THIRD QUARTER AND NINE MONTHS RESULTS 2009


THIRD QUARTER AND NINE MONTHS RESULTS 2009

Third quarter revenue increased by 10 percent at constant exchange rates (CER)
to $8,200 million.

-US sales of Toprol-XL, benefiting from withdrawal of generic products,
accounted for 3 percent of global revenue growth at CER. 
-US sales of Novel Influenza A (H1N1) vaccine totalled $152 million in the third
quarter, accounting for 2 percent of global revenue growth at CER. 
-Emerging Markets revenue was up 15 percent at CER; on track for double-digit
growth for the full year.

Core operating profit in the third quarter increased by 29 percent at CER to
$3,609 million on revenue growth and operational efficiencies.  
 
Core EPS in the third quarter increased by 27 percent at CER to $1.68. 

Reported EPS in the third quarter increased by 22 percent at CER to $1.46. 
  
-Agreement in principle reached with the US Attorney's Office in Philadelphia to
resolve its investigations related to Seroquel sales and marketing practices.
This accounts for $520 million of the $538 million provisions taken in the first
nine months, $108 million of which taken in third quarter (see Note 4).

Strong cash flows have reduced net debt by $3,981 million since 31 December
2008.

Pipeline developments include:
-New diabetes treatment ONGLYZATM approved in the US and the European Union.
-Brilinta submitted for regulatory approval in the European Union; on track for
US submission in the fourth quarter.
-New late stage development collaborations announced with Forest Laboratories
and Nektar Therapeutics.
-Regulatory submissions for Zactima have been withdrawn, based upon an updated
analysis that demonstrated no overall survival advantage when added to
chemotherapy.

Core EPS target for the full year increased to range of $6.20 to $6.40. 

Financial Summary
 					
[See PDF for table]

David Brennan, Chief Executive Officer, said:  “Our strong business performance
is driven by good operating execution bolstered by revenue upsides from
Toprol-XL and H1N1 vaccine sales.  All these factors are reflected in our
results for the first nine months and our increased Core EPS target for the full
year.  Since the half year we have made progress on the pipeline with the
approval of ONGLYZATM, the European submission for Brilinta and new external
collaborations, tempered by the disappointing news on Zactima.”

Media Enquiries:	
Neil McCrae (London) (020) 7304 5045
Chris Sampson/Sarah Lindgreen (London) (020) 7304 5130/5033
Tony Jewell (Wilmington) (302) 885 4594
Ann-Leena Mikiver (Södertälje) (8) 553 260 20
		
Analyst/Investor Enquiries	
Karl Hård (London)	(020) 7304 5322
Jonathan Hunt (London) (020) 7304 5087
Ed Seage/Jörgen Winroth (US) (302) 886 4065/(212) 579 0506

Attachments

Q3_figures_Final_29_Oct.pdf 10292261.pdf