J. Pearson
Analyst · RBC Capital Markets
Good morning, everyone for the third time. Hopefully, third time's a charm. We'll start from the beginning.
As you've read in our press release, we followed up our solid performance in the first half of 2013 with another quarter of strong operating results. On today's call, I will review our third quarter results and performance, provide an update on Valeant's business and then provide my open perspectives in Bausch + Lomb. Howard will then provide an update on the Bausch + Lomb integration and discuss the business going forward. After our remarks, Howard and I will be available for Q&A.
This morning, we reported Valeant's third quarter results for 2013, which were driven by strong sales growth and profitability across all of our businesses, including strong performance from Bausch + Lomb since the August 5 close.
Total revenue in the quarter was $1.54 billion as compared to $884 million in the third quarter of 2012. Our third quarter cash EPS was $1.43 per share. As a reminder, we closed the Bausch + Lomb financing before we closed the deal. The pre-closing interest expense and the pre-closing impact of our additional shares cost us $0.09 per share. If you exclude this cost, our cash EPS increased 31% this quarter.
In addition, foreign exchange movement negatively impacted us by $0.03 in the quarter and an unexpected early generic launch of Retin-A Micro that occurred right after our last earnings call in August, had a negative $0.04 impact on the third quarter results. All these negatives are included in the $1.43 cash EPS.
Adjusted cash flow from operations was $408 million for the quarter, an increase of 69% over the prior year.
I would like to take a moment to touch on several onetime items that were also recorded during the quarter. First, we took a total impairment charge of $645 million for the retigabine and ezogabine franchise. This charge was necessitated by the decision by GSK to cease marketing and sales support for the IR foreign relation in the U.S..
In addition, we announced earlier this week that we have settled all outstanding claims by Anacor Pharmaceuticals regarding Jublia and all other disputes with Anacor for $142.5 million.
Finally, we recorded $305 million of restructuring and integration charges, primarily related to the Bausch + Lomb acquisition.
As we mentioned in August, post the Bausch + Lomb acquisition, we have a very diversified portfolio of Rx, device, OTC and brand generics businesses. We will continue our strategy of focusing on long-lived durable products, cash pay businesses and growth geographies. We do not want to limit ourselves to 1 or 2 therapeutic areas but rather, we look for durable products that could be actively promoted to a small set of physicians or health care professionals to drive strong organic growth.
As you can see from the chart, branded prescription drugs now represent 41% of our total pro forma 2013 revenues. Of this revenue slice, only 24% of the brand prescriptions sales, or 10% of our total revenue, are subject to a patent cliff. We believe our strategy has positioned us with the most durable set of assets in the industry.
This dynamic is further demonstrated by the patent chart that we shared with you last quarter. Looking forward over the next 4 years, you can see that 2013 is, by far, our toughest year, as we were impacted by generic competition for Zovirax, Retin-A Micro and a number of other brands.
The year-on-year impact and lost revenues will be $300 million in 2013. A significant impact on our total revenue base of approximately $6 billion. We will also expect patent expiry on Vanos in the U.S. and Wellbutrin in Canada during the fourth quarter.
With our most recent acquisitions, including Bausch + Lomb, and other promoted brands coupled with the significant increase in third-party promotion of many of our neuro and other products, our U.S. business mix has changed significantly. Today, 80% of our U.S. products are now actively promoted through sales forces, directed physician marketing and other targeted selling activities. Going forward, our percentage of promoted products in the U.S. will only increase given the number of new product launches we have planned for 2014 and beyond. Therefore, it no longer makes sense to split the U.S. market into promoted and non-promoted products for the purpose of reporting organic growth. I would also like to note that with the addition of Bausch + Lomb, coupled with the acquisition of Obagi and the significant growth of our aesthetics businesses, our U.S. business is even more diversified.
For example, our prescription dermatology business in the U.S. now only represents 20% of our U.S. revenues, a dramatic shift from just a year ago.
Given the impact of generics on the Zovirax franchise, Retin-A Micro, and BenzaClin. We thought it would be more useful to our investors to show organic growth excluding these products to demonstrate the growth of the underlying business. The decline of revenue of the above-mentioned products was approximately $100 million for the quarter, and the details are included in table 6 of our press release for your information.
As we move forward, we will continue to show organic growth without the impact of significant generics, and also to disclose the quarterly revenue impact of products excluded from the calculation. We believe that this presentation will facilitate investors in modeling their revenues going forward.
Excluding these products, our U.S. business continues to exhibit solid organic growth of 5%, driven by many of our dermatology prescription brands, our aesthetics and oral health portfolios and our Orphan drug products and Xenazine. Our emerging market segment delivered the same-store organic growth rate of 14% in the quarter, continuing the exceptional strong progress seen so far this year.
Almost all the legacy Valeant U.S. business reported strong performance this quarter. While the overall U.S. Dermatology market continues to realize greater generic penetration, most of our brands have continued to maintain or growing market share including Elidel, Acanya, Atralin, Carac and CeraVe, just to name a few. Solodyn, while seeing some erosion this year, appears to have stabilized at roughly $200 million on an annualized level.
Our aesthetics franchise continues to perform extremely well. Dysport continues to increase its market share and Obagi had another great quarter. We attribute this continued progress to our commitment to the specialty, our continued development of relationships with many doctors and our broad portfolio. Our MVP Program has been very well received, as we continue to pay benefits. We are very excited about the future of this business.
OraPharma continues its strong performance track record, once again, with double-digit revenue growth. We will introduce a new product to support bone regeneration post-tooth removal in Q4 which should further boost growth going forward.
Finally, our neuro and other portfolio saw a double-digit growth in our Orphan drug portfolio and we are pleased to say that Wellbutrin XL continued to be stable at approximately $150 million annually.
The legacy generic products that are partnered with Teva and Forest continued their decline, but now represent only about $50 million a year.
As we noted on the organic growth chart, our Emerging Markets continue to deliver strong growth. Our operations in Central and Eastern Europe remained robust growing at a healthy 15% rate with both Russia and Poland significantly outpacing their respective markets. We are now a top 10 player in Poland and we have well north of $400 million in revenue in Russia.
Our operations in Southeast Asia and South Africa also remained very strong with same-store sales nearing 20% organic growth. We are excited to have entered Vietnam and with the close of the Euvipharm acquisition and we are looking to establish a local presence in Indonesia within the next 12 months.
Latin America also recorded double-digit growth in the quarter with both our Mexican and Brazilian businesses continuing their track record of strong growth.
Finally, a few reflections on the Bausch + Lomb acquisition. Since the transaction closed in August, I've spent a significant amount of time getting to know our operations and people around the world. I've been to Germany, France, the U.K., Sweden, Eastern Europe, China, Japan, Mexico, Canada and all of our locations in the U.S. multiple times. Probably, the best word I can use to sum of these travels is, excited. I'm excited about our new colleagues and I'm very pleased with the continued strong performance of the business during the integration process. I'm excited about the opportunity to streamline costs and to trim the fat without touching the muscle. The global and regional Bausch + Lomb infrastructure was inappropriate given the size of the business.
In fact, we should be able to exceed our synergy targets. I'm excited about our decentralized launch feed that has been embraced across the organization. I am convinced that better decisions will be made by people closer to the customers. And I'm most excited about the opportunity to adopt local business strategies and foresee local business development activities. I am convinced that we will accelerate our growth, by giving our country teams more say in how products are positioned and priced, and how they can be complemented by new products such as lower-cost surgical equipment, to meet local needs.
Finally, I am excited about the continued productivity of the Bausch + Lomb development team. Since we announced the deal, we have had 8 new product approvals and many more are on the way. As expected, our R&D spend will be higher in the first half of 2014 as multiple Phase III pharmaceutical programs will be reaching completion. We did not include any of these development programs in our deal model. We would hope some will succeed, so we can deliver more upside to all of you.
With that, I will turn the call over to over to Howard.