Abbott Laboratories (ABT), (founding name: Abbott Alkaloid Company) is a global pharmaceutical company with around 73,000 employees in 150 countries. Abbott was founded in 1888 by Wallace C. Abbott (1857-1921) and is headquartered in Abbott Park, a northern suburb of Chicago, Illinois.
Table of Contents
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 10-Q
(Mark One)
x QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended March 31, 2014
OR
o TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from to
Commission File No. 1-2189
ABBOTT LABORATORIES
An Illinois Corporation
I.R.S. Employer Identification No.
36-0698440
100 Abbott Park Road
Abbott Park, Illinois 60064-6400
Telephone: (847) 937-6l00
Indicate by check mark whether the registrant: (l) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of l934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes x No o
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 229.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes x No o
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of large accelerated filer, accelerated filer and smaller reporting company in Rule 12b-2 of the Exchange Act. (Check one):
Large Accelerated Filer x
Accelerated Filer o
Non-Accelerated Filer o
Smaller reporting company o
(Do not check if a smaller reporting company)
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes o No x
As of March 31, 2014, Abbott Laboratories had 1,501,938,538 common shares without par value outstanding.
Abbott Laboratories
Page
Part I - Financial Information
Item 1. Financial Statements and Supplementary Data
Condensed Consolidated Statement of Earnings
3
Condensed Consolidated Statement of Comprehensive Income
4
Condensed Consolidated Balance Sheet
5
Condensed Consolidated Statement of Cash Flows
6
Notes to Consolidated Financial Statements
7
Item 2. Managements Discussion and Analysis of Financial Condition and Results of Operations
15
Item 4. Controls and Procedures
18
Part II - Other Information
Item 1. Legal Proceedings
19
Item 2. Unregistered Sales of Equity Securities and Use of Proceeds
Item 6. Exhibits
Signature
20
2
Abbott Laboratories and Subsidiaries
(Unaudited)
(dollars in millions except per share data; shares in thousands)
Three Months Ended March 31
2014
2013
Net sales
$
5,244
5,378
Cost of products sold, excluding amortization of intangible assets
2,470
2,432
Amortization of intangible assets
174
199
Research and development
387
346
Selling, general and administrative
1,762
1,786
Total operating cost and expenses
4,793
4,763
Operating earnings
451
615
Interest expense
39
41
Interest (income)
(16
)
(15
Net foreign exchange loss (gain)
29
Other (income) expense, net
Earnings from continuing operations before taxes
423
554
Taxes on earnings from continuing operations
84
10
Earnings from continuing operations
339
544
Earnings from discontinued operations, net of tax
36
Net Earnings
375
Basic Earnings Per Common Share
Continuing operations
0.22
0.35
Discontinued operations
0.02
Net earnings
0.24
Diluted Earnings Per Common Share
0.34
Cash Dividends Declared Per Common Share
0.14
Average Number of Common Shares Outstanding Used for Basic Earnings Per Common Share
1,532,810
1,568,730
Dilutive Common Stock Options and Awards
14,881
17,288
Average Number of Common Shares Outstanding Plus Dilutive Common Stock Options and Awards
1,547,691
1,586,018
Outstanding Common Stock Options Having No Dilutive Effect
4,421
5,518
The accompanying notes to condensed consolidated financial statements are an integral part of this statement.
(dollars in millions)
Less: Earnings from discontinued operations
Foreign currency translation (loss) gain adjustments
62
(391
Net actuarial gains (losses) and amortization of net actuarial (losses) and prior service (cost) and credits, net of taxes of $8 in 2014 and $(26) in 2013
16
(41
Unrealized gains on marketable equity securities, net of taxes of $0 in 2014 and 2013
1
Net adjustments for derivative instruments designated as cash flow hedges, net of taxes of $0 in 2014 and $(5) in 2013
(21
Other comprehensive income (loss) from continuing operations
78
(452
Comprehensive income from continuing operations
417
92
Comprehensive income from discontinued operations
Comprehensive Income
453
March 31,
December 31,
Supplemental Accumulated Other Comprehensive Income (Loss) Information, net of tax:
Cumulative foreign currency translation (loss) adjustments
(656
(718
Net actuarial (losses) and prior service (cost) and credits
(1,296
(1,312
Cumulative unrealized gains on marketable equity securities
13
Cumulative gains on derivative instruments designated as cash flow hedges
March 31, 2014
December 31, 2013
Assets
Current Assets:
Cash and cash equivalents
2,060
3,475
Investments, primarily bank time deposits and U.S. treasury bills
4,987
4,623
Trade receivables, less allowances of $324 in 2014 and $312 in 2013
3,883
3,986
Inventories:
Finished products
1,921
1,866
Work in process
322
349
Materials
532
478
Total inventories
2,775
2,693
Prepaid expenses, deferred income taxes, and other receivables
3,977
4,032
Current assets held for disposition
249
438
Total Current Assets
17,931
19,247
Investments
122
119
Property and equipment, at cost
13,005
12,870
Less: accumulated depreciation and amortization
7,057
6,965
Net property and equipment
5,948
5,905
Intangible assets, net of amortization
5,613
5,735
Goodwill
9,781
9,772
Deferred income taxes and other assets
2,214
2,109
Non-current assets held for disposition
53
66
41,662
42,953
Liabilities and Shareholders Investment
Current Liabilities:
Short-term borrowings
4,370
3,164
Trade accounts payable
1,074
1,026
Salaries, wages and commissions
681
906
Other accrued liabilities
3,401
3,500
Dividends payable
331
341
Income taxes payable
152
175
Current portion of long-term debt
8
9
Current liabilities held for disposition
169
386
Total Current Liabilities
10,186
9,507
Long-term debt
3,387
3,388
Post-employment obligations, deferred income taxes and other long-term liabilities
4,599
4,784
