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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 10-Q
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15 (d)
OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended Commission file number 1-1225
June 30, 2001
AMERICAN HOME PRODUCTS CORPORATION
----------------------------------
(Exact name of registrant as specified in its charter)
Delaware 13-2526821
-------- ----------
(State or other jurisdiction of (I.R.S. Employer Identification No.)
incorporation or organization)
Five Giralda Farms, Madison, N.J. 07940
--------------------------------- -----
(Address of principal executive offices) (Zip Code)
Registrant's telephone number, including area code (973) 660-5000
Indicate by check mark whether the registrant (1) has filed all
reports required to be filed by Section 13 or 15 (d)
of the Securities Exchange Act of 1934 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
------ --
The number of shares of Common Stock outstanding as of the close of business on
July 31, 2001:
Number of
Class Shares Outstanding
--------------------------------- ------------------
Common Stock, $0.33-1/3 par value 1,317,594,283
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AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
INDEX
Page No.
--------
Part I - Financial Information 2
Item 1. Consolidated Condensed Financial Statements:
Consolidated Condensed Balance Sheets -
June 30, 2001 and December 31, 2000 3
Consolidated Condensed Statements of Operations -
Three and Six Months Ended June 30, 2001 and 2000 4
Consolidated Condensed Statements of Changes in
Stockholders' Equity - Six Months Ended June 30,
2001 and 2000 5
Consolidated Condensed Statements of Cash Flows -
Six Months Ended June 30, 2001 and 2000 6
Notes to Consolidated Condensed Financial Statements 7-13
Item 2. Management's Discussion and Analysis of
Financial Condition and Results of Operations 14-23
Part II - Other Information 24
Item 1. Legal Proceedings 24-25
Item 4. Submission of Matters to a Vote of Security-Holders 26
Item 6. Exhibits and Reports on Form 8-K 27
Signature 28
Exhibit Index EX-1
Items other than those listed above have been omitted because they are not
applicable.
1
Part I - Financial Information
------------------------------
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
The consolidated condensed financial statements included herein have been
prepared by American Home Products Corporation (the "Company"), without audit,
pursuant to the rules and regulations of the Securities and Exchange Commission.
Certain information and footnote disclosures normally included in financial
statements prepared in accordance with accounting principles generally accepted
in the United States have been condensed or omitted pursuant to such rules and
regulations; however, the Company believes that the disclosures are adequate to
make the information presented not misleading. In the opinion of management, the
consolidated condensed financial statements include all adjustments necessary to
present fairly the financial position of the Company as of June 30, 2001 and
December 31, 2000, and the results of its operations, changes in stockholders'
equity and cash flows for the three months and six months ended June 30, 2001
and 2000. It is suggested that these consolidated condensed financial statements
and management's discussion and analysis of financial condition and results of
operations be read in conjunction with the financial statements and the notes
thereto included in the Company's 2000 Annual Report on Form 10-K and Quarterly
Report on Form 10-Q for the quarter ended March 31, 2001.
In the 2000 fourth quarter, the Company sold a portion of its ownership in
Immunex Corporation (Immunex) common stock, which reduced the Company's
ownership interest below 50%. As a result, the financial results of Immunex,
which previously were consolidated in the financial results of the Company, were
deconsolidated and included in the financial results of the Company on an equity
basis retroactive to January 1, 2000. Accordingly, alliance revenue relating to
co-promotion agreements between the Company and Immunex was included in
pharmaceutical net revenue for both the 2001 and 2000 second quarters and first
halves. The 2000 second quarter and first half financial results were restated
to reflect the deconsolidation of Immunex, which had no effect on income from
continuing operations.
As of January 1, 2001, the Company early adopted new authoritative accounting
guidance reflecting certain rebates and sales incentives (i.e., coupons and
other rebate programs) as reductions of revenues instead of selling and
marketing expenses. Financial information for all prior periods presented has
been reclassified to comply with the income statement classification
requirements of the new guidance.
2
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
CONSOLIDATED CONDENSED BALANCE SHEETS
(In Thousands Except Per Share Amounts)
June 30, December 31,
2001 2000
----------- ------------
ASSETS
Cash and cash equivalents $2,393,349 $2,644,306
Marketable securities 755,880 341,031
Accounts receivable less allowances 2,388,758 2,740,272
Inventories:
Finished goods 650,611 585,123
Work in progress 661,699 586,656
Materials and supplies 397,996 359,948
----------- ------------
1,710,306 1,531,727
Other current assets including deferred taxes 2,607,754 2,923,475
----------- ------------
Total Current Assets 9,856,047 10,180,811
Property, plant and equipment 7,995,138 7,578,233
Less accumulated depreciation 2,581,014 2,543,409
----------- ------------
5,414,124 5,034,824
Goodwill and other intangibles, net of accumulated
amortization 3,942,136 4,052,410
Other assets including deferred taxes 2,165,998 1,824,421
----------- ------------
Total Assets $21,378,305 $21,092,466
=========== ============
LIABILITIES
Loans payable $52,165 $58,717
Trade accounts payable 874,503 595,233
Accrued expenses 4,651,135 8,831,459
Accrued federal and foreign taxes 244,075 256,650
----------- ------------
Total Current Liabilities 5,821,878 9,742,059
Long-term debt 8,023,186 2,394,790
Other noncurrent liabilities 3,483,461 5,226,495
Accrued postretirement benefit obligations other than pensions 927,365 911,029
STOCKHOLDERS' EQUITY
$2.00 convertible preferred stock, par value $2.50 per share 53 55
Common stock, par value $0.33-1/3 per share 438,908 437,258
Additional paid-in capital 4,092,308 3,952,457
Accumulated deficit (598,579) (899,118)
Accumulated other comprehensive loss (810,275) (672,559)
----------- ------------
Total Stockholders' Equity 3,122,415 2,818,093
----------- ------------
Total Liabilities and Stockholders' Equity $21,378,305 $21,092,466
=========== ============
The accompanying notes are an integral part of these consolidated condensed financial statements.
3
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
CONSOLIDATED CONDENSED STATEMENTS OF OPERATIONS
(In Thousands Except Per Share Amounts)
Three Months Six Months
Ended June 30, Ended June 30,
-------------------------- --------------------------
2001 2000 2001 2000
---------- ---------- ---------- ----------
Net Revenue $3,216,420 $3,026,215 $6,665,596 $6,222,067
---------- ---------- ---------- ----------
Cost of goods sold 791,041 771,042 1,589,644 1,553,034
Selling, general and administrative expenses 1,291,455 1,242,953 2,576,923 2,407,157
Research and development expenses 477,533 412,773 928,522 820,991
Interest expense, net 49,554 51,990 53,493 102,874
Other income, net (25,053) (7,063) (95,864) (73,463)
Termination fee - - - (1,709,380)
---------- ---------- ---------- ----------
Income from continuing operations before
federal and foreign taxes 631,890 554,520 1,612,878 3,120,854
Provision for federal and foreign taxes 154,894 141,786 402,328 962,111
---------- ---------- ---------- ----------
Income from continuing operations 476,996 412,734 1,210,550 2,158,743
---------- ---------- ---------- ----------
Discontinued Operations:
Income from operations of agricultural products
business (net of federal and foreign taxes of $57,289) - - - 103,346
Loss on disposal of agricultural products business
(including federal and foreign tax charges of $855,248) - - - (1,572,993)
---------- ---------- ---------- ----------
Loss from discontinued operations - - - (1,469,647)
---------- ---------- ---------- ----------
Net Income $476,996 $412,734 $1,210,550 $689,096
========== ========== ========== ==========
Basic earnings per share from continuing operations $0.36 $0.32 $0.92 $1.66
Basic loss per share from discontinued operations - - - (1.13)
---------- ---------- ---------- ----------
Basic earnings per share $0.36 $0.32 $0.92 $0.53
========== ========== ========== ==========
Diluted earnings per share from continuing operations $0.36 $0.31 $0.91 $1.63
Diluted loss per share from discontinued operations - - - (1.11)
---------- ---------- ---------- ----------
Diluted earnings per share $0.36 $0.31 $0.91 $0.52
========== ========== ========== ==========
Dividends per share of common stock $0.23 $0.23 $0.46 $0.46
========== ========== ========== ==========
The accompanying notes are an integral part of these consolidated condensed financial statements.
