Global Statistics

All countries
554,450,929
Confirmed
Updated on July 4, 2022 7:56 am
All countries
526,775,539
Recovered
Updated on July 4, 2022 7:56 am
All countries
6,361,548
Deaths
Updated on July 4, 2022 7:56 am

Global Statistics

All countries
554,450,929
Confirmed
Updated on July 4, 2022 7:56 am
All countries
526,775,539
Recovered
Updated on July 4, 2022 7:56 am
All countries
6,361,548
Deaths
Updated on July 4, 2022 7:56 am
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Can You Be On Antibiotics And Get Covid Vaccine

What Is A Common Vaccine Reaction

Can I get the COVID-19 vaccine if Im on an antibiotic?

According to the NHS, the most common side effects of vaccination are:

  • the area where the needle goes in looking red, swollen and feeling a bit sore for 2 to 3 days
  • babies or young children feeling a bit unwell or developing a;high temperature;for 1 or 2 days

It’s “rare” for anyone to have a serious allergic reaction to a vaccination, the NHS says.

If this does happen, it usually happens within minutes.

The person who vaccinates you or your child will be trained to deal with allergic reactions and treat them immediately. With prompt treatment, you will make a good recovery.

The Pfizer/BioNTech jab showed the following side effects in trials:

Like all vaccines, the new coronavirus vaccine can cause side effects, although not everybody gets them.

Very common;

  • Pain at injection site

Uncommon;;

  • Enlarged lymph nodes
  • Feeling unwell

The NHS says all vaccines are thoroughly tested to make sure they will not harm you or your child.

It often takes many years for a vaccine to make it through the trials and tests it needs to pass for approval.

But scientists have been working at speed to develop a Covid jab in under one year.

This has been possible because of huge funding, global collaboration, and because there was high transmission of the virus globally to test it.

Experts have said “no corners have been cut” in testing Covid vaccines.

Once a vaccine is being used in the UK it’s also monitored for any rare side effects by the Medicines and Healthcare products Regulatory Agency .

We Don’t Talk About Herd Immunity For Protection Against Influenza Or Other Common Viral Infections So Why Is It Discussed So Much With Covid

Herd immunity is a concept used in public health to describe a situation in which the more people in a community immune to a particular pathogen, the fewer people available for that pathogen to infect. As the infectious agent spreads through a community, it has more trouble finding susceptible people if most of those around them are immune. In this manner, we rely on herd immunity for viruses, such as measles, rubella, polio, and chickenpox, among others, even if we are not having conversations about it. Influenza is more difficult because the virus changes so much from one year to the next and as such, vaccination does not offer long-term protection.

Related to COVID-19, herd immunity has been discussed more frequently for a couple of reasons. First, because this is a completely new virus, no one had pre-existing immunity. People can become immune to SARS-Co-V2, the virus that causes COVID-19, in two ways through disease or through vaccination. By monitoring how many people are immune relative to the entire population, public health officials can offer informed guidance related to easing restrictions meant to stem spread of the virus.

Herd immunity can only be induced by vaccination. Never in history has any virus infection been eliminated because of immunity induced by natural infection.

Q: Will Miracle Mineral Solution Cure Covid

A: ;No. Miracle Mineral Solution does not cure COVID-19 and has not been approved by the FDA for any use. The solution, when mixed as directed, forms industrial bleach that may cause serious and potentially life-threatening side effects. FDA took action against Genesis II Church of Health and Healing for unlawfully distributing Miracle Mineral Solution for the treatment of COVID-19 and other diseases. Learn more: Danger: Dont Drink Miracle Mineral Solution or Similar Products.;

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At The Current Rate Of Rollout How Long Will It Take Before Iowa Reaches Herd Immunity Against Covid

About 75 percent of the population needs to be vaccinated it can reach herd immunity. Based on the state’s current rollout, Winokur believes it will be summer or fall before Iowa reaches that immunity.

New vaccines, in addition to the ones developed by Pfizer and Moderna, will likely be considered in the near future by federal officials. These include shots developed by Johnson & Johnson and AstraZeneca.

The University of Iowa Hospitals and Clinics is also participating in a clinical trial for a new vaccine developed by Novavax.

Winokur said the trial still is in the midst of recruiting 30,000 participants, and researchers will need to wait at least a month after half of the participants have received the second dose before seeking federal emergency use authorization. She estimated it will be at least until March until that occurs.

When asked whether Iowans outside of Iowa City could participate in the clinical trial, UIHC officials said they ‘do not have the infrastructure and manpower to send our team to distant locations at this time.

‘All personnel working on the study have to be specifically trained for performing clinical research in general and have to be trained for this particular protocol, officials said in a statement. ‘What often isn’t obvious is that we have a large team of individuals working behind the scenes for every single study visit, and these visits will be ongoing for two years.

Q: What Is The Fda Doing To Respond To The Covid

Vaccines Give You the Coronavirus that the Government Can ...