Non-current liabilities held for disposition
Commitments and Contingencies
Shareholders Investment:
Preferred shares, one dollar par value Authorized 1,000,000 shares, none issued
Common shares, without par value Authorized - 2,400,000,000 shares
Issued at stated capital amount - Shares: 2014: 1,689,594,829; 2013: 1,685,827,096
12,032
12,048
Common shares held in treasury, at cost - Shares: 2014: 187,656,291; 2013: 137,728,810
(8,713
(6,844
Earnings employed in the business
22,005
21,979
Accumulated other comprehensive income (loss)
(1,934
(2,012
Total Abbott Shareholders Investment
23,390
25,171
Noncontrolling Interests in Subsidiaries
99
96
Total Shareholders Investment
23,489
25,267
Cash Flow From (Used in) Operating Activities:
Adjustments to reconcile earnings to net cash from operating activities -
Depreciation
224
222
Amortization of intangibles
Share-based compensation
126
Trade receivables
82
(10
Inventories
(90
(132
Other, net
(548
(489
Net Cash From Operating Activities
336
460
Cash Flow From (Used in) Investing Activities:
Acquisitions of property and equipment
(255
(274
Purchases of investment securities, net
(367
(1,834
Other
27
Net Cash (Used in) Investing Activities
(595
(2,108
Cash Flow From (Used in) Financing Activities:
Proceeds from issuance of short-term debt and other
1,213
2,248
Transfer of cash and cash equivalents to AbbVie Inc.
(5,901
Purchases of common shares
(2,192
(925
Proceeds from stock options exercised, including income tax benefit
170
69
Dividends paid
(343
(224
Net Cash (Used in) Financing Activities
(1,152
(4,733
Effect of exchange rate changes on cash and cash equivalents
(4
(48
Net Decrease in Cash and Cash Equivalents
(1,415
(6,429
Cash and Cash Equivalents, Beginning of Year
10,802
Cash and Cash Equivalents, End of Period
4,373
Notes to Condensed Consolidated Financial Statements
Note 1 Basis of Presentation
The accompanying unaudited, condensed consolidated financial statements have been prepared pursuant to rules and regulations of the Securities and Exchange Commission and, therefore, do not include all information and footnote disclosures normally included in audited financial statements. However, in the opinion of management, all adjustments (which include only normal adjustments) necessary to present fairly the results of operations, financial position and cash flows have been made. It is suggested that these statements be read in conjunction with the financial statements included in Abbotts Annual Report on Form 10-K for the year ended December 31, 2013. The consolidated financial statements include the accounts of the parent company and subsidiaries, after elimination of intercompany transactions.
Note 2 Separation of AbbVie Inc.
On January 1, 2013, Abbott completed the separation of AbbVie Inc. (AbbVie), which was formed to hold Abbotts research-based proprietary pharmaceuticals business. Abbott and AbbVie entered into transitional services agreements prior to the separation pursuant to which Abbott and AbbVie are providing to each other, on an interim transitional basis, various services. Transition services may be provided for up to 24 months with an option for a one-year extension by the recipient. Services being provided by Abbott include certain information technology and back office support. Billings by Abbott under these transitional services agreements are recorded as a reduction of the costs to provide the respective service in the applicable expense category in the Condensed Consolidated Statement of Earnings. This transitional support will enable AbbVie to establish its stand-alone processes for various activities that were previously provided by Abbott and does not constitute significant continuing support of AbbVies operations.
For a small portion of AbbVies operations, the legal transfer of AbbVies assets (net of liabilities) did not occur with the separation of AbbVie on January 1, 2013 due to the time required to transfer marketing authorizations and other regulatory requirements in each of these countries. Under the terms of the separation agreement with Abbott, AbbVie is subject to the risks and entitled to the benefits generated by these operations and assets. The majority of these operations were transferred to AbbVie in 2013 with the remainder expected to be transferred in 2014. These assets and liabilities have been presented as held for disposition in the Condensed Consolidated Balance Sheet. At March 31, 2014, the assets and liabilities held for disposition consist of trade accounts receivable of $127 million, inventories of $102 million, equipment of $17 million, other assets of $56 million, trade accounts payable and accrued liabilities of $152 million and other liabilities of $18 million. Abbotts obligation to transfer the net assets held for disposition to AbbVie of $132 million is included in Other accrued liabilities.
Abbott has retained all liabilities for all U.S. federal and foreign income taxes on income prior to the separation, as well as certain non-income taxes attributable to AbbVies business. AbbVie generally will be liable for all other taxes attributable to its business.
Earnings from discontinued operations in the first quarter of 2014 reflect the recognition of $36 million of net tax benefits primarily as a result of the resolution of various tax positions related to AbbVies operations for years prior to the separation.
Note 3 Supplemental Financial Information
Shares of unvested restricted stock that contain non-forfeitable rights to dividends are treated as participating securities and are included in the computation of earnings per share under the two-class method. Under the two-class method, net earnings are allocated between common shares and participating securities. Earnings from Continuing Operations allocated to common shares for the three months ended March 31, 2014 and 2013 were $337 million and $541 million, respectively. Net earnings allocated to common shares for the three months ended March 31, 2014 and 2013 were $373 million and $541 million, respectively.
