Teva Completes Generic Pulmicort® Respules Portfolio with the Launch of Third Strength in the United States
09 Mars 2016 - 5:33PM
Business Wire
Teva Pharmaceutical Industries Ltd. (NYSE: TEVA) today announced
the launch of the generic equivalent to Pulmicort Respules®1
(budesonide inhalation suspension), 1 mg/2 mL, in the United
States.
Budesonide inhalation suspension is an inhaled corticosteroid
medicine. It is a long-term maintenance medicine used to control
and prevent asthma symptoms in children ages 12 months to 8 years.
Budesonide inhalation suspension helps to reduce swelling and
inflammation in the lungs, and also helps keep the airways open to
reduce asthma symptoms.
With the addition of this new strength of budesonide inhalation
suspension, Teva—the leader of the product market in total
prescriptions of budesonide inhalation suspension2—now offers the
complete family of all strengths including, 0.25 mg/2 mL, 0.5 mg/2
mL, and 1 mg/2 mL.
Pulmicort Respules® (budesonide inhalation suspension), had
annual sales of approximately $217 million in the United States,
according to IMS data as of November 2015.
About Budesonide Inhalation Suspension
Budesonide inhalation suspension is indicated for the
maintenance treatment of asthma and as prophylactic therapy in
children 12 months to 8 years of age. Budesonide inhalation
suspension is not indicated for the relief of acute
bronchospasm.
Important Safety Information
The use of budesonide inhalation suspension is contraindicated
in the primary treatment of status asthmaticus or other acute
episodes of asthma where intensive measures are required.
Budesonide inhalation suspension is contraindicated in patients
with hypersensitivity to budesonide or any of the ingredients of
budesonide inhalation suspension.
Systemic and inhaled corticosteroid use may result in the
following serious adverse reactions: Candida albicans infection;
hypersensitivity reactions, including anaphylaxis;
immunosuppression; hypercorticism and adrenal suppression;
reduction in bone mineral density; growth effects in pediatric
patients; glaucoma, increased intraocular pressure and cataracts;
and eosinophilic conditions and Churg-Strauss syndrome.
The most common adverse reactions (incidence ≥ 3%) in clinical
trials were: respiratory infection, rhinitis, coughing, otitis
media, viral infection, moniliasis, gastroenteritis, vomiting,
diarrhea, abdominal pain, ear infection, epistaxis, conjunctivitis,
and rash.
For more information, please see the accompanying Full
Prescribing Information.
1 Pulmicort Respules® is a registered trademark of AstraZeneca
group of companies. 2 IMS data, as of 11/15.
About Teva
Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) is a
leading global pharmaceutical company that delivers high-quality,
patient-centric healthcare solutions used by millions of patients
every day. Headquartered in Israel, Teva is the world’s largest
generic medicines producer, leveraging its portfolio of more than
1,000 molecules to produce a wide range of generic products in
nearly every therapeutic area. In specialty medicines, Teva has a
world-leading position in innovative treatments for disorders of
the central nervous system, including pain, as well as a strong
portfolio of respiratory products. Teva integrates its generics and
specialty capabilities in its global research and development
division to create new ways of addressing unmet patient needs by
combining drug development capabilities with devices, services and
technologies. Teva's net revenues in 2015 amounted to $19.7
billion. For more information, visit www.tevapharm.com.
Teva's Safe Harbor Statement under the U. S. Private
Securities Litigation Reform Act of 1995:
This release contains forward-looking statements, which 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 develop and commercialize
additional pharmaceutical products; competition for our specialty
products, especially Copaxone® (which faces competition from
orally-administered alternatives and a generic version); our
ability to consummate the acquisition of Allergan plc’s worldwide
generic pharmaceuticals business (“Actavis Generics”) and to
realize the anticipated benefits of such acquisition (and the
timing of realizing such benefits); the fact that following the
consummation of the Actavis Generics acquisition, we will be
dependent to a much larger extent than previously on our generic
pharmaceutical business; potential restrictions on our ability to
engage in additional transactions or incur additional indebtedness
as a result of the substantial amount of debt we will incur to
finance the Actavis Generics acquisition; the fact that for a
period of time following the consummation of the Actavis Generics
acquisition, we will have significantly less cash on hand than
previously, which could adversely affect our ability to grow; the
possibility of material fines, penalties and other sanctions and
other adverse consequences arising out of our ongoing FCPA
investigations and related matters; our ability to achieve expected
results from investments in our pipeline of specialty and other
products; our ability to identify and successfully bid for suitable
acquisition targets or licensing opportunities, or to consummate
and integrate acquisitions; the extent to which any manufacturing
or quality control problems damage our reputation for quality
production and require costly remediation; increased government
scrutiny in both the U.S. and Europe of our patent settlement
agreements; our exposure to currency fluctuations and restrictions
as well as credit risks; the effectiveness of our patents,
confidentiality agreements and other measures to protect the
intellectual property rights of our specialty medicines; the
effects of reforms in healthcare regulation and pharmaceutical
pricing, reimbursement and coverage; competition for our generic
products, both from other pharmaceutical companies and as a result
of increased governmental pricing pressures; governmental
investigations into sales and marketing practices, particularly for
our specialty pharmaceutical products; adverse effects of political
or economic instability, major hostilities or acts of terrorism on
our significant worldwide operations; interruptions in our supply
chain or problems with internal or third-party information
technology systems that adversely affect our complex manufacturing
processes; significant disruptions of our information technology
systems or breaches of our data security; competition for our
specialty pharmaceutical businesses from companies with greater
resources and capabilities; the impact of continuing consolidation
of our distributors and customers; decreased opportunities to
obtain U.S. market exclusivity for significant new generic
products; potential liability in the U.S., Europe and other markets
for sales of generic products prior to a final resolution of
outstanding patent litigation; our potential exposure to product
liability claims that are not covered by insurance; any failure to
recruit or retain key personnel, or to attract additional executive
and managerial talent; any failures to comply with complex Medicare
and Medicaid reporting and payment obligations; significant
impairment charges relating to intangible assets, goodwill and
property, plant and equipment; the effects of increased leverage
and our resulting reliance on access to the capital markets;
potentially significant increases in tax liabilities; the effect on
our overall effective tax rate of the termination or expiration of
governmental programs or tax benefits, or of a change in our
business; variations in patent laws that may adversely affect our
ability to manufacture our products in the most efficient manner;
environmental risks; and other factors that are discussed in our
Annual Report on Form 20-F for the year ended December 31, 2015 and
in our other filings with the U.S. Securities and Exchange
Commission (the "SEC"). Forward-looking statements speak only as of
the date on which they are made and we assume no obligation to
update or revise any forward-looking statements or other
information, whether as a result of new information, future events
or otherwise.
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Teva Pharmaceutical Industries Ltd.IR Contacts:Kevin C.
Mannix, United States, 215-591-8912Ran Meir, United
States, 215-591-3033Tomer Amitai, Israel 972 (3)
926-7656orPR Contacts:Iris Beck Codner, Israel, 972 (3)
926-7687Denise Bradley, United States, 215-591-8974Nancy
Leone, United States, 215-284-0213
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