Summary |
|||
|
|||
■ |
Broadly-based sales growth with Group turnover +1% CER: |
||
|
- |
Pharmaceuticals and Vaccines sales flat: US +2%, Europe +5%, Japan +2% offset by EMAP -9%, impacted by decline in China sales and Vaccines phasing |
|
|
- |
Consumer Healthcare +4% |
|
|
- |
Total Group turnover ex-divestments +1% |
|
|
|
||
■ |
Further significant pipeline approvals and filings: |
||
|
- |
4 approvals; US: Tivicay for HIV and FluLaval Q-IV vaccine for flu; Europe: Tafinlar for metastatic melanoma; Japan: Relvar Ellipta for asthma |
|
|
- |
Positive FDA Adcom recommendation for Anoro Ellipta in COPD and positive CHMP opinion for Relvar Ellipta in asthma & COPD |
|
|
- |
3 FDA filings: Arzerra for first-line CLL; dolutegravir-Trii for HIV; fluticasone furoate monotherapy for asthma |
|
|
|
||
■ |
Continued delivery of operating and financial efficiencies, strong cash generation and returns to shareholders: |
||
|
- |
Net cash inflow from operating activities of £2.1 billion; core tax rate 23.5% |
|
|
- |
Core EPS 28.9p (+16%) benefiting from operating, financial and long-term cost efficiencies |
|
|
- |
Q3 dividend: 19p (+6%) |
|
|
- |
£1 billion of shares repurchased by the end of Q3; continue to target £1-2 billion for the year |
|
|
|
|
|
■ |
Successful implementation of measures to drive strategic focus and improve growth outlook: |
||
|
- |
Agreement to divest Lucozade and Ribena to Suntory for £1.35 billion and Arixtra/Fraxiparine and related manufacturing site to Aspen for £700 million |
|
|
|
||
■ |
Full year 2013 guidance reaffirmed: |
||
|
- |
Core EPS growth of 3-4% on sales growth of around 1% (both CER) |