Other, net use of cash in Net cash from operating activities in the Condensed Consolidated Statement of Cash Flows for the first three months of 2014 and 2013 includes the effects of contributions to defined benefit plans of $312 million and $208 million, respectively, and to the post-employment medical and dental benefit plans of $40 million in each quarter, as well as the non-cash impact in the first quarter of 2014 of approximately $110 million of tax benefits from the resolution of various tax positions pertaining to prior years.
The components of long-term investments as of March 31, 2014 and December 31, 2013 are as follows:
Equity securities
91
93
31
26
Total
Note 4 Other Comprehensive Income
The components of the changes in other comprehensive income from continuing operations, net of income taxes, are as follows:
Cumulative Foreign Currency Translation Adjustments
Net Actuarial Losses and Prior Service Costs and Credits
Cumulative Unrealized Gains on Marketable Equity Securities
Cumulative Gains on Derivative Instruments Designated as Cash Flow Hedges
(in millions)
Balance at December 31, 2013 and 2012
(79
(3,596
50
Separation of AbbVie (a)
(307
1,451
Other comprehensive income before reclassifications
(69
(1
(18
Amounts reclassified from accumulated other comprehensive income (a)
28
(6
(3
Net current period comprehensive income from continuing operations
Balance at March 31
(777
(2,186
32
38
(a) Prior year amounts have been appropriately revised to reflect a reclassification between Cumulative foreign currency translation adjustment and Net actuarial losses and prior service costs and credits.
(b) Reclassified amounts for foreign currency translation are recorded in the Condensed Consolidated Statement of Earnings as Net foreign exchange loss (gain); gains on marketable equity securities as Other (income) expense, net and cash flow hedges as Cost of products sold. Net actuarial losses and prior service cost is included as a component of net periodic benefit plan costs; see Note 11 for additional details.
Note 5 Business Acquisitions
In August 2013, Abbott acquired 100 percent of IDEV Technologies, net of debt, for $310 million, in cash. The acquisition of IDEV Technologies expands Abbotts endovascular portfolio. The final allocation of the fair value at the date of acquisition resulted in non-deductible acquired in-process research and development of approximately $170 million which is accounted for as an indefinite-lived intangible asset until regulatory approval or discontinuation; non-deductible definite-lived intangible assets of approximately $66 million; non-deductible goodwill of approximately $112 million; and net deferred tax liabilities of $47 million. Acquired intangible assets consist of developed technology and are being amortized over 11 years.
In August 2013, Abbott acquired 100 percent of OptiMedica for $260 million, in cash, plus additional payments up to $150 million to be made upon completion of certain development, regulatory and sales milestones. The acquisition of OptiMedica provides Abbott with an immediate entry point into the laser assisted cataract surgery market. The final allocation of the fair value at the date of acquisition resulted in non-deductible definite-lived intangible assets of approximately $160 million; non-deductible acquired in-process research and development of approximately $60 million which is accounted for as an indefinite-lived intangible asset until regulatory approval or discontinuation; non-deductible goodwill of approximately $130 million; net deferred tax liabilities of $49 million; and contingent consideration of approximately $70 million. The fair value of the contingent consideration was determined based on an independent appraisal. Acquired intangible assets consist of developed technology and are being amortized over 18 years.
Note 6 Goodwill and Intangible Assets
The total amount of goodwill reported was $9.781 billion at March 31, 2014 and $9.772 billion at December 31, 2013. Foreign currency translation adjustments increased goodwill by approximately $35 million, while purchase price allocation adjustments associated with recent acquisitions decreased goodwill by approximately $26 million. The amount of goodwill related to reportable segments at March 31, 2014 was $3.0 billion for the Established Pharmaceutical Products segment, $286 million for the Nutritional Products segment, $444 million for the Diagnostic Products segment, and $3.1 billion for the Vascular Products segment. There was no reduction of goodwill relating to impairments.
The gross amount of amortizable intangible assets, primarily product rights and technology was $12.4 billion as of March 31, 2014 and $12.2 billion as of December 31, 2013, and accumulated amortization was $6.9 billion as of March 31, 2014 and $6.8 billion as of December 31, 2013. Indefinite-lived intangible assets, which relate to in-process research and development acquired in a business combination, was approximately $114 million at March 31, 2014 and $266 million at December 31, 2013. The change reflects the movement of an IDEV-related intangible asset, Supera, to amortizable assets due to the receipt of regulatory approval in the first quarter of 2014. Abbotts estimated annual amortization expense for intangible assets is approximately $655 million in 2014, $615 million in 2015, $590 million in 2016, $575 million in 2017 and $500 million in 2018. Amortizable intangible assets are amortized over 2 to 20 years (weighted average 11 years).
