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Nefrena Tablet

Nefrena Tablet

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Product Overview

Key Features

We are Trading and Supplying Nefrena Tablets in New Delhi, Delhi, India. A Renal Friendly Supplement.

I -Ketoanalogue Tablets

a cCalcium-3-methyl-2-oxo-valerate 67 mg
(I -ketoanalogue to isoleucine , calcium salt)
a cCalcium-4-methyl-2-oxo-valerate 101 mg
(I -ketoanalogue to leucine , calcium salt)
a cCalcium-2-oxo-3-phenylpropionate 68 mg
(I -ketoanalogue to phenylalanine , calcium salt)
a cCalcium-3-methyl-2-oxo-butyrate 86 mg
(I -ketoanalogue to valine , calcium salt)
a cCalcium-dl-2-hydroxy-4(methylthio) butyrate 59 mg
(I -hydroxyanalogue to methionine , calcium salt)
a cLysine acetate 105 mg (Eq to lysine 75 mg.)
a cL-threonine 53 mg
a cL-tryptophan 23 mg
a cL-histidine 38 mg
a cL-tyrosine 30 mg
a cTotal nitrogen content per tablet 36 mg
a cCalcium content per tablet 1.25 mmol=0.05 gm
Dietary protein restriction may improve determinants of CKD progression. However, the extent of improvement and effect of ketoanalogue supplementation are unclear. We conducted a prospective, randomized, controlled trial of safety and efficacy of ketoanaloguea supplemented vegetarian very lowa protein diet (KD) compared with conventional lowa protein diet (LPD). Primary end point was RRT initiation or >50% reduction in initial eGFR. Nondiabetic adults with stable eGFR<30 ml/min per 1.73 m2, proteinuria <1 g/g urinary creatinine, good nutritional status, and good diet compliance entered a run-in phase on LPD. After 3 months, compliant patients were randomized to KD (0.3 g/kg vegetable proteins and 1 cps/5 kg ketoanalogues per day) or continue LPD (0.6 g/kg per day) for 15 months. Only 14% of screened patients patients were randomized, with no differences between groups. Adjusted numbers needed to treat (NNTs; 95% confidence interval) to avoid composite primary end point in intention to treat and per-protocol analyses in one patient were 4.4 (4.2 to 5.1) and 4.0 (3.9 to 4.4), respectively, for patients with eGFR<30 ml/min per 1.73 m2. Adjusted NNT (95% confidence interval) to avoid dialysis was 22.4 (21.5 to 25.1) for patients with eGFR<30 ml/min per 1.73 m2 but decreased to 2.7 (2.6 to 3.1) for patients with eGFR<20 ml/min per 1.73 m2 in intention to treat analysis. Correction of metabolic abnormalities occurred only with KD. Compliance to diet was good, with no changes in nutritional parameters and no adverse reactions. Thus, this KD seems nutritionally safe and could defer dialysis initiation in some patients with CKD - Journal of the American Society of Nephrology.

Company Details

Know Us To meet the demands of medicines, we, Aar Ess Remedies Pvt Ltd., have emerged as a reliable business entity in this industry. Since then, we have managed to maintain high standards in our products at competitive prices. With immense knowledge and rich experience, we have acquired a prominent position of one of the noted traders & suppliers in this competitive industry. 38367_ 38367_HOME2.jpg Banking on valuable contribution of reliable manufacturers and efficient workforce, we are able to show case a quality range of products such as Pharmaceutical

Business Type

Supplier, Trading Company

Employee Count

30

Establishment

2003

Working Days

Monday To Sunday

GST NO

07AAECA9312Q1ZA

Seller Details

AAR ESS REMEDIES PVT. LTD.

AAR ESS REMEDIES PVT. LTD.

GST

07AAECA9312Q1ZA

DIRECTOR

Mr Sandeep Sharma

Member Since

8 Years

AddressView on Map

Wz 13e, Lane No.4, Vashisth Park, Pankha Road, New Delhi, Delhi, 110046, India

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