4
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
CONSOLIDATED CONDENSED STATEMENTS OF CHANGES IN STOCKHOLDERS' EQUITY
(In Thousands Except Per Share Amounts)
Six Months Ended June 30, 2001:
$2.00 Accumulated
Convertible Additional Other Total
Preferred Common Paid-in Accumulated Comprehensive Stockholders'
Stock Stock Capital Deficit Loss Equity
----------- --------- ----------- ----------- ------------- -------------
Balance at January 1, 2001 $55 $437,258 $3,952,457 ($899,118) ($672,559) $2,818,093
Net income 1,210,550 1,210,550
Currency translation adjustments (155,729) (155,729)
Unrealized gain on derivative
contracts 16,135 16,135
Unrealized gain on marketable
securities 1,878 1,878
------------
Comprehensive income 1,072,834
------------
Cash dividends declared * (907,287) (907,287)
Common stock issued for stock options 1,548 127,337 128,885
Conversion of preferred stock
and other exchanges (2) 102 12,514 (2,724) 9,890
---------- -------- ---------- ---------- ------------- ------------
Balance at June 30, 2001 $53 $438,908 $4,092,308 ($598,579) ($810,275) $3,122,415
========== ======== ========== ========== ============= ============
Six Months Ended June 30, 2000:
$2.00 Accumulated
Convertible Additional Other Total
Preferred Common Paid-in Retained Comprehensive Stockholders'
Stock Stock Capital Earnings Loss Equity
----------- --------- ----------- ----------- ------------- -------------
Balance at January 1, 2000 $61 $434,639 $3,392,705 $3,000,827 ($613,485) $6,214,747
Net income 689,096 689,096
Currency translation adjustments (490) (490)
Unrealized gain on marketable
securities 15,380 15,380
------------
Comprehensive income 703,986
------------
Cash dividends declared (599,949) (599,949)
Common stock acquired for treasury (2,261) (14,884) (341,901) (359,046)
Common stock issued for stock options 1,948 144,880 146,828
Conversion of preferred stock
and other exchanges (4) 104 21,164 (3,697) 17,567
---------- -------- ---------- ---------- ------------ ------------
Balance at June 30, 2000 $57 $434,430 $3,543,865 $2,744,376 ($598,595) $6,124,133
========== ======== ========== ========== ============ ============
* Includes the 2001 third quarter common stock cash dividend of $0.23 per share ($302,847 in the aggregate) declared on
June 21, 2001 and payable on September 1, 2001, and the 2001 second and third quarter preferred stock cash dividends
of $0.50 per share ($21 in the aggregate) paid on July 1, 2001 and payable on October 1, 2001, respectively.
The accompanying notes are an integral part of these consolidated condensed financial statements.
5
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
CONSOLIDATED CONDENSED STATEMENTS OF CASH FLOWS
(In Thousands)
Six Months
Ended June 30,
-------------------------
2001 2000
---------- ----------
Operating Activities
- --------------------
Income from continuing operations $1,210,550 $2,158,743
Adjustments to reconcile income from continuing operations to net cash
provided from (used for) operating activities of continuing operations:
Gains on sales of assets (102,577) (78,093)
Depreciation and amortization 294,924 270,507
Deferred income taxes 163,360 355,784
Changes in working capital, net 55,314 492,247
Diet drug litigation payments (5,948,929) (1,273,927)
Deconsolidation of Immunex - (236,768)
Other items, net (52,058) (156,430)
---------- ----------
Net cash provided from (used for) continuing operations (4,379,416) 1,532,063
Net cash provided from discontinued operations - 127,574
---------- ----------
Net cash provided from (used for) operating activities (4,379,416) 1,659,637
---------- ----------
Investing Activities
- --------------------
Purchases of property, plant and equipment (843,225) (553,716)
Proceeds from sale of the agricultural products business - 3,800,000
Proceeds from sales of assets 253,350 99,321
Proceeds from sales and maturities of marketable securities 114,298 187,300
Purchases of marketable securities (529,147) (375,490)
---------- ----------
Net cash provided from (used for) investing activities (1,004,724) 3,157,415
---------- ----------
Financing Activities
- --------------------
Net proceeds from (repayments of) debt 5,626,438 (3,110,414)
Dividends paid (604,419) (599,949)
Exercises of stock options 128,885 146,828
Purchases of common stock for treasury - (359,046)
---------- ----------
Net cash provided from (used for) financing activities 5,150,904 (3,922,581)
---------- ----------
Effects of exchange rates on cash balances (17,721) (18,440)
---------- ----------
Increase (decrease) in cash and cash equivalents (250,957) 876,031
Cash and cash equivalents, beginning of period 2,644,306 1,892,715
---------- ----------
Cash and cash equivalents, end of period $2,393,349 $2,768,746
========== ==========
Supplemental Information
- ------------------------
Interest payments $120,469 $235,751
Income tax payments, net of refunds 241,287 343,792
The accompanying notes are an integral part of these consolidated condensed financial statements.
6
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
NOTES TO CONSOLIDATED CONDENSED FINANCIAL STATEMENTS
Note 1. Credit Facilities and Term Debt Financing
-----------------------------------------
In addition to the Company's existing $2,000.0 million credit
facility, in March 2001, the Company obtained new credit facilities
totaling $6,000.0 million. The new credit facilities include a
$3,000.0 million, 364-day credit facility (which support borrowings
under the commercial paper program). Any borrowings actually drawn
from the credit facility are extendible for an additional year. The
portion of commercial paper outstanding at June 30, 2001 supported by
the $3,000.0 million credit facility was classified as long-term debt
since the Company intends, and has the ability, to refinance these
obligations through the issuance of additional commercial paper or
through the use of its $3,000.0 million credit facility as described
above. The credit facility contains substantially identical financial
and other covenants, representations, warranties, conditions and
default provisions as the Company's existing $2,000.0 million credit
facility, which terminates on July 31, 2002.
In addition, the new credit facilities included a $3,000.0 million,
364-day bridge facility, which facility was terminated when the
Company issued $3,000.0 million of Senior Notes (the "Notes") on March
30, 2001. On March 30, 2001, the Company issued three tranches of
Notes in a transaction exempt from registration under the Securities
Act of 1933, as amended (the "Securities Act"), pursuant to Rule 144A,
as follows:
o $500.0 million 5.875% Notes due March 15, 2004
o $1,000.0 million 6.25% Notes due March 15, 2006
o $1,500.0 million 6.70% Notes due March 15, 2011
In connection with the Notes, the Company filed a Registration
Statement on Form S-4 with the Securities and Exchange Commission
(SEC) on April 27, 2001 in order to offer the holders of the Notes the
ability to exchange the outstanding Notes for new notes with
substantially identical terms, but which are registered under the
Securities Act. The Company's Registration Statement was declared
effective by the SEC on May 8, 2001. As of June 15, 2001, the date the
offer to exchange the Notes concluded, substantially all the Notes had
been exchanged for the new notes registered under the Securities Act.
Interest on the Notes is payable semi-annually, on March 15 and
September 15, and is subject to adjustment under certain
circumstances. The Company entered into two $750.0 million notional
amount interest rate swaps relating to the $1,500.0 million 6.70%
Notes. The interest rate swaps are contracts under which the Company
converted the fixed rate on the $1,500.0 million 6.70% Notes to a
floating rate of interest (the LIBOR swap rate) over the term of the
swap agreements, which is the same term as the underlying debt. The
interest rate swaps function as fair value hedges of the risk of
changes in the fair value of the Notes attributable to changes in the
benchmark interest rate (the LIBOR swap rate).
Any proceeds from commercial paper supported by the credit facilities
and the proceeds from the issuance of the Notes are being used for the
Company's general corporate and working capital requirements,
including payments related to the REDUX and PONDIMIN diet drug
litigation.