Note 7 Restructuring Plans
In the first quarter of 2014, Abbott management approved plans to streamline various operations in order to reduce costs and improve efficiencies in Abbotts vascular, diagnostics and nutritional businesses. Abbott recorded employee related severance and other charges of approximately $80 million in 2014. Approximately $17 million is recognized in Cost of products sold, $41 million is recognized in Research and development and approximately $22 million is recognized in Selling, general and administrative expense. The following summarizes the activity for these restructurings:
Restructuring charges recorded in 2014
80
Payments and other adjustments
Accrued balance at March 31, 2014
76
In 2014 and 2013, Abbott management approved plans to reduce costs and improve efficiencies across various functional areas. In 2013, Abbott management also approved plans to streamline certain manufacturing operations in order to reduce costs and improve efficiencies in Abbotts established pharmaceuticals business. In 2012, Abbott management approved plans to streamline various commercial operations in order to reduce costs and improve efficiencies in Abbotts core diagnostics, established pharmaceuticals and nutritionals businesses. Additional charges of approximately $25 million were recognized in 2014 of which approximately $2 million is recorded in Cost of products sold and approximately $23 million as Selling, general and administrative expense. The following summarizes the activity for the first three months of 2014 related to these restructuring actions and the status of the related accrual as of March 31, 2014:
Accrued balance at December 31, 2013
148
25
(28
145
In 2013 and prior years, Abbott management approved plans to realign its vascular manufacturing operations in order to reduce costs. The following summarizes the activity for the first three months of 2014 related to these restructuring actions and the status of the related accrual as of March 31, 2014:
In 2011 and 2008, Abbott management approved plans to streamline global manufacturing operations, reduce overall costs, and improve efficiencies in Abbotts core diagnostics business. The following summarizes the activity for the first three months of 2014 related to these restructuring actions and the status of the related accrual as of March 31, 2014:
Note 8 Incentive Stock Programs
In the first three months of 2014, Abbott granted 3,659,969 stock options, 545,716 restricted stock awards and 5,248,937 restricted stock units under its incentive stock programs. At March 31, 2014, approximately 110 million shares were reserved for future grants. Information regarding the number of options outstanding and exercisable at March 31, 2014 is as follows:
Outstanding
Exercisable
Number of shares
42,297,580
34,724,241
Weighted average remaining life (years)
4.5
3.5
Weighted average exercise price
27.34
25.38
Aggregate intrinsic value (in millions)
480
461
The total unrecognized share-based compensation cost at March 31, 2014 amounted to approximately $264 million which is expected to be recognized over the next three years.
Note 9 Financial Instruments, Derivatives and Fair Value Measures
Certain Abbott foreign subsidiaries enter into foreign currency forward exchange contracts to manage exposures to changes in foreign exchange rates for anticipated intercompany purchases by those subsidiaries whose functional currencies are not the U.S. dollar. These contracts, with notional amounts totaling $275 million and $137 million at March 31, 2014 and December 31, 2013, respectively, are designated as cash flow hedges of the variability of the cash flows due to changes in foreign exchange rates and are recorded at fair value. Accumulated gains and losses as of March 31, 2014 will be included in Cost of products sold at the time the products are sold, generally through the next twelve months. The amount of hedge ineffectiveness was not significant in 2014 and 2013.
Abbott enters into foreign currency forward exchange contracts to manage currency exposures for foreign currency denominated third-party trade payables and receivables, and for intercompany loans and trade accounts payable where the receivable or payable is denominated in a currency other than the functional currency of the entity. For intercompany loans, the contracts require Abbott to sell or buy foreign currencies, primarily European currencies and Japanese yen, in exchange for primarily U.S. dollars and other European currencies. For intercompany and trade payables and receivables, the currency exposures are primarily the U.S. dollar, European currencies and Japanese yen. At March 31, 2014 and December 31, 2013, Abbott held $11.8 billion and $13.8 billion, respectively, of such foreign currency forward exchange contracts.
Abbott has designated foreign denominated short-term debt as a hedge of the net investment in a foreign subsidiary of approximately $516 million and approximately $505 million as of March 31, 2014 and December 31, 2013, respectively. Accordingly, changes in the reported value of this debt due to changes in exchange rates are recorded in Accumulated other comprehensive income (loss), net of tax.
Abbott is a party to interest rate swap contracts totaling approximately $1.5 billion at March 31, 2014 and $1.5 billion at December 31, 2013 to manage its exposure to changes in the fair value of fixed-rate debt. These contracts are designated as fair value hedges of the variability of the fair value of fixed-rate debt due to changes in the long-term benchmark interest rates. The effect of the hedge is to change a fixed-rate interest obligation to a variable rate for that portion of the debt. Abbott records the contracts at fair value and adjusts the carrying amount of the fixed-rate debt by an offsetting amount. No hedge ineffectiveness was recorded in income in 2014 or 2013 for these hedges.
The following table summarizes the amounts and location of certain derivative financial instruments as of March 31, 2014 and December 31, 2013:
Fair Value - Assets
Fair Value - Liabilities
Dec. 31, 2013
Balance Sheet Caption
Interest rate swaps designated as fair value hedges
98
87
Foreign currency forward exchange contracts:
Hedging instruments
14
Others not designated as hedges
40
70
56
75
Debt designated as a hedge of net investment in a foreign subsidiary
n/a
516
505
147
171
572
580
The following table summarizes the activity for foreign currency forward exchange contracts designated as cash flow hedges, debt designated as a hedge of net investment in a foreign subsidiary and the amounts and location of income (expense) and gain (loss) reclassified into income in the first three months of 2014 and 2013 and for certain other derivative financial instruments. The amount of hedge ineffectiveness was not significant in 2014 and 2013 for these hedges.
Gain (loss) Recognized in Other Comprehensive Income (loss)
Income (expense) and Gain (loss) Reclassified into Income
Income Statement Caption
Foreign currency forward exchange contracts designated as cash flow hedges
17
Cost of products sold
(11
11
Foreign currency forward exchange contracts not designated as a hedge
(13
90
The interest rate swaps are designated as fair value hedges of the variability of the fair value of fixed-rate debt due to changes in the long-term benchmark interest rates. The hedged debt is marked to market, offsetting the effect of marking the interest rate swaps to market.
