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ηγωεϊ εδεγςεϊ μςιϊεπεϊθας ξεγιςδ ςμ χαμϊ ΰιωεψ ξεϊπδ μιιφεψ εωιεεχ θαμιεϊ ®REQUIP30/11/2007 θας ξεγιςδ διεν λι χιαμδ ΰιωεψ ξεϊπδ ξψωεϊ δξζεο εδϊψετεϊ δΰξψιχΰιϊ (FDA) μιιφεψ εωιεεχ δβψρδ δβπψιϊ ωμ θαμιεϊ (®Requip (Ropinirole HCl ωμ ηαψϊ GlaxoSmithKline, αξιπεπιν ωμ 0.25 ξ"β αριρ, 0.5 ξ"β αριρ, 1 ξ"β αριρ, 2 ξ"β αριρ, 3 ξ"β αριρ, 4 ξ"β αριρ ε- 5 ξ"β αριρ. ΰιωεψ ρετι ωμ θαμιεϊ Ropinirole HCl ωμ θας φτει μδϊχαμ ςν ϊτεβϊ δβπϊ δτθπθ μξεφψ δξχεψι α- 19 αξΰι, 2008. ςν χαμϊ δΰιωεψ δρετι, δξεφψ ωμ θας ιδιδ δβψρδ δβπψιϊ ωμ θαμιεϊ ®Requip. δϊλωιψ ξεϊεεδ μθιτεμ αριξπιν εαϊρξιπιν ωμ ξημϊ δτψχιπρεο ωριαϊδ ΰιπδ ιγεςδ ελο ΰεωψ μθιτεμ αϊρξεπϊ ψΰωεπιϊ, ξϊεπδ ςγ ηξεψδ, ωμ "δψβμ δςφαπιϊ" (RESTLESS LEG). μξεφψ δξχεψι διε ξλιψεϊ ωπϊιεϊ ωμ λ- 455 ξμιεο $ αΰψδ"α αωπιν ςωψ δηεγωιν ωδρϊιιξε α- 30 αρτθξαψ, 2007, αδϊαρρ ςμ πϊεπι IMS. ΰεγεϊ θας θας ϊςωιεϊ τψξφαθιεϊ ας"ξ διπδ ηαψδ βμεαμιϊ ωαριρδ αιωψΰμ εΰηϊ ξ- 20 δηαψεϊ δτψξφαθιεϊ δξεαιμεϊ αςεμν. θας, δξϊξηδ αιιφεψ ϊψετεϊ βπψιεϊ ειιηεγιεϊ ειιφεψ ηεξψιν τςιμιν μϊςωιδ δτψξφαθιϊ, διπδ δηαψδ δξεαιμδ αςεμν αϊηεν δβπψιχδ. μθας ΰϊψι ιιφεψ, ξηχψ, ωιεεχ εδτφδ αιωψΰμ, αφτεο εαξψλζ ΰξψιχδ εαΰιψετδ. ιεϊψ ξ- 80% ξξλιψεϊιδ ωμ δχαεφδ δο μφτεο ΰξψιχδ εΰιψετδ. This release contains forward-looking statements, which express the current beliefs and expectations of management. Such statements are based on managements current beliefs and expectations and involve a number of known and unknown risks and uncertainties that could cause Tevas future results, performance or achievements to differ significantly from the results, performance or achievements expressed or implied by such forward-looking statements. Important factors that could cause or contribute to such differences include risks relating to: Teva`s ability to successfully develop and commercialize additional pharmaceutical products, the introduction of competing generic equivalents, the extent to which Teva may obtain U.S. market exclusivity for certain of its new generic products and regulatory changes that may prevent Teva from utilizing exclusivity periods, competition from brand-name companies that are under increased pressure to counter generic products, or competitors that seek to delay the introduction of generic products, the impact of consolidation of our distributors and customers, potential liability for sales of generic products prior to a final resolution of outstanding patent litigation, including that relating to the generic versions of Allegra® Neurontin® and Lotrel®, the effects of competition on our innovative products, especially Copaxone® sales, the impact of pharmaceutical industry regulation and pending legislation that could affect the pharmaceutical industry, the difficulty of predicting U.S. Food and Drug Administration, European Medicines Agency and other regulatory authority approvals, the regulatory environment and changes in the health policies and structures of various countries, our ability to achieve expected results though our innovative R&D efforts, Tevas ability to successfully identify, consummate and integrate acquisitions, potential exposure to product liability claims to the extent not covered by insurance, dependence on the effectiveness of our patents and other protections for innovative products, significant operations worldwide that may be adversely affected by terrorism, political or economical instability or major hostilities, supply interruptions or delays that could result from the complex manufacturing of our products and our global supply chain, environmental risks, fluctuations in currency, exchange and interest rates, and other factors that are discussed in Tevas Annual Report on Form 20-F and its other filings with the U.S. Securities and Exchange Commission. Forward-looking statements speak only as of the date on which they are made and the Company undertakes no obligation to update or revise any forward-looking statement, whether as a result of new information, future events or otherwise. In this press release, we present certain as adjusted numbers, which are non-GAAP financial measures. These numbers exclude items such as the effects of step-up of inventory upon acquisition, acquisition of R&D in process, product rights impairment, restructuring expenses, settlements and related tax effect. A reconciliation between the as adjusted numbers and the comparable GAAP measures is included later in this release. We provide such non-GAAP data because we believe that such supplemental data provide useful information to investors to better understand underlying trends in our business. However, adjusted financial measures are not, and should not be, viewed as a substitute for GAAP results. Our definition of these adjusted financial measures may differ from similarly named measures used by others.
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