March is Colorectal Cancer Awareness Month

March is Colorectal Cancer Awareness Month. The VDH Cancer Prevention and Control Program works to decrease the burden of colorectal and other cancers through helping to develop and promote evidence-based strategies shown to prevent and control cancer. Colorectal cancer (CRC) is the second leading cause of cancer death. However, CRC screening makes dying from this disease preventable. During this month, we want to continue to spread the message that CRC is “Preventable. Treatable. Beatable!”

Colorectal cancer is cancer that occurs in the colon or rectum. It is also called colon cancer, for short. Sometimes abnormal growths, called polyps, form in the colon or rectum. Over time, some polyps may turn into cancer. Screening tests can find polyps so they can be removed before turning into cancer. Screening also helps find colorectal cancer at an early stage, when treatment works best.

To learn more about decreasing CRC risks, visit this page at the Centers for Disease Control and Prevention (CDC):

Statement from FDA Commissioner on New Data Demonstrating Rising Youth Use of Tobacco Products and the Agency’s Ongoing Actions to Confront the Epidemic of Youth E-cigarette Use

Feb. 11, 2019 – In his statement below that was released by U.S. Food and Drug Administration (FDA) Commissioner Scott Gottlieb, M.D., he discusses new data demonstrating rising youth use of tobacco products and the Agency’s ongoing actions to confront the epidemic of youth e-cigarette use.

“Today, the U.S. Centers for Disease Control and Prevention (CDC) released additional data from our joint FDA/CDC 2018 National Youth Tobacco Survey. These data are a sobering reminder of the initial results we shared last fall indicating a rampant rise of youth e-cigarette use, which has prompted the FDA to take a series of escalating regulatory actions as part of our Youth Tobacco Prevention Plan. We are advancing those actions, and committing to some new steps. The epidemic use of e-cigarettes among children is one of the biggest public health challenges currently facing the FDA.

According to the data released today, approximately 4.9 million middle and high school students were current users (used in the past 30 days) of some type of tobacco product in 2018, up from 3.6 million in 2017. This increase is driven by an alarming surge in e-cigarette use. More than 3.6 million middle and high school students were current (past 30 day) e-cigarette users in 2018, a dramatic increase of more than 1.5 million students in one year. The study authors suggest — as the FDA also noted at the time of the initial release of this data in the fall – that the rise in e-cigarette use in the last year is likely due to the recent popularity of certain types of e-cigarettes, such as JUUL. Further, youth who use e-cigarettes also are using them more frequently and using flavored products more often than last year. Many youth tobacco product users are also using multiple products. Among current tobacco users, about 2 in 5 (1.68 million) high school students and 1 in 3 (270,000) middle school students used two or more tobacco products in 2018. The most commonly used tobacco product combination was e-cigarettes and conventional cigarettes among both middle and high school students.

Similarly, data from the recent National Institutes of Health’s Monitoring the Future study found comparable trends: From 2017 to 2018, current (past 30-day) e-cigarette use reportedly increased from 6.6 percent to 10.4 percent among 8th grade students; 13.1 percent to 21.7 percent among 10th grade students; and 16.6 percent to 26.7 percent among 12th grade students. In other words, more than a quarter of 12th graders in the U.S. are using e-cigarettes—exposing them to harmful effects of nicotine and other chemicals and putting them at risk of transitioning to other tobacco products.

These risks were further reinforced in research recently published in JAMA Network Open, which showed that, compared with non-users, youth who use e-cigarettes are more likely to transition to conventional cigarettes ‒ risking a lifetime of addiction to smoking and resulting smoking-attributable disease and erasing the reductions in youth smoking rates that we’ve achieved in America. The bottom line is that kids using e-cigarettes aren’t kids who “would have smoked cigarettes.” Quite the opposite. As a society, we’ve made great strides in stigmatizing cigarette use among kids. The kids using e-cigarettes are children who rejected conventional cigarettes, but don’t see the same stigma associated with the use of e-cigarettes. But now, having become exposed to nicotine through e-cigs, they will be more likely to smoke. I will not allow a generation of children to become addicted to nicotine through e-cigarettes. We must stop the trends of youth e-cigarette use from continuing to build and will take whatever action is necessary to ensure these kids don’t become future smokers.