The carrying values and fair values of certain financial instruments as of March 31, 2014 and December 31, 2013 are shown in the following table. The carrying values of all other financial instruments approximate their estimated fair values. The counterparties to financial instruments consist of select major international financial institutions. Abbott does not expect any losses from nonperformance by these counterparties.
Carrying Value
Fair Value
Long-term Investment Securities:
24
Total Long-term Debt
(3,395
(3,918
(3,397
(3,930
Foreign Currency Forward Exchange Contracts:
Receivable position
49
(Payable) position
(56
(75
Interest Rate Hedge Contracts:
The fair value of the debt was determined based on significant other observable inputs, including current interest rates.
The following table summarizes the bases used to measure certain assets and liabilities at fair value on a recurring basis in the balance sheet:
Basis of Fair Value Measurement
Outstanding Balances
Quoted Prices in Active Markets
Significant Other Observable Inputs
Significant Unobservable Inputs
March 31, 2014:
Interest rate swap derivative financial instruments
Foreign currency forward exchange contracts
Total Assets
Fair value of hedged long-term debt
1,624
Contingent consideration related to business combinations
72
Total Liabilities
1,752
1,680
December 31, 2013:
197
1,623
208
1,906
1,698
The fair value of the debt was determined based on the face value of the debt adjusted for the fair value of the interest rate swaps, which is based on a discounted cash flow analysis. The fair value of foreign currency forward exchange contracts is determined using a market approach, which utilizes values for comparable derivative instruments. The fair value of the contingent consideration was determined based on an independent appraisal adjusted for the time value of money, exchange, payments and other changes in fair value. The change in contingent consideration from the previous year end primarily reflects the payment of contingent consideration in the first quarter of 2014.
12
Note 10 Litigation and Environmental Matters
Abbott has been identified as a potentially responsible party for investigation and cleanup costs at a number of locations in the United States and Puerto Rico under federal and state remediation laws and is investigating potential contamination at a number of company-owned locations. Abbott has recorded an estimated cleanup cost for each site for which management believes Abbott has a probable loss exposure. No individual site cleanup exposure is expected to exceed $4 million, and the aggregate cleanup exposure is not expected to exceed $15 million.
Abbott is involved in various claims and legal proceedings, and Abbott estimates the range of possible loss for its legal proceedings and environmental exposures to be from approximately $70 million to $90 million. The recorded accrual balance at March 31, 2014 for these proceedings and exposures was approximately $80 million. This accrual represents managements best estimate of probable loss, as defined by FASB ASC No. 450, Contingencies. Within the next year, legal proceedings may occur that may result in a change in the estimated loss accrued by Abbott. While it is not feasible to predict the outcome of all such proceedings and exposures with certainty, management believes that their ultimate disposition should not have a material adverse effect on Abbotts financial position, cash flows, or results of operations.
Note 11 Post-Employment Benefits
Retirement plans consist of defined benefit, defined contribution, and medical and dental plans. Net cost recognized in continuing operations for the three months ended March 31 for Abbotts major defined benefit plans and post-employment medical and dental benefit plans is as follows:
Defined Benefit Plans
Medical and Dental Plans
March 31, 2013
Service cost - benefits earned during the period
Interest cost on projected benefit obligations
77
Expected return on plans assets
(113
(93
(9
Net amortization of:
Actuarial loss, net
Prior service cost (credit)
(8
Net cost
Abbott funds its domestic defined benefit plans according to IRS funding limitations. International pension plans are funded according to similar regulations. In the first quarters of 2014 and 2013, $312 million and $208 million, respectively, were contributed to defined benefit plans and $40 million was contributed to the post-employment medical and dental benefit plans in each quarter.
Note 12 Taxes on Earnings
Taxes on earnings from continuing operations reflect the estimated annual effective rates and include charges for interest and penalties. In the first quarter of 2014, taxes on earnings from continuing operations reflect the recognition of $71 million of tax benefits as the result of the favorable resolution of various tax positions pertaining to prior years. Earnings from Discontinued Operations, net of tax, in the first quarter of 2014 reflects the recognition of $36 million of net tax benefits primarily as a result of the resolution of various tax positions related to AbbVies operations for years prior to the separation. The conclusion of these tax matters decreased the gross amount of unrecognized tax benefits by approximately $102 million. As a result of the American Taxpayer Relief Act of 2012 signed into law in January 2013, Abbott recorded a tax benefit to taxes on continuing operations of approximately $103 million in the first quarter of 2013 for the retroactive extension of the research tax credit and the look-through rules of section 954(c)(6) of the Internal Revenue Code to the beginning of 2012.
Tax authorities in various jurisdictions regularly review Abbotts income tax filings. Abbott believes that it is reasonably possible that the recorded amount of gross unrecognized tax benefits may decrease by up to $350 million, including cash adjustments, within the next twelve months as a result of concluding various domestic and international tax matters.
Note 13 Segment Information
Abbotts principal business is the discovery, development, manufacture and sale of a broad line of health care products. Abbotts products are generally sold directly to retailers, wholesalers, hospitals, health care facilities, laboratories, physicians offices and government agencies throughout the world. Abbotts reportable segments are as follows:
Established Pharmaceutical Products International sales of a broad line of branded generic pharmaceutical products.
Nutritional Products Worldwide sales of a broad line of adult and pediatric nutritional products.
Diagnostic Products Worldwide sales of diagnostic systems and tests for blood banks, hospitals, commercial laboratories and alternate-care testing sites. For segment reporting purposes, the Core Laboratories Diagnostics, Molecular Diagnostics, Point of Care and Ibis diagnostic divisions are aggregated and reported as the Diagnostic Products segment.
