 

  • Renal Impairment: No dosage adjustment is required for patients with mild to moderate renal impairment (GFR ≥ 30 ml/min).

  • Hepatic Impairment: No dosage adjustment is required for patients with mild to moderate hepatic impairment. Due to the hydrochlorothiazide component, CoTareg should be used with particular caution in patients with severe hepatic impairment.

 

 

CV: Cardiovascular, GFR: Glomerular filtration rate.

SVG

Co-Tareg® API

PDF

References

  1. Egyptian drug authority Co-Tareg approved leaflet; approval date: 8/5/2025. 

  2. Summary of product characteristics. Co-diovan. Available at: https://www.ema.europa.eu/en/documents/referral/diovan-comp-article-30-referral-annex-i-ii-iii_en.pdf; last accessed: 2/7/2025.

  3. Mancia Chairperson G, Brunström M, Burnier M, Grassi G, Januszewicz A, Muiesan ML, Tsioufis K, Agabiti-Rosei E, Eae A, Azizi M, Benetos A. 2023 ESH Guidelines for the management of arterial hypertension The Task Force for the management of arterial hypertension of the European Society of Hypertension Endorsed by the European Renal Association (ERA) and the International Society of Hypertension (ISH). Journal of hypertension. 

  4. Abts M, Claus V, Lataster M. Blood pressure control with valsartan and hydrochlorothiazide in clinical practice: The MACHT Observational Study. Blood Pressure. 2006 Jan 1;15(sup1):27-32

Approved by Egyptian Drug Authority: HF0082OA4758/102025. Invalidation date: 14/10/2027.
Kindly report any violated online promotional, educational and awareness material not having this message to The General administration for Regulation of Marketing & Advertising Materials at: www.edaegypt.gov.eg.

Image
Valsartan QR.jpeg

HF0082OA4758/102025 14/10/2027

 

        

Adverse Events Reporting

We encourage using the following Electronic reporting tool for reporting into the safety database directly:
If the electronic reporting tool is not working - please use the following: https://www.report.novartis.com
1 - Generic Mailbox: [email protected]
2 - CISCO: +20 2 2 2861000: Press 3 for Adverse Events Reporting