A: The FDA, along with other federal, state, and local agencies and public health officials across the country and internationally, plays a critical role in protecting public health during the COVID-19 pandemic. FDA staff are working around the clock to support development of ;medical countermeasures and are providing regulatory advice, guidance, and technical assistance to advance the development and availability of vaccines, therapies, diagnostic tests and other medical devices for use diagnosing, treating, and preventing this novel virus. The FDA continues to monitor the human and animal food supply and take swift action on fraudulent COVID-19 products.

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Does A Vaccinated Person Present A Risk To Unvaccinated Family Members In The Same House

Vaccinated people do not shed virus as a result of vaccination. Neither the mRNA nor the adenovirus vaccines are composed of live viruses, so there is no infectious virus to spread from a vaccinated person to someone else.

But we do not yet know if a vaccinated person who encounters the virus can still experience what is referred to as asymptomatic infection. An asymptomatic infection occurs when a person is exposed to the virus in the community and the virus can still replicate in their body, but they dont have symptoms because their immune system stifles the infection as a result of vaccination. In this scenario, the person could potentially spread the virus without even knowing they are infected. While it is not anticipated that vaccinated individuals will be likely to spread the virus even if they experience asymptomatic infection, this has not yet been shown to be the case. Therefore, we need to practice caution until we know for certain.

Given that families and friends will not all be vaccinated yet, vaccinated individuals should continue to follow public health guidance when they are out in the community to decrease the chance of introducing the virus in the home through asymptomatic infection. Likewise, even when a whole family is vaccinated, continuing to practice these measures will be important for two reasons:1. The vaccine will not work for everyone, so someone in the home who has been vaccinated may still be susceptible.

How Long Before A Coronavirus Vaccine Takes Effect

The mRNA vaccines require two doses. While people will have some immunity after the first dose, protection will be most likely about one week after receipt of the second dose.

The adenovirus vaccine requires one dose. While people will have some immunity about two weeks after being vaccinated, protection will be more robust about one month after receipt of the vaccine.

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Q: What Do I Need To Know About The Temporary Policy For Food Labeling Of Minor Ingredient Changes During The Covid

A:;Although the temporary policy allows some flexibility, the eight major food allergens under the Food Allergen Labeling and Consumer Protection Act of 2004 cannot be substituted for labeled ingredients by manufacturers without a corresponding label change. While the temporary policy does not list all ingredients known to cause sensitivities in some people, manufacturers should avoid substituting ingredients with major food allergens or with ingredients recognized as priority allergens in other parts of the world without a label change. These flexibilities are intended to remain in effect only for the duration of the COVID-19 public health emergency in the United States. However, when this public health emergency is over, extensions may be needed if the food and agriculture sectors need additional time to bring supply chains back into regular order. For more information please see more Questions and Answers on FDAs Temporary Policy on Food Labeling Changes During the COVID-19 Pandemic.

Is It Safe To Have The Covid

Will the COVID-19 vaccine interfere with my antibiotics or medications? | KVUE

Yes, it is safe.

The COVID-19 vaccine helps your bodys immune system to identify the coronavirus, which enables you to fight it off more quickly and effectively. The vaccine essentially trains your immune cells to identify, attack and kill the virus.

Antibiotics, on the other hand, kill the bacteria that are causing an infection in your body. This means that your antibiotics should have no impact on the coronavirus or the vaccine, and the vaccine should have no impact on your bacterial infection or your antibiotics.

If you have any immediate medical concerns about your health or your treatment, please contact your GP or healthcare provider. If you would like support and information related to an antibiotic-resistant infection, you can reach out to our Patient Support Service who will be happy to listen and help.

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Q: Are There Any Approved Products That Can Prevent Or Treat Covid

A: No. Under the Federal Food, Drug, and Cosmetic Act, articles intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in man or other animals are drugs. The FDA has not approved any drugs for the diagnosis, cure, mitigation, treatment, or prevention of COVID-19 in animals.;The U.S. Department of Agricultures Animal and Plant Health Inspection Service Center for Veterinary Biologics regulates veterinary biologics, including vaccines, diagnostic kits, and other products of biological origin. Similarly, APHIS CVB has not licensed any products to treat or prevent COVID-19 in animals.

The FDA has taken action against unapproved products claiming to prevent or cure COVID-19. The public can help safeguard human and animal health by reporting any products claiming to do so to or 1-888-INFO-FDA .

Should I Get A Vaccine If I’m Immunocompromised

Federal officials say people who have an impaired immune system, including those on immunosuppressant medication, can still receive the vaccine.

The vaccine is just as safe for people who are immunocompromised as it is for others, but the efficacy might be lower, Winokur said.

‘But we do recommend they get vaccinated, she said.

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The Importance Of Getting The Covid

The criteria for people who should not get a COVID-19 vaccine is very narrow. The CDC is saying that people who have had a severe allergic reaction to a previous dose of a COVID-19 vaccine should not receive another dose, for now .

But for everyone else including people who had non-anaphylactic allergic reactions to a COVID-19 vaccine, people who have allergies to ingredients in the COVID-19 vaccine, and people who have had allergic reactions to infused or injectable medications the vaccine may be given, but its important to discuss this with your doctor and make sure the vaccine can be given in a safe environment. This means making sure the person can be observed for 30 minutes afterward and medical care is available.