Vascular Products Worldwide sales of coronary, endovascular, structural heart, vessel closure and other medical device products.
Non-reportable segments include the Diabetes Care and Medical Optics segments.
Abbotts underlying accounting records are maintained on a legal entity basis for government and public reporting requirements. Segment disclosures are on a performance basis consistent with internal management reporting. Intersegment transfers of inventory are recorded at standard cost and are not a measure of segment operating earnings. The cost of some corporate functions and the cost of certain employee benefits are charged to segments at predetermined rates that approximate cost. Remaining costs, if any, are not allocated to segments. In addition, intangible asset amortization is not allocated to operating segments, and intangible assets and goodwill are not included in the measure of each segments assets. The following segment information has been prepared in accordance with the internal accounting policies of Abbott, as described above, and are not presented in accordance with generally accepted accounting principles applied to the consolidated financial statements.
Net Sales to External Customers
Operating Earnings
Established Pharmaceutical Products
1,151
1,233
230
286
Nutritional Products
1,631
1,699
283
342
Diagnostic Products
1,117
1,088
260
Vascular Products
738
742
221
188
Total Reportable Segments
4,637
4,762
956
1,076
607
616
Net Sales
Corporate functions and benefit plans costs
(58
(120
Non-reportable segments
63
88
Net interest expense
(23
(26
Share-based compensation (a)
(119
(126
(174
(199
Other, net (b)
(222
(139
(a) Approximately 40 to 45 percent of the annual net cost of share-based awards will typically be recognized in the first quarter due to the timing of the granting of share-based awards.
(b) The increase from 2013 to 2014 primarily reflects higher charges for cost reduction initiatives.
Financial Review - Results of Operations
The following table details sales by reportable segment for the three months ended March 31. Percent changes are versus the prior year and are based on unrounded numbers.
Total Change
Impact of Foreign Exchange
Total Change Excl. Foreign Exchange
(6.6
)%
(5.9
(0.7
(4.0
(2.3
(1.7
2.6
(2.5
5.1
(0.5
(1.5
1.0
(2.6
(3.1
0.5
(1.6
0.1
(3.0
Total U.S.
1,489
1,534
(2.9
Total International
3,755
3,844
(4.1
1.8
The net sales decline in 2014 reflects the impact of unfavorable changes in foreign currency exchange rates, partially offset by unit volume growth. The relatively stronger U.S. dollar decreased total international sales by 4.1 percent and total sales by 3.0 percent. Excluding the unfavorable impact of foreign exchange, total net sales increased 0.5 percent in 2014 due primarily to higher sales of diagnostic products, partially offset by lower nutritional product revenue. The strength in diagnostic products reflected continued momentum in core laboratory diagnostics, as well as higher international molecular sales particularly in emerging markets. The first quarter 2014 decline in nutritional products was due primarily to lower sales of pediatric products resulting from the impact of a previously reported supplier recall in August 2013 in certain international markets.
A comparison of significant product group sales for the three months ended March 31 is as follows. Percent changes are versus the prior year and are based on unrounded numbers.
Established Pharmaceutical Products sales
Key Emerging Markets
531
585
(9.2
(9.4
0.2
%
Developed and Other Markets
620
648
(4.2
(2.7
Nutritionals
U.S. Pediatric Nutritionals
365
385
(5.2
International Pediatric Nutritionals
608
(10.5
(2.8
(7.7
U.S. Adult Nutritionals
324
333
International Adult Nutritionals
398
373
6.6
(5.8
12.4
Diagnostics
Immunochemistry
856
832
2.9
5.7
Vascular Products (1)
Drug Eluting Stents (DES) and Bioresorbable Vascular Scaffold (BVS) products
368
(4.9
(2.4
Other Coronary products
146
(1.0
(0.8
(0.2
Endovascular
121
115
6.0
6.2
(1) Other Coronary Products include primarily guidewires and balloon catheters. Endovascular includes vessel closure, carotid stents and other peripheral products.
The Established Pharmaceutical Products segment is focused on 14 key emerging markets including India, Russia, China and Brazil. Sales in these key emerging markets declined 9% as strong growth in Brazil and India was offset by the negative impact of currencies as well as the timing of supply of key products in the segments womens health portfolio, primarily due to a planned plant shutdown to expand capacity. Sales in Developed and Other Markets in the Established Pharmaceutical Products segment decreased in 2014 due primarily to the unfavorable effects of exchange in 2014 and to price declines from the continued effect of European austerity measures. International Pediatric Nutritional sales decreased due primarily to the impact of a supplier recall in certain international markets in the third quarter of 2013, which created significant disruption in these markets that unfavorably impacted sales volumes. The decline in U.S Pediatric Nutritional revenue primarily reflects lower infant formula sales. In the Vascular Products segment, sales of DES products declined primarily as a result of sales declines in the U.S. due in part to the launch of a competitive drug-eluting stent. International sales of vascular products increased in the quarter driven by a number of new products and the increased penetration of Abbotts bioresorbable vascular scaffold.
The gross profit margin percentage was 49.6 percent for the first quarter 2014 compared to 51.1 percent for the first quarter 2013. The decline primarily reflects the impact of unfavorable foreign exchange in the diagnostics, established pharmaceuticals and nutritional businesses.
Research and development expenses increased by $41 million, or 11.6 percent, in the first quarter 2014 due primarily to the impact of restructuring actions recorded in the quarter. For the three months ended March 31, 2014, research and development expenditures totaled $77 million for the Vascular Products segment, $98 million for the Diagnostic Products segment, $50 million for the Established Pharmaceutical Products segment and $48 million for the Nutritional Products segment.
