St. Luke’s Health System will discontinue administering the Moderna vaccine for COVID-19. The last day St. Luke’s will administer the Moderna vaccine is May 22, 2023. After that, we will either recommend that our patients receive Pfizer, or we will refer to others in the community still offering Moderna.
Moderna is being offered by many other pharmacies and health care providers in our communities. The latest findings from the Center for Disease Control and Prevention show that additional doses after the primary series can be “mixed and matched,” which means Pfizer can be used as an additional dose for those who have received either Johnson & Johnson or Moderna as a primary series.
In the past three years, vaccine changes have accelerated, and administration of multiple brands has become more complex. We believe providing one vaccine brand will increase safety for our patients and allow our staff to better manage the complex processes for multiple shots and various age groups.
Providing one vaccine brand also will allow us to implement new changes as quickly as possible and streamline shipping, storage and preparation requirements.
Pregnant women with COVID-19 can have severe illness and severe outcomes, including ICU admission, mechanical ventilation, and death.
That's why St. Luke’s OB/GYN providers recommend the COVID-19 vaccine for people who are pregnant, breastfeeding or trying to get pregnant. More than 139,000 pregnant women have enrolled in the V-Safe Pregnancy Registry. Data shows there is no risk of miscarriage associated with the vaccines.
COVID-19 vaccines do not cause infection; they do prevent severe illness from COVID-19, which is dangerous for a pregnant woman and her fetus. Maternal infection with the virus is associated with an increased risk of preterm delivery and stillbirth. Vaccinated mothers who are breastfeeding transmit antibodies that may help protect their newborns.
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Pfizer has reported that its vaccine is 95% effective in preventing COVID-19 infection, once seven days have passed since the second vaccine dose (booster shot). The Moderna vaccine is reporting a 94.5% effectiveness rate.
The COVID vaccine will help your body generate antibodies to help protect you from the virus without getting sick. Vaccines can produce longer-lasting protection than if you had the disease. Research shows antibodies in recovering adults last up to four months. The CDC says more data is needed to know how long immunity produced by the vaccination will last.
In a Pfizer trial study, the vaccine prevented the disease in 100 percent of the 1,131 adolescents who received it. Pfizer said the vaccine was well tolerated and side effects were consistent with those reported by people 16-25 years old. Our pediatricians and physicians say it is better to get the vaccine than to risk getting the disease, the symptoms and the possible long-term effects.
Please review the fact sheets for each vaccine, as developed by the manufacturers:
These are not new technologies. The vaccines are actually set up to give us immunity that is better than natural infection. We know the side effects of the natural infection. When we compare the risks to those at the frontlines that are being exposed to the virus and those in our community who are at high-risk for severe disease and death, those risks greatly overshadow the unknown risks of the vaccine.
No, it is made from a portion of the virus’ molecular material (RNA). For more information on the science behind the vaccine, please visit Centers for Disease Control and Prevention site, Understanding mRNA COVID-19 Vaccines. Also check out, Facts about COVID-19 Vaccines.
Yes, because the vaccine is 95% effective, not 100% effective. Those exposed to the virus later, after the booster vaccine, tended to have mild symptoms if they became ill at all.
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Pfizer and Moderna: The most common side effect is injection site pain. Other side effects of the Pfizer and Moderna vaccines include fatigue, headache, muscle pain and chills, and generally last two days before subsiding. These side effects indicate that the vaccine is doing its job, mimicking an infection in the body without causing a COVID-19 infection. Severe adverse reactions such as allergic reactions and Bell’s Palsy are much less common, but if they occur, need to be reported to your health care provider. None of these side effects are contagious.
It is important to note that reactions after the vaccine and the actual COVID-19 infection are significantly different. Vaccine reactions may involve some mild symptoms occurring in the first couple of days, coupled with the pain at the injection site, redness and swelling (from the vaccine), as noted above. By contrast, the COVID-19 infection reaction has a respiratory component, cough and nasal congestion, loss of taste or smell, shortness of breath, much more fever, and also a longer period of muscle pain, fatigue and headache.
Infrequently, people who have received dermal fillers may develop swelling at or near the filler injection site, usually face or lips, after receiving a dose of an mRNA COVID-19 vaccine (Pfizer or Moderna). It appears to be temporary and can resolve with medical treatment, including corticosteroid therapy. People who have received dermal fillers can be vaccinated without additional precautions but should contact their health care provider if they develop swelling afterward.
St. Luke’s will bill your insurance company for the vaccine, your co-payment or out-of-pocket is determined by your plan’s benefits. If you do not have insurance, you will be responsible for the $45 administration of the vaccine and St. Luke's will bill you.
Yes, the CDC has updated their guidance to state that health workers may administer another needed vaccine at the same time as the COVID vaccine. This applies to patients of any age.
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The CDC has published information on What to Expect after Getting a COVID-19 Vaccine and posts updates as more information becomes available.
The Centers for Disease Control recommends COVID-19 boosters after the primary series for those 12 and older who received the Pfizer or Moderna vaccine for their initial series six or more months ago or who received Johnson & Johnson two or more months ago. Recently, the FDA and CDC approved bivalent mRNA COVID-19 vaccines for boosters for ages 5 and older, and the monovalent vaccines were no longer authorized under emergency use authorization for use as boosters in these age groups. A single booster dose with an updated bivalent COVID-19 vaccine is designed to provide broad protection against COVID-19 and better protection against COVID-19 caused by the currently circulating Omicron variants, BA.4 and BA.5. Those who received the monovalent booster recently should wait at least eight weeks before receiving the bivalent booster.
Appointments should be scheduled through MyChart or by calling (208) 381-9500.
While you may prefer to receive the same brand COVID-19 vaccine for your primary series and booster, federal agencies have approved a “mix-and-match” approach with vaccination products where necessary or sought by patients. We can accommodate this CDC guideline at our clinics and vaccination sites.
When you receive a vaccination in one of our clinics, you will have the option to be monitored for about 15 minutes and medical staff will use safety precautions and respond immediately if you have an initial reaction. If you have a delayed reaction, please contact your primary care provider or call 911.
It is most safe to visit those who are also vaccinated. The COVID-19 vaccines are not 100% effective and some, such as those who are unable to be vaccinated (e.g., young children) and some immunocompromised people who may not have developed robust antibodies to the vaccine, may be less protected and/or not protected.
Getting the COVID-19 vaccine will affect when or if you are eligible to donate blood. View Red Cross guidelines