It may seem concerning that some people have had allergic reactions to the vaccine, but keep in mind that the number of reactions is very small in comparison to the total amount of vaccines administered.

And most important: The overall statement that people should be aware of is that the benefits of getting the COVID-19 vaccine far outweigh the risks of the possible chance of an anaphylactic reaction to the vaccine, says Dr. Kreiner.

If youre worried about potential allergic reactions to the COVID-19 vaccine, the best course of action is to speak to your doctor about any previous allergic reactions youve had.

Your physician can then compare what youve had prior reactions to with the list of ingredients in the vaccines.

What Do You Know About The Halt On The J&j Vaccine

A COVID

Federal health officials recommended a pause on the Johnson & Johnson COVID-19 vaccine after six women developed blood clots in their brain up to 3 weeks after their vaccine. The blood clots in the brain are called cerebral venous sinus thrombosis . While a few of these women had an underlying health condition, no pattern of pre-existing conditions emerged. These cases are similar to those caused in European countries by the AstraZeneca vaccine, which is not currently used in the United States. The J&J and AZ vaccines are similar in that both use an adenovirus vector to induce immunity to the SARS-C0V-2 surface protein, but they use different adenovirus vectors. The J&J vaccine uses a human adenovirus, and the AZ version uses a chimp adenovirus.

The pause was recommended for three reasons:

  • First, the FDA and CDC needed time to review these cases and collect as much information as they could to figure out what was happening.
  • Second, they needed to update healthcare providers across the country on what to watch for in their patients. In this way, physicians can properly diagnose and treat the condition. This condition is very rare and treating it with blood thinners could make this situation worse.
  • Third, the pause allowed for the public to quickly become aware of the potential side effect, so that people who got the vaccine and those around them would be more likely to recognize the need to seek medical attention if they experience symptoms.

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If I Dont Have Side Effects Does That Mean The Vaccine Did Not Work

Many people will get the vaccine and not experience side effects. This does not mean that the vaccine did not work for them. In the clinical trials side effects occurred at varying rates, for example only about 1 to 20 of every 100 people who received the mRNA vaccine had a fever, but we know that the mRNA vaccine worked for more than 90 of every 100 people.

Antibiotics And The Covid

Gemma King Coronavirus COVID-19

More people are receiving one of the newly developed COVID-19 vaccines every day. However, Antibiotic Research UKs Patient Support Service is seeing an increasing number of queries from people who are concerned about having the vaccine while they are also taking antibiotics.

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Children Cannot Get Vaccinated

Those 16 and under cannot get a vaccine at this time. “I don’t think we’re going to see it in the first half of this coming year,” Dr. Jose Romero, the chair of the CDC’s Advisory Committee for Immunization Practices, said during an interview on MSNBC. “We need to see how the studies progress. We need to see that data in order to make sure that it is safe and effective in children.” So get vaccinated when it becomes available to youand to ensure your health and the health of others, don’t miss these;Signs Your Illness is Actually Coronavirus in Disguise.

Eat This, Not That!

If I Have An Autoimmune Or Immune

Can you cross state lines to get the COVID-19 vaccine?

People with immune-compromising conditions may get the COVID-19 vaccine as long as they are not in one of the following categories:

  • Severe allergy to a vaccine component
  • History of severe allergy to any vaccine or injectable medication

However, it is recommended that individuals with compromised immune systems discuss their personal risks and benefits with a healthcare provider to determine whether to receive the vaccine. Data about how well the vaccine works and its safety in immune-compromised individuals are not currently available, so it is possible that these individuals could have a lower immune response to vaccination. On the other hand, persons with these conditions may also be at higher risk of severe disease due to COVID-19. Therefore, the CDC recommended that people who are immune-compromised or taking immunosuppressive medications could receive the vaccine if they wanted as long as they do not have other contraindications.

With this said, knowing the potential for a lower immune response, if someone with an immune-compromising condition decides to get vaccinated, it will be important to get both doses; and practice other public health measures until more is known about their protection against SARS-CoV-2, the virus that causes COVID-19.Post-licensure monitoring systems, like the Vaccine Adverse Events Reporting System and the Vaccine Safety Datalink , will be used to allow; for real-time monitoring of these sub-groups.

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Q: What Is An Emergency Use Authorization And How Is It Being Used To Respond To Covid

A: In certain types of emergencies, the FDA can issue an emergency use authorization, or EUA, to provide more timely access to critical medical products that may help during the emergency when there are no adequate, approved, and available alternative options.

The EUA process is different than FDA approval, clearance, or licensing because the EUA standard may permit authorization based on significantly less data than would be required for approval, clearance, or licensing by the FDA. This enables the FDA to authorize the emergency use of medical products that meet the criteria within weeks rather than months to years.;

EUAs are in effect until the emergency declaration ends but can be revised or revoked as we evaluate the needs during the emergency and new data on the products safety and effectiveness, or as products meet the criteria to become approved, cleared, or licensed by the FDA.

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