7
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
NOTES TO CONSOLIDATED CONDENSED FINANCIAL STATEMENTS
Note 2. Discontinued Operations
-----------------------
On March 20, 2000, the Company signed a definitive agreement with BASF
Aktiengesellschaft (BASF) to sell the agricultural products business
which manufactures, distributes and sells crop protection and pest
control products worldwide. On June 30, 2000, the sale was completed
and BASF paid the Company $3,800.0 million in cash and assumed certain
debt. As a result, the Company recorded an after-tax loss on the sale
of this business of $1,573.0 million or $1.19 per share-diluted and
reflected this business as a discontinued operation in the 2000 first
quarter.
Note 3. Contingencies and Litigation Settlement
---------------------------------------
The Company is involved in various legal proceedings, including
product liability and environmental matters of a nature considered
normal to its business. It is the Company's policy to accrue for
amounts related to these legal matters if it is probable that a
liability has been incurred and an amount is reasonably estimable.
In the 2000 fourth quarter, the Company recorded a $7,500.0 million
litigation charge for the estimated final amount required to resolve
all REDUX and PONDIMIN diet drug litigation, including all anticipated
payments in connection with the nationwide, class action settlement,
payments to the opt out claimants with whom the Company has agreed to
settle, and all anticipated payments to resolve the claims of the
remaining opt outs and any primary pulmonary hypertension (PPH)
claimants, as well as all legal fees and other costs. The Company
recorded an initial litigation charge of $4,750.0 million, net of
insurance, related to the diet drug litigation in the 1999 third
quarter.
During the 2001 first half, payments to the nationwide, class action
settlement funds, individual settlement payments, legal fees and other
costs totaling $5,948.9 million were paid and applied against the
litigation accrual. As of June 30, 2001, $2,216.6 million of the
litigation accrual remained.
In the opinion of the Company, although the outcome of any legal
proceedings cannot be predicted with certainty, the ultimate liability
of the Company in connection with its legal proceedings will not have
a material adverse effect on the Company's financial position but
could be material to the results of operations or cash flows in any
one accounting period.
Note 4. Restructuring Programs
----------------------
In December 1998, the Company recorded a special charge for
restructuring and related asset impairments of $321.2 million to
recognize costs of the reorganization of its worldwide supply chains
and U.S. distribution systems, and the globalization of certain
business units. The restructuring will ultimately result in the
8
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
NOTES TO CONSOLIDATED CONDENSED FINANCIAL STATEMENTS
elimination of approximately 3,900 positions worldwide offset, in
part, by 1,000 newly created positions in the same functions at other
locations. At June 30, 2001, approximately 3,670 positions had been
eliminated, and two distribution centers owned by the Company and a
leased distribution center had been closed. The Company anticipates
closing a total of 14 manufacturing plants; eight were closed in 2000
and two were closed during the first six months of 2001. The Company
currently anticipates closing another plant by the end of 2001, and
the remaining facilities in 2002, assuming no further delays in
regulatory approvals.
The activity in the restructuring accruals was as follows:
Personnel Other Closure/
(In thousands) Costs Exit Costs Total
------------------------------------------- --------- -------------- --------
Restructuring accruals at December 31, 2000 $6,249 $59,635 $65,884
Cash expenditures (8,063) (8,672) (16,735)
Redistributions 14,000 (14,000) --
------- ------- -------
Restructuring accruals at June 30, 2001 $12,186 $36,963 $49,149
======= ======= =======
During the 2001 second quarter, the Company made redistribution
adjustments between categories to increase accrual balances for
personnel costs by $14.0 million and decrease other closure/exit costs
by $14.0 million. These redistributions were necessary due to higher
than expected enhanced pension benefits and outplacement costs for
non-U.S. employees, updated forecasts of employees within the affected
facilities, and lower than expected other closure and exit costs.
The original scope of the restructuring projects remains substantially
unchanged.
Note 5. Derivative Instruments and Foreign Currency Risk Management Programs
--------------------------------------------------------------------
As of January 1, 2001, the Company adopted Statement of Financial
Accounting Standards (SFAS) Nos. 133 and 138, which require that all
derivative financial instruments be measured at fair value and be
recognized as assets or liabilities on the balance sheet with changes
in the fair value of the derivatives recognized in either net income
(loss) or accumulated other comprehensive income (loss), depending on
the designated purpose of the derivative. The impact on the Company's
financial results, upon the adoption of these pronouncements, was
immaterial.
On the date that the Company enters into a derivative contract, it
designates the derivative as: (1) a hedge of the fair value of a
recognized asset or liability (fair value hedge), (2) a hedge of a
forecasted transaction or the variability of cash flows that are to be
received or paid in connection with a recognized asset or liability
9
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
NOTES TO CONSOLIDATED CONDENSED FINANCIAL STATEMENTS
(cash flow hedge), (3) a foreign currency fair value or cash flow
hedge (foreign currency hedge) or (4) an instrument that is not
designated for hedge accounting treatment. For derivative contracts
that are designated and qualify as fair value hedges (including
foreign currency fair value hedges), the derivative instrument is
marked-to-market with gains and losses recognized in current period
earnings to offset the respective losses and gains recognized on the
underlying exposure. For derivative contracts that are designated and
qualify as cash flow hedges (including foreign currency cash flow
hedges), the effective portion of gains and losses on these contracts
are reported as a component of accumulated other comprehensive income
(loss) and reclassified into earnings in the same period the hedged
transaction affects earnings. Any hedge ineffectiveness on cash flow
hedges is immediately recognized in earnings. In certain circumstances
the Company enters into derivative contracts that are not designated
as hedging instruments. These derivative contracts are recorded at
fair value with the gain or loss recognized in current period
earnings. The Company does not hold any derivative instruments for
trading purposes.
The Company currently engages in two primary programs to manage its
exposure to foreign currency risk, as well as interest rate swaps to
manage its exposure to interest rate fluctuations. The derivative
contracts outstanding as of June 30, 2001 are as follows:
1. Short-term foreign exchange forward contracts to manage
foreign currency balance sheet exposures. These contracts do
not have a hedging designation and are recorded at fair
value with any gains or losses recognized in current period
earnings. For the six months ended June 30, 2001, the
Company recorded $24.7 million in Other income, net relating
to gains on these foreign exchange forward contracts. The
$24.7 million consists of gains from contracts settled
during the 2001 first half, as well as contracts outstanding
at June 30, 2001 that are marked to fair value.
2. Cash flow hedging program to cover currency risk related to
intercompany inventory sales denominated in foreign
currencies through the purchase of primarily foreign
currency put options. As of June 30, 2001, $16.1 million of
gains relating to the cash flow hedging program was included
in Accumulated other comprehensive loss. The Company also
purchases foreign currency put options outside of the cash
flow hedging program to protect additional intercompany
inventory sales. These put options do not have a hedging
designation and are recorded at fair value with all gains or
losses recognized in current period earnings. For the six
months ended June 30, 2001, the company has recorded gains
of $4.8 million in Other income, net relating to these
foreign currency put options.
3. Fair value interest rate swaps to manage interest rate
exposures. The Company strives to achieve an acceptable
balance between fixed- and floating-rate debt and investment
positions and has entered into effective fair value interest
rate swaps to maintain that balance. The fair value interest
rate swaps converted a portion of the Company's fixed-rate
debt into floating-rate debt. The fair value of the
Company's two $750.0 million notional amount interest rate
swaps relating to the $1,500.0 million 6.70% Notes, as of
June 30, 2001, is $40.7 million. The $40.7 million has been
recorded in Other noncurrent liabilities, offset by the
change in the fair value of the $1,500.0 million 6.70% Notes
of $40.7 million included in Long-term debt.
Refer to the "Quantitative and Qualitative Disclosures about Market
Risk" section on pages 21 and 22 for further discussion and
disclosures relating to the Company's derivative instruments and
foreign currency risk management programs.
10
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
NOTES TO CONSOLIDATED CONDENSED FINANCIAL STATEMENTS
Note 6. Company Data by Operating Segment
---------------------------------
The Company has three reportable segments: Pharmaceuticals, Consumer
Health Care and Corporate. The Company's Pharmaceuticals and Consumer
Health Care reportable segments are strategic business units that are
managed separately because they manufacture, distribute, and sell
distinct products and provide services which require various
technologies and marketing strategies.