Selling, general and administrative expenses for the first quarter 2014 decreased 1.3 percent due in part to timing between quarters, as well as a continuing focus on cost savings initiatives.
Restructuring Plans
The results for the first three months of 2014 reflect charges recognized for actions associated with the companys plans to streamline various operations in order to reduce costs and improve efficiencies in Abbotts vascular, diagnostics, and nutritional businesses. Abbott recorded employee related severance and other charges of approximately $80 million in 2014 related to these initiatives. Approximately $17 million is recognized in Cost of products sold, $41 million is recognized in Research and development and approximately $22 million is recognized in Selling, general and administrative expense. In the first quarter of 2014, Abbott management also approved plans to streamline various operations in order to reduce costs and improve efficiencies across various functional areas and recognized a charge of $25 million. Approximately $2 million is recorded in Cost of products sold and approximately $23 million as Selling, general and administrative expense. See Note 7 to the financial statements, Restructuring Plans, for additional information regarding these charges.
Interest Expense (Income), net
Interest expense (income), net decreased $3 million in the first quarter 2014 compared to 2013 due to lower interest rates in the first quarter of 2014, which reduced total interest expense. Interest income was relatively unchanged from the prior year.
Taxes on Earnings from Continuing Operations
Taxes on earnings from continuing operations reflect the estimated annual effective rates and include charges for interest and penalties. In the first quarter of 2014, taxes on earnings from continuing operations reflect the recognition of $71 million of tax benefits as the result of the favorable resolution of various tax positions pertaining to prior years. Earnings from discontinued operations, net of tax, in the first quarter of 2014 reflects the recognition of $36 million of net tax benefits primarily as a result of the favorable resolution of various tax positions related to AbbVies operations for years prior to the separation. The conclusion of these tax matters decreased the gross amount of unrecognized tax benefits by approximately $102 million. As a result of the American Taxpayer Relief Act of 2012 signed into law in January 2013, Abbott recorded a tax benefit to taxes on continuing operations of approximately $103 million in the first quarter of 2013 for the retroactive extension of the research tax credit and the look-through rules of section 954(c)(6) of the Internal Revenue Code to the beginning of 2012. Excluding these discrete items, the change in the effective rate from 2013 to 2014 primarily reflects the impact of the repatriation of 2014 earnings generated outside the U.S.
Separation of AbbVie Inc.
Liquidity and Capital Resources March 31, 2014 Compared with December 31, 2013
The reduction of cash and cash equivalents from $3.5 billion at December 31, 2013 to $2.1 billion at March 31, 2014 reflects share repurchases and dividends paid in the quarter.
Net cash from operating activities for the first three months of 2014 totaled $336 million. Other, net in Net cash from operating activities for the first three months of 2014 of $(548) million reflects contributions to defined benefit plans of $312 million in 2014, as well as the non-cash impact in the first quarter of approximately $110 million of tax benefits from the resolution of various tax positions pertaining to prior years. The $(489) million of Other, net activity in Net cash from operating activities for 2013 reflects approximately $233 million of one-time net cash outflows related to the separation of AbbVie, the first quarter non-cash impact of the $103 million tax benefit for the retroactive impact of U.S. tax law changes due to the timing of tax filings and $208 million of contributions to defined benefit plans. Abbott expects annual cash flow from operating activities to continue to exceed Abbotts capital expenditures and cash dividends on an annual basis.
Working capital was $7.7 billion at March 31, 2014 and $9.7 billion at December 31, 2013. The $2.0 billion decrease in working capital in 2014 is due primarily to the use of cash to repurchase shares and pay a higher dividend.
A majority of Abbotts trade receivables in Italy, Spain, Portugal, and Greece are with governmental health systems. Governmental receivables in these four countries accounted for approximately 1% of Abbotts total assets and 9% of total net trade receivables as of March 31, 2014 as compared to 1% of total assets and 12% of total net receivables as of December 31, 2013. With the exception of Greece, Abbott historically has collected almost all of the outstanding receivables in these countries. Abbott closely monitors economic conditions and budgetary and other fiscal developments in these countries. Abbott regularly communicates with its customers regarding the status of receivable balances, including their payment plans and obtains positive confirmation of the validity of the receivables. Abbott also monitors the potential for and periodically has utilized factoring arrangements to mitigate risk although such arrangements were not material in the first three months of 2014.
At March 31, 2014 Abbotts long-term debt rating was A+ by Standard & Poors Corporation and A1 by Moodys Investors Service. Abbott has readily available financial resources, including unused lines of credit of $5.0 billion that support commercial paper borrowing arrangements which expire in 2017.
In June 2013, the board of directors authorized the purchase of up to $3.0 billion of Abbotts common shares from time to time and 54.6 million shares at a cost of $2.1 billion were purchased in the first three months of 2014. Approximately $512 million remains available for repurchase under this authorization. In the first three months of 2013, 25.0 million shares were purchased at a cost of $850 million under a previous share repurchase authorization.
In the first quarter of 2014, Abbott declared a dividend of $0.22 per share on its common shares, which represents a 57% increase over the $0.14 per share dividend declared in the first quarter of 2013.
Legislative Issues
Abbotts primary markets are highly competitive and subject to substantial government regulations throughout the world. Abbott expects debate to continue over the availability, method of delivery, and payment for health care products and services. It is not possible to predict the extent to which Abbott or the health care industry in general might be adversely affected by these factors in the future. A more complete discussion of these factors is contained in Item 1, Business, and Item 1A, Risk Factors, in the 2013 Annual Report on Form 10-K.