Based on a growing body of evidence, I fear the youth trends will continue in 2019, forcing us to make some tough decisions about the regulatory status of e-cigarettes. The signs that we’re seeing are not encouraging. They point to continued growth in youth use of these products. No child should be using any tobacco or nicotine-containing product. We’ll continue to take steps to try to investigate the root causes of this spike in youth e-cigarette use and arrest the momentum of these trends, in particular, by ensuring these products are sold in ways that make them less accessible and appealing to youth. But, if these youth use trends continue, we’ll be forced to consider regulatory steps that could constrain or even foreclose the opportunities for currently addicted adult smokers to have the same level of access to these products that they now enjoy. I recognize that such a move could come with significant impacts to adult smokers. The FDA has repeatedly affirmed our collective view that e-cigarettes may have promise as a tool for helping currently addicted adult smokers quit smoking. But, with the staggering data on youth trends, we’re struggling to preserve these opportunities for adults while addressing the youth epidemic. I simply won’t allow their sale to come at the expense of addicting a generation of kids to nicotine.

To help address this growing use among kids, over the past year, the FDA has taken a rigorous enforcement stance, including a number of actions to combat the illegal sales of e-cigarettes to youth through our enforcement efforts at brick-and-mortar and internet storefronts, as well as taken steps to target companies engaged in kid-friendly marketing that increases the appeal of these products to youth. I’ve also appealed to the companies responsible for many of these products, and met with senior executives from five of the largest manufacturers of e-cigarette products. In addition, last week, I sent letters to the chief executive officers of Altria Group Inc. and JUUL Labs Inc. asking to meet with them to discuss my concerns that they don’t seem fully committed to their written promises about the steps they’d take to stop youth use of their products.

Just last week, the FDA escalated enforcement action against certain local Walgreens and Circle K retail locations for repeatedly selling tobacco products to minors by filing a complaint seeking to bar the two specific retail locations from selling tobacco products for 30 days. As part of that effort we’re also writing the corporate management of a number of large, national retail chains to discuss whether there is a corporate-wide issue related to their stores’ non-compliance and put them on notice that the FDA is considering additional corporate-wide enforcement avenues to address violative tobacco sales to youth, which have also included illegal sales of e-cigarettes to kids. This past fall, we marked a historic milestone of conducting a total of one million tobacco retailer inspections since we began doing so in 2010. To commemorate this, we’re sending letters to governors and agencies across the country thanking them for their work to support our efforts to protect youth – and reminding them of the need for continued vigilance to make sure retailers aren’t selling tobacco products to minors.

Beyond enforcement and social responsibility, we’ve committed to meaningful policy changes. Notably, in November, I announced proposed new steps to protect youth by preventing access to flavored tobacco products, including e-cigarettes. This policy framework will both address the disturbing trend of youth e-cigarette use and advance the historic declines we’ve achieved in recent years in the rates of combustible cigarette use among kids. This framework reflects a re-doubling of the FDA’s efforts to protect kids from all nicotine-containing products. It also reflects a very careful public health balance between steps to enable the opportunities to transition to non-combustible products to be available for adults; and our solemn mandate to make nicotine products less accessible and less appealing to children. In other words – a balance between closing the on-ramp for kids to become addicted to nicotine through combustible and non-combustible products, while maintaining the off ramp for adults through access to potentially less harmful forms of nicotine delivery for adult smokers seeking to transition away from combustible tobacco products.