Net Revenue (1)
-----------------------------------------
Three Months Six Months
Ended June 30, Ended June 30,
($ in millions) ------------------- -------------------
Operating Segment 2001 2000 2001 2000
-------------------- -------- -------- -------- --------
Pharmaceuticals (2) $2,694.0 $2,523.3 $5,573.3 $5,126.3
Consumer Health Care 522.4 502.9 1,092.3 1,095.8
-------- -------- -------- --------
Total $3,216.4 $3,026.2 $6,665.6 $6,222.1
======== ======== ======== ========
Income from Continuing Operations
Before Taxes (3)
-----------------------------------------
Three Months Six Months
Ended June 30, Ended June 30,
($ in millions) ------------------- -------------------
Operating Segment 2001 2000 2001 2000
--------------------- -------- -------- -------- --------
Pharmaceuticals $601.2 $549.0 $1,516.7 $1,293.0
Consumer Health Care 112.1 96.9 236.1 227.4
-------- -------- -------- --------
713.3 645.9 1,752.8 1,520.4
Corporate (4) (81.4) (91.4) (139.9) 1,600.5
-------- -------- -------- --------
Total $631.9 $554.5 $1,612.9 $3,120.9
======== ======== ======== ========
(1) The Company early adopted new authoritative accounting guidance
as of January 1, 2001 reflecting certain rebates and sales
incentives (i.e., coupons and other rebate programs) as
reductions of revenues instead of selling and marketing expenses.
Financial information for all prior periods presented has been
reclassified to comply with the income statement classification
requirements of the new guidance. These reclassifications had no
effect on total net revenue growth between the periods presented.
(2) Effective January 1, 2000, the financial results of Immunex,
which previously were consolidated in the results of the Company,
were deconsolidated and included in the financial results of the
Company on an equity basis. As a result, alliance revenue
relating to co-promotion agreements between the Company and
Immunex is included in pharmaceutical net revenue for both 2001
and 2000. The 2000 second quarter and first half pharmaceutical
net revenue was restated to reflect the deconsolidation.
(3) The second quarter results included goodwill amortization for
2001 and 2000 as follows: Pharmaceuticals - $34.1 and $36.7, and
Consumer Health Care - $5.9 and $8.0, respectively.
The first half results included goodwill amortization for 2001
and 2000 as follows: Pharmaceuticals - $68.7 and $75.6, Consumer
Health Care - $11.9 and $16.0, respectively.
(4) Corporate expenses for the 2000 first half included income of
$1,709.4 resulting from the receipt of a $1,800.0 termination fee
provided for under the merger agreement with Warner-Lambert
Company offset, in part, by certain related expenses.
11
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
NOTES TO CONSOLIDATED CONDENSED FINANCIAL STATEMENTS
Note 7. Earnings per Share
------------------
The following table sets forth the computations of basic earnings per
share and diluted earnings per share:
Three Months Six Months
Ended June 30, Ended June 30,
----------------------- ------------------------
(In thousands except per share amounts) 2001 2000 2001 2000
---------------------------------------------------------- --------- --------- ---------- ----------
Income from continuing operations less preferred dividends $476,975 $412,723 $1,210,518 $2,158,720
Loss from discontinued operations - - - (1,469,647)
--------- --------- ---------- ----------
Net income less preferred dividends $476,975 $412,723 $1,210,518 $689,073
Denominator:
Average number of common shares outstanding 1,316,008 1,304,049 1,314,938 1,304,631
--------- --------- ---------- ----------
Basic earnings per share from continuing operations $0.36 $0.32 $0.92 $1.66
Basic loss per share from discontinued operations - - - (1.13)
--------- --------- ---------- ----------
Basic earnings per share $0.36 $0.32 $0.92 $0.53
========= ========= ========== ==========
Income from continuing operations $476,996 $412,734 $1,210,550 $2,158,743
Loss from discontinued operations - - - (1,469,647)
--------- --------- ---------- ----------
Net income $476,996 $412,734 $1,210,550 $689,096
Denominator:
Average number of common shares outstanding 1,316,008 1,304,049 1,314,938 1,304,631
Common share equivalents of outstanding stock
options and deferred contingent common stock awards 14,649 17,375 14,423 15,917
--------- --------- ---------- ----------
Total shares 1,330,657 1,321,424 1,329,361 1,320,548
--------- --------- ---------- ----------
Diluted earnings per share from continuing operations $0.36 $0.31 $0.91 $1.63
Diluted loss per share from discontinued operations - - - (1.11)
--------- --------- ---------- ----------
Diluted earnings per share $0.36 $0.31 $0.91 $0.52
========= ========= ========== ==========
Note 8. Accumulated Other Comprehensive Loss
------------------------------------
Accumulated other comprehensive loss consists of changes in foreign
currency translation adjustments, unrealized gains on derivative
contracts, and unrealized gains on marketable securities. The
following table sets forth the changes in each component and the
applicable tax effect, if any. Reclassification adjustments represent
items that are included in net income in the current period but
previously were reported in Accumulated other comprehensive loss.
12
AMERICAN HOME PRODUCTS CORPORATION AND SUBSIDIARIES
NOTES TO CONSOLIDATED CONDENSED FINANCIAL STATEMENTS
Six Months Ended June 30, 2001
----------------------------------
(In thousands) Pre-tax Tax After Tax
---------------------------------------------------- --------- ------ ---------
Foreign currency translation adjustments ($155,729) - ($155,729)
--------- ------ ---------
Unrealized gains on derivative contracts:
Unrealized holding gains arising during the period 32,556 11,804 20,752
Less: reclassification adjustments for gains
realized in net income 7,103 2,486 4,617
--------- ------ ---------
Net unrealized gains on derivative contracts 25,453 9,318 16,135
Unrealized gains on marketable securities 1,878 - 1,878
--------- ------ ---------
Other comprehensive loss ($128,398) $9,318 ($137,716)
========= ====== =========
Foreign currency translation adjustments are not recorded net-of-tax because such
adjustments relate to permanent investments in international subsidiaries.
Note 9. Recently Issued Accounting Standards
------------------------------------
In July 2001, the Financial Accounting Standards Board issued
Statement Nos. 141 and 142. The new standards require the following:
o SFAS No. 141, Business Combinations, requires that all business
combinations initiated after June 30, 2001 be accounted for using
the purchase method; the pooling method of accounting has been
eliminated. SFAS No. 141 supersedes Accounting Principles Board
(APB) Opinion No. 16, Business Combinations, but does not change
many of the provisions of APB Opinion 16, including the basic
principles of the purchase method.
o SFAS No. 142, Goodwill and Other Intangibles, supersedes APB
Opinion No. 17, Intangible Assets, and addresses how intangible
assets that are acquired individually or with a group of other
assets should be accounted for in financial statements upon their
acquisition. The statement also addresses how goodwill and other
intangibles should be accounted for after they have been
initially recognized in the financial statements. With the
adoption of SFAS No. 142, goodwill is no longer amortized over
its estimated useful life, but is subject to at least an annual
assessment for impairment by applying a fair-value-based test.
The Company will adopt SFAS No. 142 as of January 1, 2002.
In accordance with the adoption of SFAS No. 142, as of January 1,
2002, the Company will cease amortizing goodwill and other intangibles
which will result in estimated lower annual Selling, general and
administrative expenses of approximately $163.0 million ($154.0
million after-tax or $0.12 per share-diluted). The Company is
currently assessing the impact the adoption of the additional
requirements of SFAS No. 142 may have on its financial position,
results of operations and cash flows.
13
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
Results of Operations
- ---------------------
Effective January 1, 2000, the financial results of Immunex, which previously
were consolidated in the financial results of the Company, were deconsolidated
and included in the financial results of the Company on an equity basis.
Accordingly, alliance revenue relating to co-promotion agreements between the
Company and Immunex was included in pharmaceutical net revenue for both the 2001
and 2000 second quarter and first half. The 2000 second quarter and first half
financial results were restated to reflect the deconsolidation of Immunex, which
had no effect on income from continuing operations. In addition, the Company
early adopted new authoritative accounting guidance as of January 1, 2001
reflecting certain rebates and sales incentives (i.e., coupons and other rebate
programs) as reductions of revenues instead of selling and marketing expenses.
