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Collaborative and Other Relationships (Details) (USD $)
3 Months Ended 12 Months Ended
Dec. 31, 2012
Sep. 30, 2012
Jun. 30, 2012
Mar. 31, 2012
Dec. 31, 2011
Sep. 30, 2011
Jun. 30, 2011
Mar. 31, 2011
Dec. 31, 2012
Dec. 31, 2011
Dec. 31, 2010
Revenues from unconsolidated joint business                      
Revenue on sales of RITUXAN in the rest of world $ 1,074,700,000 [1],[2] $ 1,039,100,000 $ 1,076,800,000 [3] $ 975,400,000 [4] $ 996,600,000 [5] $ 975,800,000 $ 956,700,000 [6] $ 907,100,000 $ 4,166,074,000 $ 3,836,117,000 $ 3,470,056,000
Total unconsolidated joint business revenues 280,900,000 [1],[2] 287,800,000 284,600,000 [3] 284,600,000 [4] 257,500,000 [5] 266,500,000 216,500,000 [6] 256,100,000 1,137,923,000 996,597,000 1,077,244,000
U.S
                     
Revenues from unconsolidated joint business                      
Revenue on sales of RITUXAN in the rest of world                 2,176,800,000 1,954,800,000 1,744,400,000
Roche Group - Genentech
                     
Revenues from unconsolidated joint business                      
Total unconsolidated joint business revenues                 1,137,900,000 996,600,000 1,077,200,000
Roche Group - Genentech | U.S
                     
Revenues from unconsolidated joint business                      
Biogen Idec's share of pre-tax co-promotion profits in the U.S                 1,031,700,000 872,700,000 848,000,000
Reimbursement of our selling and development expenses in the U.S                 1,600,000 6,100,000 58,300,000
RITUXAN
                     
Co-promotion profit sharing formula                      
First $50.0 million 30.00%               30.00%    
Above $50.0 million 40.00%       40.00%       40.00% 40.00% 40.00%
RITUXAN | Roche Group - Genentech | Outside the U.S
                     
Revenues from unconsolidated joint business                      
Revenue on sales of RITUXAN in the rest of world                 $ 104,600,000 $ 117,800,000 $ 170,900,000
RITUXAN | After First New Product FDA Approval
                     
Co-promotion profit sharing formula                      
First $50.0 million 30.00%               30.00%    
Above $50.0 million 0.00%               0.00%    
Until First GA101 Threshold Date 38.00%               38.00%    
After First GA101 Threshold Date                      
Until First Threshold Date 37.50%               37.50%    
After First Threshold Date and until Second Threshold Date 35.00%               35.00%    
After Second Threshold Date 30.00%               30.00%    
Until Second GA101 Threshold Date 0.00%               0.00%    
After Second GA101 Threshold Date 0.00%               0.00%    
First Non CLL GA 101 FD Approval Occurs First | RITUXAN | Before First New Product FDA Approval
                     
Co-promotion profit sharing formula                      
First $50.0 million 30.00%               30.00%    
Above $50.0 million 0.00%               0.00%    
Until First GA101 Threshold Date 39.00%               39.00%    
After First GA101 Threshold Date                      
Until First Threshold Date 0.00%               0.00%    
After First Threshold Date and until Second Threshold Date 0.00%               0.00%    
After Second Threshold Date 0.00%               0.00%    
Until Second GA101 Threshold Date 37.50%               37.50%    
After Second GA101 Threshold Date 35.00%               35.00%    
GA 101 CLL Sales Trigger Occurs First | RITUXAN | Before First New Product FDA Approval
                     
Co-promotion profit sharing formula                      
First $50.0 million 30.00%               30.00%    
Above $50.0 million 35.00%               35.00%    
Until First GA101 Threshold Date 0.00%               0.00%    
After First GA101 Threshold Date                      
Until First Threshold Date 0.00%               0.00%    
After First Threshold Date and until Second Threshold Date 0.00%               0.00%    
After Second Threshold Date 0.00%               0.00%    
Until Second GA101 Threshold Date 0.00%               0.00%    
After Second GA101 Threshold Date 0.00%               0.00%    
[1] Net income and net income attributable to Biogen Idec Inc. for the fourth quarter of 2012 includes a charge to research and development expense of $30.0 million related to an upfront payment made in connection with our development agreement entered into with Isis Pharmaceuticals, Inc.
[2] Net income and net income attributable to Biogen Idec Inc. for the fourth quarter of 2012 includes the correction of an error that had accumulated over several prior years in our deferred tax accounting for capitalized interest which resulted in an expense of $29.0 million.
[3] Net income and net income attributable to Biogen Idec Inc. for the second quarter of 2012 includes a charge to research and development expense of $12.0 million related to an upfront payment made in connection with our development agreement entered into with Isis Pharmaceuticals, Inc.
[4] Net income and net income attributable to Biogen Idec Inc. for the first quarter of 2012 includes a charge to research and development expense of $29.0 million related to an upfront payment made in connection with our development agreement entered into with Isis Pharmaceuticals, Inc. and a $12.4 million reduction resulting from an increase in our returns reserve and write-offs of unsold inventory due to a voluntary withdrawal of a limited amount of AVONEX product that has demonstrated a trend in oxidation that may lead to expiry earlier than stated on its label.
[5] Net income and net income attributable to Biogen Idec Inc. for the fourth quarter of 2011 includes a charge to research and development expense of $36.8 million related to an upfront payment made in connection with our collaboration and license agreement entered into with Portola Pharmaceuticals, Inc.
[6] Our share of RITUXAN revenues from unconsolidated joint business was reduced by approximately $50.0 million in the second quarter of 2011 as a result of an accrual for estimated compensatory damages (including interest) relating to Genentech’s ongoing arbitration with Hoechst GmbH. For additional information related to this matter, please read Note 22, Litigation to these consolidated financial statements.