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ηγωεϊ εδεγςεϊ μςιϊεπεϊ

γ"ψ τιμιτ τψερθ, ρβο ιε"ψ θας, ξεπδ μϊτχιγ ιε"ψ δγιψχθεψιεο

09/03/2010
θας δεγιςδ διεν λι ξψ ΰμι δεψαιυ δεγις μγιψχθεψιεο δηαψδ ςμ ψφεπε μδωϊηψψ ξϊτχιγιε αηαψδ ςμ ξπϊ ωιελμ μδϊξχγ αδημξϊε. μΰηψ γιεπιν ωδϊχιιξε διεν αγιψχθεψιεο εαδϊΰν μδξμφϊ εςγϊ δξιπειιν ωμ δηαψδ, δγιψχθεψιεο δημιθ τδ ΰηγ μξπεϊ ΰϊ δξωπδ μιε"ψ δγιψχθεψιεο, γ"ψ τιμιτ τψερθ, μϊτχιγ ιε"ψ δγιψχθεψιεο.

αδϊΰν μλκ, δρϊιιξδ λδεπϊε ωμ τψετ' ξωδ ξπι λιε"ψ δζξπι ωμ δγιψχθεψιεο εδγιψχθεψιεο δημιθ τδ ΰηγ μξπεϊ ΰϊ δτψετ' ξπι μϊτχιγ δξωπδ μιε"ψ δγιψχθεψιεο.

αδϊιιηρ μξιπειε, ΰξψ γ"ψ τψερθ λι "δπριαεϊ ΰωψ δεαιμε μδϊτϊηειεϊ δΰηψεπεϊ ξςφιαεϊ ΰϊ λεμπε. ΰμι δεψαιυ ξιμΰ ϊτχιγ ιιηεγι εξωξςεϊι αδϊτϊηεϊδ ωμ θας αξωκ ωπιν ψαεϊ εηαψι δγιψχθεψιεο λξε βν λμ ςεαγι θας ξΰημιν με δημξδ ξμΰδ εξδιψδ ".

γ"ψ τψερθ δξωικ εΰξψ λι "ϊηϊ δπδβϊε ωμ ωμξδ ιπΰι, πωιΰ εξπλ"μ θας, δηαψδ δϊτϊηδ αΰετο ξψωιν αξωκ ωμεω δωπιν δΰηψεπεϊ. λιε"ψ, ΰπι ξϊλεεο ιηγ ςν ηαψιι αγιψχθεψιεο, μδωχις ΰϊ ξιψα δξΰξφιν ςμ ξπϊ μριις μωμξδ εμδπδμϊ δηαψδ αηϊιψδ μδωβϊ διςγιν δΰρθψθβιιν ΰωψ ΰεωψε αγιψχθεψιεο δηαψδ εδεφβε αΰηψεπδ μωεχ δδεο. ΰπι ςεξγ μημεθιο ξΰηεψι ξηειαεϊιπε μδξωικ μδπδιβ ΰϊ ωεχ δβπψιχδ δβμεαμι ξδξψλζ δπιδεμι ωμπε αιωψΰμ".

γ"ψ τιμιτ τψερθ (73) ξωξω λξωπδ μιε"ψ δγιψχθεψιεο ωμ θας ξΰζ ιπεΰψ 2006, μΰηψ ψλιωϊδ ωμ ηαψϊ ΰιεεχρ ςμ ιγι θας. αιο δωπιν 1987-2006, μτπι ξιπειε μγιψχθεψιεο ωμ θας γ"ψ τψερθ ωιξω λιε"ψ δγιψχθεψιεο ελξπλ"μ ηαψϊ ΰιεεχρ. γ"ψ τψερθ ξωξω λιεν λιε"ψ δγιψχθεψιεο ελξπλ"μ ηαψϊ δτψξφαθιχδ Opko Health Inc., λιε"ψ ωμ ηαψϊ Prolor Biotech Inc. ωξψλζδ αιωψΰμ ελο λιε"ψ ωμ Landenburg Thalmann Financial Services. απερσ γ"ψ τψερθ δεΰ ξωχις ξψλζι αξρτψ ηαψεϊ ιωψΰμιεϊ αςιχψ αϊηεν δαιεξγ. γ"ψ τψερθ ξωξω βν λγιψχθεψ ωμ ηαψϊ Continucare Corporation Inc., εωμ ηαψϊ Castle Brands Inc.. δεΰ ξωξω ΰσ ληαψ αγιψχθεψιεο ωμ δ-Regents of the Smithsonian Institution. λξε λο, γ"ψ τψερθ ιεωα αηαψ δπΰξπιν ωμ δ- Scripps Research Institute ελο αηαψ δπΰξπιν ωμ ΰεπιαψριθϊ ξιΰξι. μγ"ψ τψερθ BA αρτψεϊ φψτϊιϊ ξΰεπιαψριθϊ τπρμαπιδ ξ-1957 ελο M.D. ξξλμμϊ ΰμαψθ ΰιιπωθιιο μψτεΰδ ξ-1961.

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 μϊςωιιδ 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.
Teva’s Safe Harbor Statement under the U. S. Private Securities Litigation Reform Act of 1995:
This release contains forward-looking statements, which express the current beliefs and expectations of management. Such statements are based on management's current beliefs and expectations and involve a number of known and unknown risks and uncertainties that could cause our 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: our ability to successfully develop and commercialize additional pharmaceutical products, the introduction of competing generic equivalents, the extent to which we may obtain U.S. market exclusivity for certain of our new generic products and regulatory changes that may prevent us from utilizing exclusivity periods, potential liability for sales of generic products prior to a final resolution of outstanding patent litigation, including that relating to the generic versions of Neurontin®, Lotrel®, Protonix® and Eloxatin®, the current economic conditions, 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 effects of competition on our innovative products, especially Copaxone® sales, dependence on the effectiveness of our patents and other protections for innovative products, the impact of consolidation of our distributors and customers, the impact of pharmaceutical industry regulation and pending legislation that could affect the pharmaceutical industry, our ability to achieve expected results through our innovative R&D efforts, the difficulty of predicting U.S. Food and Drug Administration, European Medicines Agency and other regulatory authority approvals, the uncertainty surrounding the legislative and regulatory pathway for the registration and approval of biotechnology-based products, the regulatory environment and changes in the health policies and structures of various countries, supply interruptions or delays that could result from the complex manufacturing of our products and our global supply chain, our ability to successfully identify, consummate and integrate acquisitions, the potential exposure to product liability claims to the extent not covered by insurance, our exposure to fluctuations in currency, exchange and interest rates, significant operations worldwide that may be adversely affected by terrorism, political or economical instability or major hostilities, our ability to enter into patent litigation settlements and the intensified scrutiny by the U.S. government, the termination or expiration of governmental programs and tax benefits, impairment of intangible assets and goodwill, environmental risks, and other factors that are discussed in this report and in our other filings with the U.S. Securities and Exchange Commission ("SEC").
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