Financial information for all prior periods presented has been reclassified to
comply with the income statement classification requirements of the new
guidance. These reclassifications had no effect on total net revenue growth
between the periods presented.
Worldwide net revenue for the 2001 second quarter and first half were 6% and 7%
higher, respectively, compared with prior year levels. The increase in worldwide
net revenue for the 2001 second quarter and first half was due primarily to
higher worldwide net revenue of human pharmaceuticals, with consumer health care
also contributing revenue growth for the 2001 second quarter. Excluding the
negative impact of foreign exchange, worldwide net revenue increased 10% for the
2001 second quarter and 11% for the 2001 first half.
The following table sets forth worldwide net revenue results by operating
segment together with the percentage changes from the comparable period in the
prior year:
Net Revenue
-------------------------
Three Months
Ended June 30,
($ in millions) -------------------------
Operating Segment 2001 2000 % Increase
- -------------------- -------- -------- ----------
Pharmaceuticals $2,694.0 $2,523.3 7%
Consumer Health Care 522.4 502.9 4%
-------- -------- ----------
Total $3,216.4 $3,026.2 6%
======== ======== ==========
Net Revenue
-------------------------
Six Months
Ended June 30,
($ in millions) -------------------------
Operating Segment 2001 2000 % Increase
- -------------------- -------- -------- ----------
Pharmaceuticals $5,573.3 $5,126.3 9%
Consumer Health Care 1,092.3 1,095.8 -
-------- -------- ----------
Total $6,665.6 $6,222.1 7%
======== ======== ==========
14
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
Pharmaceuticals
- ---------------
Worldwide pharmaceutical net revenue increased 7% for the 2001 second quarter
and 9% for the 2001 first half due primarily to higher sales of human
pharmaceuticals offset, in part, by decreased sales of animal health products.
Excluding the negative impact of foreign exchange, worldwide pharmaceutical net
revenue increased 11% for the 2001 second quarter and 13% for the 2001 first
half.
Worldwide human pharmaceutical net revenue increased 8% for the 2001 second
quarter and 10% for the 2001 first half due primarily to higher sales of PREVNAR
(introduced in the 2000 first quarter), PROTONIX (introduced in the 2000 second
quarter), PREMARIN products and EFFEXOR XR offset, in part, by lower sales of
MENINGITEC, ZIAC (due to generic competition) and oral contraceptives (2001
first half only). Excluding the negative impact of foreign exchange, worldwide
human pharmaceutical net revenue increased 12% for the 2001 second quarter and
14% for the 2001 first half. MENINGITEC, the Company's meningococcal meningitis
vaccine, was launched in the United Kingdom in the fourth quarter of 1999 as the
first vaccine for this disease. The Company successfully obtained a majority of
the meningococcal meningitis vaccine market, with a significant volume of sales
occurring in the 2000 first quarter, and by the end of 2000, most children and
adolescents in the United Kingdom had been vaccinated by this product. The
product is currently being launched in ten other European countries; however,
the Company does not currently anticipate that any of these markets,
individually, will provide sales volume equivalent to that generated in the
United Kingdom.
Worldwide animal health net revenue decreased 9% for the 2001 second quarter and
7% for the 2001 first half due primarily to a decline in the United States
livestock market causing a reduction in the use of certain animal health
biological and pharmaceutical cattle products. Also contributing to the decline
in animal health product revenues was lower demand for certain pharmaceutical
cattle products internationally resulting from the outbreak of foot-and-mouth
disease and the continued concerns about mad-cow disease. The decrease in
revenues was partially offset by the domestic launch, in June 2001, of
ProHeart 6, a new single dose, canine heartworm protection product that provides
six months of continuous heartworm protection. Excluding the negative impact of
foreign exchange, worldwide animal health net revenue decreased 6% and 3% for
the 2001 second quarter and first half, respectively.
Consumer Health Care
- --------------------
Worldwide consumer health care net revenue increased 4% for the 2001 second
quarter and was flat for the 2001 first half. The increase in the 2001 second
quarter was due primarily to higher sales of CENTRUM products, ADVIL,
cough/cold/allergy products and CHAP STICK offset, in part, by lower sales of
FLEXAGEN. The same factors affected the 2001 first half; however, lower sales of
CENTRUM products and ADVIL in the 2001 first quarter contributed to the flat
results for the first half. Excluding the negative impact of foreign exchange,
worldwide consumer health care net revenue increased 7% and 2% for the 2001
second quarter and first half, respectively.
The following table sets forth, the percentage changes in worldwide net revenue
by operating segment compared to the prior year, including the effect volume,
price and foreign exchange had on these percentage changes:
15
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
% Increase (Decrease) % Increase (Decrease)
Three Months Ended June 30, 2001 Six Months Ended June 30, 2001
------------------------------------------ ------------------------------------------
Foreign Total Foreign Total
Volume Price Exchange Net Revenue Volume Price Exchange Net Revenue
------ ----- -------- ----------- ------ ----- -------- -----------
Pharmaceuticals
- --------------------
United States 9% 4% - 13% 14% 4% - 18%
International 6% 1% (8%) (1%) 4% - (8%) (4%)
--- --- --- --- --- --- --- ---
Total 8% 3% (4%) 7% 10% 3% (4%) 9%
=== === === === === === === ===
Consumer Health Care
- --------------------
United States 9% 1% - 10% 1% 2% - 3%
International (5%) 6% (8%) (7%) (3%) 4% (8%) (7%)
--- --- --- --- --- --- --- ---
Total 4% 3% (3%) 4% (1%) 3% (2%) -
=== === === === === === === ===
Total
- --------------------
United States 9% 4% - 13% 11% 4% - 15%
International 4% 2% (8%) (2%) 3% 1% (8%) (4%)
--- --- --- --- --- --- --- ---
Total 7% 3% (4%) 6% 8% 3% (4%) 7%
=== === === === === === === ===
Cost of goods sold, as a percentage of Net revenue, decreased to 24.6% for the
2001 second quarter compared to 25.5% for the 2000 second quarter and decreased
to 23.8% for the 2001 first half compared to 25.0% for the 2000 first half.
These decreases were due primarily to a favorable product mix in the
pharmaceuticals segment, as well as a small impact relating to increased
alliance revenue recorded in 2001 net revenue compared to 2000 net revenue.
There are no costs of goods sold relating to alliance revenue, and therefore any
net revenue fluctuations impacted by alliance revenues will also impact gross
margins.
Selling, general and administrative expenses increased 4% for the 2001 second
quarter and 7% for the 2001 first half. Higher expenses were due primarily to
higher selling and marketing expenses, including increased headcount, related to
recent pharmaceutical product launches and direct-to-consumer promotional costs
for significant established pharmaceutical products.
Research and development expenses increased 16% for the 2001 second quarter and
13% for the 2001 first half due primarily to increased headcount and other
research operating expenses, including higher chemical and material costs, and
cost sharing expenditures from pharmaceutical collaborations commencing in 2000
offset, in part, by lower payments under licensing agreements.
Interest expense, net decreased 5% for the 2001 second quarter and 48% for the
2001 first half, despite the rise in weighted average debt levels. The decrease
in Interest expense, net was due primarily to lower interest expense as a result
of favorable interest rates on the debt outstanding, primarily commercial paper,
16
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
as well as higher capitalized interest, resulting from additional capital
projects, recognized during the 2001 second quarter and first half compared with
the same periods in the prior year. In addition, the Company generated higher
interest income due to higher average levels of cash and marketable securities
throughout the 2001 second quarter and first half compared to prior year levels.
The Company currently anticipates higher interest expense for both the 2001
third quarter and full year, due to higher weighted average long-term debt
levels compared to the same periods in the prior year. Weighted average
long-term debt outstanding during the 2001 and 2000 second quarters was $7,511.6
million and $4,910.9 million, respectively. Weighted average long-term debt
outstanding during the 2001 and 2000 first half was $5,720.8 million and
$4,887.2 million, respectively.
The following table sets forth worldwide income from continuing operations
before taxes by operating segment together with the percentage changes from the
comparable periods in the prior year:
Income from Continuing Operations
Before Taxes (1)
------------------------------------------------------------------------------------
Three Months Six Months
Ended June 30, Ended June 30,
--------------------------------------- ----------------------------------------
($ in millions) % Increase
Operating Segment 2001 2000 (Decrease) 2001 2000 % Increase
- -------------------- ------ ------ ---------- -------- -------- ----------
Pharmaceuticals $601.2 $549.0 10% $1,516.7 $1,293.0 17%
Consumer Health Care 112.1 96.9 16% 236.1 227.4 4%
------ ------ ---- -------- -------- ----
713.3 645.9 10% 1,752.8 1,520.4 15%
Corporate (2) (81.4) (91.4) (11%) (139.9) 1,600.5 -
------ ------ ---- -------- -------- ----
Total (3) $631.9 $554.5 14% $1,612.9 $3,120.9 -
====== ====== ==== ======== ======== ====
(1) The second quarter results included goodwill amortization for 2001 and 2000 as follows: Pharmaceuticals -
$34.1 and $36.7, and Consumer Health Care - $5.9 and $8.0, respectively.
The first half results included goodwill amortization for 2001 and 2000 as follows: Pharmaceuticals -
$68.7 and $75.6, and Consumer Health Care - $11.9 and $16.0, respectively.
(2) Corporate expenses for the 2000 first half included income of $1,709.4 resulting from the receipt of a
$1,800.0 termination fee provided for under the merger agreement with Warner-Lambert Company offset, in
part, by certain related expenses. Excluding the termination fee, Corporate expenses, net increased 28%
for the 2001 first half.
(3) Excluding the termination fee, total income from continuing operations before taxes increased 14% for
the 2001 first half.
Worldwide pharmaceutical income from continuing operations before taxes
increased 10% (16% for human pharmaceuticals) for the 2001 second quarter and
17% (21% for human pharmaceuticals) for the 2001 first half due primarily to
increased worldwide sales of human pharmaceuticals and higher other income, net
offset, in part, by higher selling, general and administrative expenses and
research and development expenses.
17
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
The Company experienced a higher growth rate of worldwide pharmaceutical income
from continuing operations before taxes (17%) than the growth rate of net
revenue (9%) during the 2001 first half due primarily to improved margins
relating to the human pharmaceutical product mix, increased gains on sales of
non-strategic assets, higher equity income relating to Immunex and 2000 first
half other expenses that were non-recurring in 2001.
Worldwide consumer health care income from continuing operations before taxes
increased 16% for the 2001 second quarter and 4% for the 2001 first half. The
2001 second quarter increase was due primarily to higher worldwide consumer
health care sales and slightly improved gross margins. The Company experienced a
higher growth rate of worldwide consumer health care income from continuing
operations before taxes (16%) than the growth rate of net revenue (4%) during
the 2001 second quarter due primarily to certain asset write-offs in the 2000
first half that were non-recurring in 2001.
Corporate expenses, net, decreased 11% for the 2001 second quarter due primarily
to lower general and administrative expenses. Corporate expenses, net, excluding
the Warner-Lambert Company termination fee, increased 28% for the 2001 first
half due primarily to lower other income relating to a one-time insurance
recovery of environmental costs recorded in the 2000 first quarter offset, in
part, by lower interest expense in the 2001 first half.
The effective tax rate of continuing operations decreased to 24.5% for the 2001
second quarter compared with 25.6% for the 2000 second quarter. The effective
tax rate decreased to 24.9% for the 2001 first half compared to 25.8% for the
2000 first half (excluding the effect of the Warner-Lambert Company termination
fee). The tax rate reduction occurring in the 2001 second quarter and first half
was due primarily to an increased benefit from products manufactured in lower
taxed jurisdictions.
Consolidated Income and Diluted Earnings Per Share Results
- ----------------------------------------------------------
Income and diluted earnings per share from continuing operations for the 2001
second quarter both increased by 16% to $477.0 million and $0.36 compared to
$412.7 million and $0.31, respectively, for the prior year. The increases in
income and diluted earnings per share from continuing operations for the 2001
second quarter were due to additional worldwide sales of human pharmaceuticals
and, to a lesser extent, consumer health care products offset, in part, by
higher selling, general and administrative expenses, and research and
development expenses.
Income and diluted earnings per share from continuing operations for the 2001
first half increased 16% and 15%, respectively, to $1,210.6 million and $0.91
compared to $1,047.6 million and $0.79, respectively, for the same period last
year (excluding the Warner-Lambert Company termination fee). Income and diluted
earnings per share from continuing operations for the 2000 first half included
income of $1,111.1 million and $0.84, respectively, resulting from the Warner-
Lambert Company termination fee. The increases in income and diluted earnings
18
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
per share from continuing operations for the 2001 first half were due primarily
to additional worldwide sales of human pharmaceuticals and lower interest
expense offset, in part, by higher selling, general and administrative
expenses, and research and development expenses.
Euro Currency
- -------------
As of January 1, 2001, 12 of the 15 member countries of the European Union
adopted the Euro as a new common legal currency. However, the legacy currencies
of the member countries are scheduled to remain legal tender as
sub-denominations of the Euro until January 1, 2002 (the transition period).
Critical areas impacted by the conversion to the Euro have been identified and
appropriate strategies developed, which are currently being implemented to
facilitate the adoption of the Euro and to facilitate business transactions
during the transition period. The costs related to the Euro conversion and
transition period will not have a material adverse effect on the Company's
financial position, results of operations or cash flows. However, the conversion
to the Euro may have competitive implications on the Company's pricing and
marketing strategies, the total impact of which is not known at this time.
Competition and Manufacturing
- -----------------------------
The Company operates in the highly competitive pharmaceutical and consumer
health care industries. The Company is not dependent on any one patent-protected
product or line of products for a substantial portion of its net revenue or
results of operations. PREMARIN, the Company's principal conjugated estrogens
product manufactured from pregnant mare's urine, and related products PREMPRO
and PREMPHASE (which are single tablet combinations of the conjugated estrogens
in PREMARIN and the progestin medroxyprogesterone acetate), are the leaders in
their categories and contribute significantly to net revenue and results of
operations. PREMARIN's natural composition is not subject to patent protection
(although PREMPRO has patent protection). The principal uses of PREMARIN,
PREMPRO and PREMPHASE are to manage the symptoms of menopause and to prevent
osteoporosis, a condition involving a loss of bone mass in postmenopausal women.
Estrogen-containing products manufactured by other companies have been marketed
for many years for the treatment of menopausal symptoms, and several of these
products also have an approved indication for the prevention of osteoporosis.
During the past several years, other manufacturers have introduced products for
the treatment and/or prevention of osteoporosis. New products containing
different estrogens than those found in PREMPRO and PREMPHASE and having many
forms of the same indications have also been introduced. Some companies have
attempted to obtain approval for generic versions of PREMARIN. These products,
if approved, would be routinely substitutable for PREMARIN and related products
under many state laws and third-party insurance payer plans. In May 1997, the
U.S. Food and Drug Administration (FDA) announced that it would not approve
certain synthetic estrogen products as generic equivalents of PREMARIN given
known compositional differences between the active ingredient of these products
and PREMARIN. Although the FDA has not approved any generic equivalent to
PREMARIN to date, PREMARIN will continue to be subject to competition from
existing and new competing estrogen and other products for its approved
19
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
indications and may be subject to generic competition from either synthetic or
natural conjugated estrogens products in the future. At least one other company
has announced that it is in the process of developing a generic version of
PREMARIN from the same natural source, and the Company currently cannot predict
the timing or outcome of these or any other efforts.
The Company has been experiencing inconsistent results on dissolution testing of
certain dosage forms of PREMARIN and is working with the FDA to resolve this
issue. Until this issue is resolved, supply shortages of one or more dosage
strengths may occur. Although these shortages may adversely affect PREMARIN
sales in one or more reporting periods, the Company believes that, as a result
of current inventory levels and the Company's enhanced process controls, testing
protocols and ongoing formulation improvement project, overall PREMARIN Family
sales will not be significantly impacted.
Liquidity, Financial Condition and Capital Resources
- ----------------------------------------------------
The Company generated operating cash inflows totaling $1,995.7 million during
the 2001 first half due primarily to income from continuing operations,
collections on accounts receivables and timing of certain selling programs, and
favorable timing of payments made on accounts payables and accrued expenses.
These cash inflows were more than offset by an increase in inventories of $229.3
million and payments of $5,948.9 million relating to the diet drug litigation
(see Note 3 to the Consolidated Condensed Financial Statements).
The Company used $1,372.4 million of cash for investments in property, plant and
equipment and marketable securities. The capital expenditures made during the
2001 first half were consistent with the Company's commitment to expand existing
manufacturing and research and development facilities worldwide, and build new
biotechnology facilities. The Company received investment proceeds through the
sales and maturities of marketable securities and the sales of non-strategic
assets totaling $367.6 million.
As described in Note 1 to the Consolidated Condensed Financial Statements, the
Company obtained new credit facilities totaling $6,000.0 million in March 2001.
The new credit facilities include a $3,000.0 million, 364-day credit facility
(which support borrowings under the commercial paper program). Any borrowings
actually drawn from the credit facility are extendible for an additional year.
In addition, the new credit facilities included a $3,000.0 million, 364-day
bridge facility, which facility was terminated when the Company issued $3,000.0
million of Notes on March 30, 2001. On March 30, 2001, the Company issued three
tranches of Notes in a transaction exempt from registration under the Securities
Act pursuant to Rule 144A, as follows:
o $500.0 million, 5.875% Notes due March 15, 2004
o $1,000.0 million, 6.25% Notes due March 15, 2006
o $1,500.0 million, 6.70% Notes due March 15, 2011
The interest rate payable on each series of Notes is subject to an increase of
.25 percentage points per level of downgrade in the Company's credit rating by
Moody's and Standard & Poor's. However, the total adjustment to the interest
rate for the series of Notes cannot exceed two percentage points. The Company
would incur a total of approximately $7.5 million of additional annual interest
expenses for every .25 percentage point increase in the interest rate. If
Moody's and Standard & Poor's subsequently increase the Company's credit rating,
the interest rate payable on each series of Notes is subject to a decrease of
.25 percentage points for each level of increase. The interest rate payable for
the series of Notes cannot be reduced below the original coupon rate of each
series of Notes. There is no adjustment to the interest rate payable on each
series of Notes for the first single level downgrade in the Company's credit
rating by Standard & Poor's. Any interest rate increase or decrease, as
described herein, will take effect from the first day of the interest period
during which a ratings change requires an adjustment in the interest rate. In
the case of the $1,500.0 million, 6.70% Notes, the interest rate in effect on
March 15, 2006 for such Notes will, thereafter, become the effective interest
rate until maturity on March 15, 2011.
20
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
The $3,000.0 million, 364-day facility is combined with the Company's existing
$2,000.0 million five-year credit facility (termination date of July 31, 2002)
to provide $5,000.0 million of credit facilities to support the Company's
commercial paper program. The Company offers its commercial paper in a very
liquid market commensurate with its long term credit ratings from Moody's (A3)
and Standard & Poor's (single-A). The net proceeds received from the combined
Notes and commercial paper supported by the credit facilities totaled $5,626.4
million. The Company is using the proceeds from the Notes and commercial paper
supported by the credit facilities for general corporate and working capital
requirements, including the capital expenditures identified above, and payments
related to the REDUX and PONDIMIN diet drug litigation.
The Company also used cash for financing activities related to dividend payments
of $604.4 million, which was partially offset by $128.9 million of cash provided
by stock option exercises.
Management remains confident that cash flows from operating activities and
available financing resources will be adequate to fund the Company's operations,
pay opt out settlement payments and fund the nationwide, class action settlement
relating to the REDUX and PONDIMIN diet drug litigation, pay dividends, maintain
the ongoing programs of capital expenditures, and repay both the principal and
interest on its outstanding obligations, without requiring the disposition of
any significant strategic core businesses.
Quantitative and Qualitative Disclosures about Market Risk
- ----------------------------------------------------------
The market risk disclosures appearing in the Company's 2000 Annual Report on
Form 10-K have not materially changed from December 31, 2000 except as follows:
o In conjunction with the Notes issued by the Company on March 30, 2001,
the Company entered into interest rate swap agreements related to the
$1,500.0 million 6.70% Notes due March 15, 2011.
o The interest rate swap agreements are contracts under which the
Company converted the fixed rate of the $1,500.0 million 6.70% Notes
to a floating rate of interest over the term of the interest rate swap
agreements, which is the same term as the underlying debt.
21
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
o The interest rate swap agreements are effective fair value hedges, as
the terms of the interest rate swaps are the same as the underlying
debt and therefore the current market interest rate fluctuations on
the debt will be completely offset by the effectiveness of the
interest rate swap.
At June 30, 2001, the fair values of the Company's financial instruments were as
follows:
($ in millions) Notional/
Description Contract Amount Carrying Value Fair Value
--------------------- --------------- -------------- ----------
Forward contracts (1) $514.4 $15.2 $15.2
Option contracts (1) 583.2 26.5 26.5
Interest rate swaps 1,500.0 (40.7) (40.7)
Outstanding debt (2) 8,119.5 8,075.4 8,158.6
(1) If the value of the U.S. dollar were to increase or decrease by 10%, in
relation to all hedged foreign currencies, the net receivable on the
forward and option contracts would decrease or increase by
approximately $71.2 million.
(2) If the interest rates were to increase or decrease by one percentage
point, the fair value of the outstanding debt would increase or
decrease by approximately $222.5 million.
The estimated fair values approximate amounts at which these financial
instruments could be exchanged in a current transaction between willing parties.
Therefore, fair values are based on estimates using present value and other
valuation techniques that are significantly affected by the assumptions used
concerning the amount and timing of estimated future cash flows and discount
rates that reflect varying degrees of risk. Specifically, the fair value of
forward contracts and interest rate swaps reflects the present value of the
future potential gain or (loss) if settlement were to take place on June 30,
2001; the fair value of option contracts reflects the present value of future
cash flows if the contracts were settled on June 30, 2001; and the fair value of
outstanding debt instruments reflects a current yield valuation based on
observed market prices as of June 30, 2001.
ENBREL Supply
- -------------
ENBREL is a biological treatment for juvenile, early stage and moderate to
severe rheumatoid arthritis. ENBREL was discovered by Immunex and is being
co-promoted in North America by Immunex and the Company. The Company has
exclusive marketing rights to ENBREL outside of North America. Although the
market demand for ENBREL is increasing, the sales growth is currently
constrained by limits on the existing source of supply. This is anticipated to
continue until the retrofitting of a Rhode Island facility is completed and
approved, which is targeted to occur in the second half of 2002. There can be no
assurance, however, that any estimated date will prove to be accurate. If the
market demand continues to grow, there may be further supply constraints even
after the Rhode Island facility begins producing ENBREL. The current plan for
the longer term includes a new manufacturing facility, which is being
constructed in Ireland.
22
Management's Discussion and Analysis of Financial Condition
and Results of Operations
Three Months and Six Months Ended June 30, 2001
Cautionary Statements for Forward-Looking Information
- -----------------------------------------------------
This Form 10-Q, including management's discussion and analysis set forth above,
contains certain forward-looking statements, including, among other things,
statements regarding the Company's results of operations, Euro currency,
competition, liquidity, financial condition and capital resources, PREMARIN,
ENBREL supply, MENINGITEC sales, foreign currency and interest rate risk, the
nationwide, class action settlement relating to REDUX and PONDIMIN, and
additional litigation charges related to REDUX and PONDIMIN including those for
opt outs. These forward-looking statements are based on current expectations of
future events that involve risks and uncertainties including, without
limitation, risks associated with the inherent uncertainty of pharmaceutical
research, product development, manufacturing, and commercialization, economic
conditions including interest and currency exchange rate fluctuations, the
impact of competitive or generic products, product liability and other types of
lawsuits, the impact of legislative and regulatory compliance and obtaining
approvals, and patents. The Company assumes no obligation to publicly update any
forward-looking statements, whether as a result of new information, future
events or otherwise. Certain factors which could cause the Company's actual
results to differ materially from expected and historical results have been
identified by the Company in Exhibit 99 to the Company's 2000 Annual Report on
Form 10-K, which exhibit is incorporated herein by reference.
23
Part II - Other Information
Item 1. Legal Proceedings
-----------------
The Company and its subsidiaries are parties to numerous lawsuits and
claims arising out of the conduct of its business, including product
liability and other tort claims, the most significant of which are
described in the Company's Annual Report on Form 10-K for the year
ended December 31, 2000 and Quarterly Report on Form 10-Q for the
period ended March 31, 2001.
On July 10, 2001, the District Court of Jim Wells County, Texas for
the 79th Judicial District entered a final judgment in the case of
Lopez v. American Home Products Corporation, et al., No. 99-07-37723.
The jury in the Lopez case had returned a verdict in favor of the
plaintiff in April 2001 for $11.55 million in compensatory damages and
$45 million in punitive damages for injuries allegedly sustained by
the plaintiff due to her use of PONDIMIN. In entering the final
judgment, the court applied the Texas statutory cap on punitive
damages and granted the plaintiff's request to voluntarily remit
certain amounts awarded as compensatory damages. The final judgment
included approximately $4.8 million in compensatory damages, $3.4
million in punitive damages and $1 million in pre-judgment interest,
for a total of approximately $9 million. The Company intends to pursue
an appeal from the final judgment.
The Company continues to resolve the remaining claims of those
individuals who have opted out of the Company's nationwide, class
action settlement of the diet drug litigation involving PONDIMIN
and/or REDUX (see Note 3 to the Consolidated Condensed Financial
Statements).
In the litigation involving the Company's DIMETAPP and ROBITUSSIN
cough/cold products that contained the ingredient phenylpropanolamine
("PPA"), one additional class action has been filed. Sims, et al. v.
The Delaco Company f/k/a/ Thompson Medical Co., Inc., et al., No.
3-01-0509 (U.S.D.C., M.D. Tenn.), is a putative class action against
the Company and seven other defendants seeking economic damages, a
court-supervised medical monitoring program and a court-supervised
educational program to fully apprise plaintiffs and class members of
the alleged adverse health effects and risks of PPA. In addition to
the Sims case and the previously reported putative class actions,
there are a total of 62 individual personal injury lawsuits against
the Company that have been filed alleging injury as a result of
ingestion of PPA-containing products. The Company expects that
additional PPA cases may be filed in the future against it and the
other companies that marketed PPA-containing products. The Company
intends to defend all such cases vigorously.
In University of Colorado et al. v. American Cyanamid Company,
described in the Annual Report on Form 10-K, a trial on potential
damages was held in March 2001 and, in July 2001, the District Court
awarded plaintiffs damages of approximately $24 million, together with
pre-judgment interest, bringing the damages award to between
approximately $45 million and $55 million. The Company intends to
appeal the damages award to the U.S. Court of Appeals for the Federal
Circuit.
24
A purported class action on behalf of "end-payors" (defined as the
last persons and entities in the chain of distribution) was filed in
federal district court in Cincinnati, alleging that the Company
violated federal and state antitrust laws through alleged exclusionary
practices relating to PREMARIN and that these practices resulted in
unjust enrichment. (Mattoon, et al. v. Wyeth-Ayerst Laboratories,
U.S.D.C. W.D., No. C-1-01447, July 6, 2001.) The relief requested
includes injunctive relief, damages and disgorgement of profits. The
Company intends to vigorously defend this action.
In the Brand Name Prescription Drugs Antitrust Litigation MDL 997, the
Company settled the complaint brought by Rite Aid, Revco and certain
other pharmacies for an undisclosed amount that is not material to the
Company.
In the litigation relating to the settlement by the Company of a
patent dispute with Schering-Plough Corporation regarding the
Company's proposed generic version of Schering's K-Dur potassium
chloride supplement product, a total of approximately 35 purported
class actions have been filed in various federal and state courts,
primarily on behalf of alleged classes of indirect purchasers. The
allegations in these cases are similar to the allegations in the FTC
complaint in In the Matter of Schering-Plough Corp. et al., Docket No.
9297. The complaints challenge as violations of federal and state
antitrust and/or consumer protection laws the Company's agreement with
Schering-Plough to settle a patent case that alleged that the
Company's generic version of Schering's K-Dur product infringed
Schering's valid patent. The relief sought includes treble damages,
disgorgement and injunctive relief. The Company believes that its
settlement with Schering-Plough did not violate the FTC Act or the
antitrust laws and intends to vigorously defend these cases.
In the opinion of the Company, although the outcome of any legal
proceedings cannot be predicted with certainty, the ultimate liability
of the Company in connection with its legal proceedings will not have
a material adverse effect on the Company's financial position but
could be material to the results of operations in any one accounting
period.
25
Item 4. Submission of Matters to a Vote of Security-Holders
---------------------------------------------------
(a) The matters described under item 4(c) below were submitted to a
vote of security-holders, through the solicitation of proxies
pursuant to Section 14 under the Securities Exchange Act of 1934,
as amended, at the Annual Meeting of Stockholders held on April
26, 2001 (the "Annual Meeting").
(b) Not applicable.
(c) The following describes the matters voted upon at the Annual
Meeting and sets forth the number of votes cast for, against or
withheld and the number of abstentions as to each such matter
(there were no broker non-votes):
(i) Election of directors:
Nominee For Withheld
--------------------------- -------------- ----------
Clifford L. Alexander, Jr. 1,107,244,048 10,821,999
Frank A. Bennack, Jr. 1,107,643,370 10,422,677
Richard L. Carrion 1,107,142,864 10,923,183
Robert Essner 1,107,992,740 10,073,307
John D. Feerick 1,107,626,669 10,439,378
John P. Mascotte 1,107,759,835 10,306,212
Mary Lake Polan, M.D., Ph.D 1,107,891,670 10,174,377
Ivan G. Seidenberg 1,079,861,533 38,204,514
Walter V. Shipley 1,107,599,744 10,471,091
John R. Stafford 1,107,298,696 10,767,351
John R. Torell III 1,107,808,864 10,257,183
(ii) Ratification of the appointment of Arthur Andersen LLP as
principal independent public accountants for 2001:
For Against Abstain
------------- ---------- ---------
1,094,252,290 18,720,484 4,517,957
26
Item 6. Exhibits and Reports on Form 8-K
--------------------------------
(a) Exhibits
--------
Exhibit No. Description
----------- -----------
(10.1) American Home Products Corporation Deferred
Compensation Plan as amended to date.
(10.2) American Home Products Corporation Stock Option
Plan for Non-Employee Directors as amended to
date.
(10.3) American Home Products Corporation 1994
Restricted Stock Plan For Non-Employee Directors
as amended to date.
(10.4) American Home Products Corporation Directors'
Deferral Plan as amended to date.
(12) Computation of Ratio of Earnings to Fixed Charges.
(b) Reports on Form 8-K
-------------------
None
27
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.
AMERICAN HOME PRODUCTS CORPORATION
----------------------------------
(Registrant)
By /s/ Paul J. Jones
------------------------------
Paul J. Jones
Vice President and Comptroller
(Duly Authorized Signatory
and Chief Accounting Officer)
Date: August 14, 2001
28
Exhibit Index
-------------
Exhibit No. Description
- ---------- -----------
(10.1) American Home Products Corporation Deferred
Compensation Plan as amended to date.
(10.2) American Home Products Corporation Stock Option
Plan for Non-Employee Directors as amended to
date.
(10.3) American Home Products Corporation 1994
Restricted Stock Plan For Non-Employee Directors
as amended to date.
(10.4) American Home Products Corporation Directors'
Deferral Plan as amended to date.
(12) Computation of Ratio of Earnings to Fixed Charges.
EX-1