Evidence shows that minors are especially attracted to flavored e-cigarette products, and that youth access these products from both brick and mortar retailers as well as online. With that in mind, we’re revisiting our compliance policy that has resulted in certain e-cigarettes, including flavored e-cigarettes, remaining on the market until 2022 while their manufacturers submit applications for premarket authorization. In particular, as I announced on Nov. 15, 2018, the FDA is revisiting the compliance policy on premarket tobacco product application authorization for all flavored e-cigarette products other than tobacco, mint, and menthol, sold in physical locations where people under the age of 18 are permitted. For example, this would include e-cigarettes or electronic nicotine delivery system (ENDS) products, such as e-liquids, cartridge-based systems, and cigalikes, in fruit and candy flavors like cherry, vanilla, crème, tropical, melon and others. In addition, we will seek to curtail the sale of applicable flavored ENDS products that are sold online without heightened age verification processes.

We’ll be providing further information on these policies soon. If data continue to show upwards trends in youth use of tobacco products, we’ll continue to refine our policies as necessary, taking additional steps to strengthen our response.

More recently, we’ve undertaken efforts to further the discussion and understanding around how we can help aid those kids who are already addicted to the nicotine in e-cigarettes quit. This includes holding a public hearing to discuss efforts to eliminate youth e-cigarette use as well as other tobacco product use, with a focus on the potential role of drug therapies to support cessation and the issues impacting the development of such therapies for youth. Already, I’ve heard too many troubling stories from parents of teenagers, pediatricians, and young people themselves about the effects of this epidemic. The stories make clear that, for many young e-cigarette users, addiction has already taken hold.

We’ve also launched “The Real Cost” Youth E-Cigarette Prevention Campaign – a new, comprehensive effort targets nearly 10.7 million youth, aged 12-17, who have used e-cigarettes or are open to trying them. The new campaign features hard-hitting advertising on digital and social media sites popular among teens, as well as posters with e-cigarette prevention messages in high schools across the nation. The new e-cigarette prevention effort builds off the FDA’s first youth tobacco prevention campaign, “The Real Cost,” which launched in 2014 to reduce teen cigarette smoking. In its first two years, the youth smoking prevention campaign prevented nearly 350,000 teens from initiating cigarette smoking and resulted in savings of more than $31 billion for youth, their families and society at large by reducing smoking-related costs like early loss of life, costly medical care, lost wages, lower productivity and increased disability. The success of “The Real Cost” campaign suggests that our other tobacco prevention campaigns, including our campaign on youth use of e-cigarettes, can build on this success as we strive to reduce the number of kids who use tobacco products.

As part of the youth e-cigarette prevention campaign, we also joined forces with Scholastic to expand distribution of youth e-cigarette prevention posters to every public and private high school in the U.S. and released new resources for doctors, youth groups, churches, state and local public health agencies, and others on the dangers of youth e-cigarette use. Additionally, our work with Scholastic to provide educators with resources to help them engage with students about e-cigarette use has helped reach more than 2.7 million students so far. We’ve also received very positive teacher feedback on the helpfulness of these resources. Vaping remains a top issue at some schools, but teachers are reporting that vaping on campus has declined after using these resources on the dangers of youth e-cigarette use.

While these efforts are a good start, we recognize they’re not enough. This is an exploding epidemic. We’ll continue to put the full scope of our regulatory tools against this mounting public health crisis. We’re considering some new steps for 2019.

Moving forward, the FDA has a number of actions planned and we’ll have more to say on these and other actions very soon. We’re continuing our stepped-up enforcement actions with a sustained campaign to monitor, penalize and prevent e-cigarette sales to minors in retail locations, including manufacturers’ internet storefronts. The agency is also exploring action under both its civil and criminal enforcement tools to target potentially violative sales and marketing practices by manufacturers as well as retailers. We’re also investigating counterfeit e-cigarette products. In addition to our meeting with Altria and JUUL, we also plan to meet with state attorneys general to discuss how they can help combat youth e-cigarette use in their states. We’re also exploring how we can partner with others to look at opportunities to work together around these shared goals. These are just some of the additional steps that we’re taking.

The numbers are clear – we’re experiencing epidemic-level rises in youth e-cigarette use, which is threatening the progress we’ve made toward reducing youth tobacco use. These trends require forceful and sometimes unprecedented action among regulators, public health officials, manufacturers, retailers and others to address this troubling problem. Our commitment to stemming the epidemic of youth e-cigarette use has not waivered, but we know there’s more to be done by all parties.”

