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10-Q/APeriod: Q1 FY2003

JOHNSON & JOHNSON Quarterly Report (Amendment) for Q1 Ended Mar 30, 2003

Filed May 15, 2003For Securities:JNJ

Summary

Johnson & Johnson (JNJ) reported strong first-quarter 2003 results, with worldwide sales increasing by 12.3% to $9.8 billion, driven by robust performance across its Consumer, Pharmaceutical, and Medical Devices & Diagnostics segments. Net earnings rose 12.9% to $2.1 billion, or $0.69 per diluted share, reflecting a 16.9% increase from the prior year's first quarter. The company also demonstrated effective management of its financial resources, with operating cash flow of $2.0 billion and a continued commitment to shareholder returns through an increased dividend, marking the 41st consecutive annual increase. The company strategically expanded its portfolio through several key acquisitions, including those of Orquest, Inc., Orapharma, Inc., and 3-Dimensional Pharmaceuticals, Inc., all aimed at enhancing its pipeline in areas like orthopaedics, specialty pharmaceuticals, and early-stage drug development for cardiovascular and inflammatory diseases. Significant forward-looking investments were made in anticipation of new product launches, such as the CYPHER drug-eluting stent, with substantial R&D charges expected in the second quarter related to the acquisition of Scios, Inc.

Key Highlights

  • 1Worldwide sales grew 12.3% to $9.8 billion in Q1 2003, with international sales up 18.2% (11.3% from currency).
  • 2Net earnings increased 12.9% to $2.1 billion, resulting in a 16.9% rise in diluted EPS to $0.69.
  • 3Operating cash flow was strong at $2.0 billion for the quarter.
  • 4The company declared a regular cash dividend of $0.24 per share, a 17.1% increase, marking the 41st consecutive annual dividend increase.
  • 5Strategic acquisitions were made, including Orquest, Orapharma, and 3-Dimensional Pharmaceuticals, bolstering the company's innovation pipeline.
  • 6Significant R&D charges are anticipated in Q2 2003 related to the acquisition of Scios, Inc. ($700-800 million pre-tax) and Link Spine Group, Inc. ($175 million pre-tax).
  • 7The CYPHER drug-eluting coronary stent received FDA approval and began shipping, aiming to reduce restenosis.

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