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POWER
MEETS
SYNERGY
Synjardy® INDICATED to improve
glycemic control and reduce the risk of
cardiovascular death in adults with T2D
& established cardiovascular diseases 1
Available as:
5mg/500mg, 5mg/850mg, 5mg/1000mg,
12.5mg/500mg, 12.5mg/850mg,
12.5mg/1000mg
RRR
Relative risk reduction in CV death - HbA1c REDUCTION
Results from EMPA REG OUTCOME® trial 1,2
Synjardy® effectively lowers HbA1c up to 4.6% 3
Absolute Risk Reduction 2.2%
®
Jardiance recommended
80 Guideline Recommendations to reduce the risk of Cardiovascular
by SEMDSA
More than 80 standard guidelines across
the globe has incorporated evidence from death in Type 2 Diabetes patients with
established cardiovascular disease.
EMPA-REG outcome. 4
References: 1. Synjardy approved prescribing information, Boehringer Ingelheim 2020. 2. Zinman B, Wanner C, Lachin JM, et al; EMPA-REG OUTCOME Investigators. Empagliflozin,
®
®
cardiovascular outcomes, and mortality in type 2 diabetes. N Engl J Med. 2015;373(22):2117-2128. 3. Hadjadj S, et al. Diabetes Care 2016; 2016 Oct;39(10):1718-28. doi: 10.2337/dc16-0522.
4. Boehringer Ingelheim data on file.
Synjardy is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve
®
glycaemic control - in patients inadequately controlled on their maximally tolerated dose of metformin alone - in patients inadequately
controlled with metformin in combination with other glucose-lowering medicine.
For full prescribing information refer to the professional information approved by the Regulatory Authority. Applicant details: Ingelheim Pharmaceuticals (Pty)
Ltd, 407 Pine Ave, Randburg. Tel: +27 (011) 348-2400. Cpy. Reg. No. 1966/008618/07. BI Ref. No. PC-ZA-101048. Expiry date: March 2023.