The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.”

This message is broadcasted by the Division of Communications in FDA’s Office of Regulatory Affairs (ORA).


People in 19 states exposed to Brucella bacteria from drinking raw milk

Food Safety News
Feb. 11, 2019
By Coral Beach
QUARRYVILLE, Pa. — Although it’s illegal to sell unpasteurized milk across state lines, federal officials say people in 19 states have been exposed to drug-resistant Brucella after consuming raw milk from Miller’s Biodiversity Farm in Pennsylvania. In a nationwide food safety alert, the Centers for Disease Control and Prevention warned that anyone who has consumed raw dairy products from the farm in the past three years should check in with their doctors. The outbreak strain of Brucella — RB51 — is resistant to rifampin, one of the antibiotics that is typically be used to prevent or treat brucellosis. The CDC and state officials are urging consumers to throw away any raw dairy products from Miller’s Biodiversity Farm that they have in their homes.  … Investigators have discovered people in 19 states bought or consumed raw milk from the Pennsylvania farm. The CDC alert did not report how the unpasteurized, raw milk had been illegally transported or sold across state lines. The 19 states are Alabama, California, Connecticut, Florida, Georgia, Iowa, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Rhode Island, South Carolina, and Virginia.

Learn more:

Tris Pharma, Inc Expands Its Voluntary Nationwide Retail Recall of Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 mL, Due to Higher Concentration of Ibuprofen

January 29, 2019 – Monmouth Junction, NJ, Tris Pharma, Inc. is expanding the scope of its November 2018 recall by adding three (3) additional lots of Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 mL, to the retail (pharmacy) level. Some units from these batches have been found to have higher levels of Ibuprofen concentration.

Infants already susceptible to the adverse effects of ibuprofen may be at a slightly higher risk if they receive medication from an impacted bottle. There is a remote probability that infants, who may be more susceptible to a higher potency level of drug, may be more vulnerable to permanent NSAID-associated renal injury. Some units from these six (6) lots have been found to contain Ibuprofen as high as 10% above the specified limit. Studies have shown that safety issues or toxicity is generally accepted to be a concern in infants at doses in excess of 700% of the recommended dose.1 To date, no serious adverse events have been reported related to this recall.

Learn more about this expanded recall:

Jac. Vandenberg, Inc. Recalls Fresh Peaches, Fresh Nectarines and Fresh Plums Because They May Be Contaminted with Listeria Monocytogenes

Jac. Vandenberg, Inc. of Yonkers, New York is recalling 1,727 cartons of Fresh Peaches, 1,207 cartons of Fresh Nectarines and 365 cartons of Fresh Plums because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The Fresh Peaches, Fresh Nectarines and Fresh Plums were distributed in Alabama, California, Georgia, Illinois, Kentucky, Maine, Massachusetts, Michigan, Mississippi, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, West Virginia and Virginia through small retail establishments and the following select retail stores, read more:

Third Case of Rifampin/Penicillin-Resistant Strain of RB51 Brucella from Consuming Raw Milk


Third Case of Rifampin/Penicillin-Resistant Strain of RB51 Brucella from Consuming Raw Milk 


The New York State Department of Health and Pennsylvania Department of Health are investigating Brucella RB51 exposures that may be connected to consuming raw (unpasteurized) milk from Miller’s Biodiversity Farm in Quarryville, Pennsylvania. Symptoms of brucellosis can include fever, sweats, malaise, anorexia, headache, fatigue, muscle and joint pain, and potentially more serious complications (e.g., endocarditis, hepatomegaly, splenomegaly, and neurologic symptoms). In pregnant patients, Brucella infections can be associated with miscarriage. Symptom onset can occur anywhere from five days to six months following exposure. As of January 22, 2019, exposures have been identified in 19 states: Alabama, California, Connecticut, Florida, Georgia, Iowa, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Rhode Island, South Carolina, and Virginia.