Private Securities Litigation Reform Act of 1995 A Caution Concerning Forward-Looking Statements
Under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, Abbott cautions investors that any forward-looking statements or projections made by Abbott, including those made in this document, are subject to risks and uncertainties that may cause actual results to differ materially from those projected. Economic, competitive, governmental, technological and other factors that may affect Abbotts operations are discussed in Item 1A, Risk Factors, in the 2013 Annual Report on Form 10-K.
PART I. FINANCIAL INFORMATION
(a) Evaluation of disclosure controls and procedures. The Chief Executive Officer, Miles D. White, and Chief Financial Officer, Thomas C. Freyman, evaluated the effectiveness of Abbott Laboratories disclosure controls and procedures as of the end of the period covered by this report, and concluded that Abbott Laboratories disclosure controls and procedures were effective to ensure that information Abbott is required to disclose in the reports that it files or submits with the Securities and Exchange Commission (the Commission) under the Securities Exchange Act of 1934 (the Exchange Act) is recorded, processed, summarized and reported, within the time periods specified in the Commissions rules and forms, and to ensure that information required to be disclosed by Abbott in the reports that it files or submits under the Exchange Act is accumulated and communicated to Abbotts management, including its principal executive officer and principal financial officer, as appropriate to allow timely decisions regarding required disclosure.
(b) Changes in internal control over financial reporting. During the quarter ended March 31, 2014, there were no changes in Abbotts internal control over financial reporting (as defined in Rule 13a-15(f) under the Exchange Act) that have materially affected, or are reasonably likely to materially affect, Abbotts internal control over financial reporting.
PART II. OTHER INFORMATION
Abbott is involved in various claims, legal proceedings and investigations, including (as of March 31, 2014, except where noted below) those described below. While it is not feasible to predict the outcome of such pending claims, proceedings and investigations with certainty, management is of the opinion that their ultimate resolution should not have a material adverse effect on Abbotts financial position, cash flows, or results of operations.
In its 2013 Annual Report on Form 10-K, Abbott reported that Medinol Limited (Medinol) sued Abbott in the Netherlands asserting that certain of Abbotts coronary bare metal and all of its metal-based drug eluting stent products infringe certain of Medinols European stent design patents, and that in January 2013, Medinol appealed the lower courts findings of noninfringement to the Dutch Supreme Court. In April 2014, the Dutch Supreme Court rejected Medinols appeal, resulting in a final determination that Abbotts stents do not infringe Medinols patents.
(c) Issuer Purchases of Equity Securities
Period
(a) Total Number of Shares (or Units) Purchased
(b) Average Price Paid per Share (or Unit)
(c) Total Number of Shares (or Units) Purchased as Part of Publicly Announced Plans or Programs
(d) Maximum Number (or Approximate Dollar Value) of Shares (or Units) that May Yet Be Purchased Under the Plans or Programs
January 1, 2014 January 31, 2014
6,629,302
(1)
36.462
6,500,000
2,374,933,131
(2)
February 1, 2014 February 28, 2014
25,746,238
38.211
25,700,000
1,392,882,137
March 1, 2014 March 31, 2014
22,407,140
39.415
22,360,000
511,537,561
54,782,680
38.492
54,560,000
(1) These shares include:
(i) the shares deemed surrendered to Abbott to pay the exercise price in connection with the exercise of employee stock options 129,302 in January, 46,238 in February, and 16,640 in March; and
(ii) the shares purchased on the open market for the benefit of participants in the Abbott Laboratories, Limited Employee Stock Purchase Plan - 0 in January, 0 in February, and 30,500 in March.
These shares do not include the shares surrendered to Abbott to satisfy tax withholding obligations in connection with the vesting of restricted stock or restricted stock units.
(2) On June 14, 2013, Abbott announced that its board of directors approved the purchase of up to $3 billion of its common shares, from time to time.
Incorporated by reference to the Exhibit Index included herewith.
SIGNATURE
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
By:
/s/ Thomas C. Freyman
Thomas C. Freyman
Executive Vice President,
Finance and Chief Financial Officer
Date: May 7, 2014
EXHIBIT INDEX
Exhibit No.
Exhibit
10.1
Abbott Laboratories 2009 Incentive Stock Program, as amended and restated.
Statement re: Computation of Ratio of Earnings to Fixed Charges.
31.1
Certification of Chief Executive Officer Required by Rule 13a-14(a) (17 CFR 240.13a-14(a)).
31.2
Certification of Chief Financial Officer Required by Rule 13a-14(a) (17 CFR 240.13a-14(a)).
Exhibits 32.1 and 32.2 are furnished herewith and should not be deemed to be filed under the Securities Exchange Act of 1934.
32.1
Certification of Chief Executive Officer Pursuant to 18 U.S.C. Section 1350, as Adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
32.2
Certification of Chief Financial Officer Pursuant to 18 U.S.C. Section 1350, as Adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
101
The following financial statements and notes from the Abbott Laboratories Quarterly Report on Form 10-Q for the quarter ended March 31, 2014, formatted in XBRL: (i) Condensed Consolidated Statement of Earnings; (ii) Condensed Consolidated Statement of Comprehensive Income; (iii) Condensed Consolidated Balance Sheet; (iv) Condensed Consolidated Statement of Cash Flows; and (v) the notes to the condensed consolidated financial statements.
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