This investigation is associated with the third known case of brucellosis from Brucella RB51 due to raw milk acquired in the U.S., since August 2017. A New York resident, who drank raw milk purchased from Miller’s Biodiversity Farm in Quarryville, Pennsylvania, was diagnosed with brucellosis in November 2018. Milk samples from the dairy tested positive for Brucella strain RB51. People who consumed raw milk or raw milk products from this dairy since January 2016 may have been exposed.
– Patients who are still within six months of the date they last consumed the raw milk are at an increased risk for brucellosis and appropriate post-exposure prophylaxis (PEP) is recommended, along with six months of symptom monitoring. Please see diagram below.
– If patients are outside of the six-month window following their last consumption of the raw milk and have or develop an illness consistent with brucellosis, a blood culture should be obtained prior to starting any treatment, preferably while the patient is symptomatic.

Brucella strain RB51 is a live-attenuated cattle vaccine strain, which can be shed in milk and can cause infections in humans. RB51 is resistant to rifampin and penicillin. There is no serological test available to detect RB51 infection. Blood culture is the recommended diagnostic test for exposed individuals who are symptomatic.1


The Centers for Disease Control and Prevention (CDC) recommends the following:

  1. A 21-day course of both doxycycline and trimethoprim/sulfamethoxazole for first-line PEP for RB51 exposure.If brucellosis occurs despite prophylaxis, treatment should be pursued; alternative options should be considered for those with contraindications to the stated PEP and treatment regimens.Please note that RB51 is resistant to rifampin and penicillin.
  2. When ordering blood cultures to diagnose brucellosis, please advise the laboratory that blood culture may grow Brucella and that appropriate laboratory containment and precautions should be observed.3
  3. Advise patients to discard any leftover or stored, raw milk or raw milk products from this dairy farm.

Please see the diagram below for information on developing an evaluation and treatment plan for patients who consumed raw milk or raw milk products from Miller’s Biodiversity Farm since January 2016, and are still within the six-month window following their last known exposure.

Treatment Decision Tree for Patients Who Consumed Raw Milk or Raw Milk Products
from Miller’s Biodiversity Farm in Quarryville, Pennsylvania

Note: Testing for asymptomatic patients is not recommended.

Read this CDC Advisory in full at: CDC HAN 417 Third Case of Rifampin Penicillin-Resistant RB51 Brucella from Consuming Raw Milk 01.23.19

COCA Call – 2018-2019 Influenza Season and Recommendations for Clinicians

Calendar Reminder To Get A Flu ShotInfluenza activity in the United States is increasing and is expected to continue at elevated levels for several more weeks. Influenza A(H1N1)pdm09 viruses have been most common this season; influenza A(H3N2) and influenza B viruses are also circulating. In the southeastern part of the country, influenza A(H3N2) viruses have been most commonly reported this season. Annual influenza vaccination is recommended for all people 6 months and older and is the best way to prevent influenza and its potentially serious complications. Available evidence consistently indicates that antiviral treatment initiated as early as possible can be a useful second line of defense to treat influenza illness when indicated and can reduce severe outcomes of influenza.

During this CDC Clinician Outreach and Communication Activity (COCA) Call, clinicians will learn about 2018 –2019 influenza activity and hear an overview of CDC’s recommendations for health care providers regarding influenza vaccination and the use of influenza antiviral medications for the 2018-2019 influenza season, including a new antiviral medication approved by the FDA in October 2018. View complete info at:

Date: Tuesday, January 29, 2019
Time: 2:00-3:00 PM ET
A few minutes before the webinar begins, please click the link below to join the webinar:

Or iPhone one-tap:
US: +16468769923,,862187873#  or +16699006833, 862187873#

Or Telephone:
US: +1 646 876 9923  or +1 669 900 6833

Webinar ID: 862 187 873
International numbers available here:
The recordings (audio, slides, and transcript) for this call will be posted on the webpage a week after the COCA Call.
Free Continuing Education (CE) is available for most COCA Calls. Please see below for instructions on how to receive CE.

Activity Specific Objectives

At the conclusion of this COCA Call, the participant will be able to accomplish the following:

  • Summarize the current status of influenza activity in the United States.
  • Discuss the circulating influenza strains seen this season and the implications for clinicians.
  • Describe antiviral treatment recommendations for patients with influenza.

COCA Call Objectives

At the conclusion of the session, the participant will be able to accomplish the following:

  1. Cite background information on the topic covered during the presentation.
  2. Discuss CDC’s role in the topic covered during the presentation.
  3. Describe the topic’s implications for clinicians.
  4. Discuss concerns and/or issues related to preparedness for and/or response to urgent public health threats.
  5. Promote health improvement, wellness, and disease prevention in cooperation with patients, communities, at-risk populations, and other members of an interprofessional team of health care providers.


  • Alicia P. Budd, MPH
    Influenza Division
    National Center for Immunization and Respiratory Diseases
    Centers for Disease Control and Prevention
  • Angela Campbell, MD, MPH
    Medical Officer
    Influenza Division
    National Center for Immunization and Respiratory Diseases
    Centers for Disease Control and Prevention

Instructions for Obtaining Continuing Education (CE)

To receive continuing education (CE) for WC2922-012919 – (Webcast) Clinician Outreach and Communication Activity (COCA) Calls/Webinars – “2018-2019 Influenza Season and Recommendations for Clinicians” – January 29, 2019, please visit TCEO and follow these 9 Simple Steps by March 4, 2019.

To receive continuing education (CE) for WD2922-012919 – Clinician Outreach and Communication Activity (COCA) Calls/Webinars – “2018-2019 Influenza Season and Recommendations for Clinicians” – January 29, 2019, (Web on Demand), please visit TCEO and follow these 9 Simple Steps by March 5, 2021.

Norovirus Season is Here!

Virginia is seeing more visits to hospitals and clinics due to the sudden onset of symptoms of nausea, vomiting, diarrhea and stomach cramping. These illnesses are associated with the arrival of norovirus season. Norovirus is often called the “stomach flu” or the “stomach bug,” and it is on the rise. Learn the best ways to stop the spread of norovirus. Wash your hands with warm soap and water for at least 20 seconds, and stay home from work or school if ill. Learn more about norovirus infection and prevention.

Wegmans recalls cauliflower rice, stir-fry mixes due to E. coli concerns

Wegmans Food Markets is recalling cauliflower rice and vegetable stir-fry mixes sold this month in its stores in six states due to E. coli concerns. The move came just five days after a California farm involved in a recent E. coli outbreak that sickened nearly 60 people said it was recalling cauliflower and red and green lettuce. The Wegmans recall involves fresh Cauliflower Rice, Veggie Cauliflower Rice Blend and Stir-Fry Mix with Cauliflower sold between Dec. 7 and Dec. 18 at its 98 stores in New York, New Jersey, Pennsylvania, Maryland, Virginia and Massachusetts. All contain “use by” dates of Dec. 11 through Dec. 22, the company said. Learn more:

Surgeon General’s Advisory on E-cigarette Use Among Youth

Today U.S. Surgeon General Jerome Adams issued an Advisory on E-cigarette Use Among Youth at a press conference in Washington, D.C. The advisory, prompted by recent skyrocketing rates of e-cigarette use by our nation’s youth, will alert parents, teachers and health professionals about new types of e-cigarettes and the negative health consequences of youth use of these products.

E-cigarette use has recently surged among youth, fueled by new e-cigarette types that look like a USB flash drive and other shapes. One of the most commonly sold USB flash drive shaped e-cigarettes is JUUL, and other companies are now starting to sell e-cigarettes that look like USB flash drives. Most e-cigarettes contain nicotine, which can harm the developing adolescent brain.

The Surgeon General urges immediate action to protect our nation’s young people from the addiction to nicotine. The advisory encourages many different stakeholders to take action to protect our nation’s youth from this health risk, including parents, teachers, health professionals, and states, communities, tribes, and territories.

Learn more: