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There are currently 7 leading Covid-19 vaccines from major pharmaceutical companies in different stages of development. The vaccines use different mechanisms of action and all have some form of side effects ranging from mild to severe with common side effects including fever, headaches, muscle pain, and injection site reactions.
Here is a brief summary of each COVID-19 vaccine:
Pfizer COVID-19 vaccine -
Pfizer developed its COVID-19 mRNA 2 dose vaccine along with BioNTech and has shown an efficacy rate of 95% in clinical trials. It is close to being approved or has been approved for use in the UK, Europe, and the US. It is now being distributed in the UK and will be distributed in the US by the end of 2020. Major side effects are beginning to be reported from the UK vaccine recipients.
For more information about the Pfizer COVID-19 vaccine click here
Moderna COVID-19 vaccine -
Moderna’s 2 dose mRNA COVID-19 vaccine (mRNA-1273) is currently finishing Phase 3 trials and has shown a vaccine efficacy of 94.5%. The Moderna vaccine has shown mild to moderate side effects including chills, fevers, headache, shortness of breath, pain in the arm.
For more information about the Moderna COVID-19 vaccine click here
AstraZeneca COVID-19 vaccine -
AstraZeneca’s 2 doses COVID-19 vaccine was co-invented with the University of Oxford is in Phase 3 trials and has shown that it has an average efficacy of 70%. The vaccine uses a weakened version of a related virus with elements of the new virus carried along. The vaccine has shown side effects including fever, headaches, muscle pain, and injection site reactions, and all were deemed mild or moderate.
For more information about the AstraZeneca COVID-19 vaccine click here
Johnson & Johnson COVID-19 vaccine -
Janssen: Pharmaceutical Companies of Johnson & Johnson's COVID-19 vaccine is currently in Phase 3 trials and is being tested as a single dose and two-dose regimens. The Johnson & Johnson COVID-19 vaccine is based on using a weakened version of a common cold virus with elements of the new virus carried along. The vaccine has induced local and systemic side-effects that are mild, to moderate and the trial was briefly paused after an experienced unexplained illness.
For more information about the Johnson & Johnson COVID-19 vaccine click here
Novavax COVID-19 vaccine -
Novavax’s 2 dose COVID-19 vaccine is currently starting phase 3 clinical trials and the FDA has granted the vaccine Fast Track Designation. The Novavax COVID-19 vaccine uses protein subunit vaccine technology to an immune response. Side effects ranged from mild to severe and included pain at the site of injection, headaches, muscle pain, and fatigue.
For more information about the Novavax COVID-19 vaccine click here
Merck COVID-19 vaccine –
Merck's COVID-19 vaccine started clinical trials in early September. The vaccine is being tested to be given orally in a single dose. The Merck COVID-19 vaccine is based on using a weakened version of a related virus with elements of the new virus carried along. The vaccine has just started clinical trials, so no side effects have been uncovered yet.
For more information about the Merck COVID-19 vaccine click here
Sanofi and GSK COVID-19 vaccine -
The Sanofi and GlaxoSmithKline COVID-19 vaccine started an early phase clinical trial in early September. The vaccine is a two-dose recombinant protein vaccine with an adjuvant. With clinical trials just beginning for the Sanofi and GSK COVID-19 vaccine the side effects are still to be uncovered. Sanofi and GSK have also signed a deal with the Canadian government for 200 million doses.
For more information about the Sanofi + GSK COVID-19 vaccine click here
Recent Interesting Reports
3 weeks ago
Plastikon Healthcare, LLC is voluntarily recalling one (1) lot of Milk of Magnesia 2400 mg/10 mL Oral Suspension, one (1) lot of Milk of Magnesia 2400 mg/30 mL Oral Suspension, eleven (11) lots of Magnesium Hydroxide 1200 mg/Aluminum Hydroxide 1200 mg/Simethicone 120 mg per 30 mL Oral... Suspension, and two (2) lots of Magnesium Hydroxide 2400 mg/Aluminum Hydroxide 2400 mg/Simethicone 240 mg per 30 mL Oral Suspension to the consumer level. The products are being recalled due to microbial contamination. To date, Plastikon Healthcare has not received any reports of adverse events or injuries related to this recall.
Risk Statement: Administration or use of oral drug products with microbial contamination could potentially result in increased infections that may require medical intervention. Patients with compromised immune systems, such as patients in hospitals and nursing homes, have a higher probability of developing potentially life-threatening infections after taking a contaminated product.
Product indication, lot numbers, expiration dates, and NDC information are listed in the link below. The products are packaged for institutional use and are sold to clinics and hospitals nationwide in single use cups with a foil lid. The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 7/1/2020 and 10/31/2021, who shipped to hospitals, nursing homes, and clinics nationwide. The products are private labeled for Major Pharmaceuticals.
Plastikon Healthcare is notifying its direct customers via a recall letter to arrange for return of any recalled product. Anyone with an existing inventory of the lots which are being recalled should stop use and distribution, and quarantine immediately. Return all quarantined product to the place of purchase. For clinics, hospitals, or healthcare providers that have dispensed product to patients, please notify patients regarding the recall.
Consumers with questions regarding this recall can contact Plastikon Healthcare by phone at (785) 330-7109 Monday through Friday from 9 am to 4 pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Company name: Plastikon Healthcare, LLC
Brand name: Plastikon Healthcare, LLC
Product recalled: Milk of Magnesia, Magnisium Hydroxide/Aluminum Hydroxide/Simethicone Oral Suspension
Reason of the recall: Due to microbial contamination
FDA Recall date: June 08, 2022
2 weeks ago
We had a chorgy mix about 4 ibs that started not eating or drinking. Didn't want to move and basically died within 2 days . Was vomiting and diarrhea also. Going to have dog food tested. Will be following back. Dogs have been eating this food for at least 3 years.
1 week ago
as I stated before, I just opened a brand new bag of Dreambones and saw that there is black mold on the bones
6/6/2022, at 2323:43 to be more precise. A significant and extensive sonic boom tore through our house, woke us, terrified our dogs and causes creaking that continued for several more seconds. It is not the “sound of freedom.” It is poor and unaware flying. It is also... profoundly disturbing especially in these crazy times. Our dogs didn’t settle for an hour. I didn’t settle until almost 3 am. This can’t be allowed by city ordinance. Extremely disruptive. I do have it on our doorbell and on inside house camera. It was so loud, it tripped the recordings.
4 days ago
Pony Green (shenlantiaodong) I usually buy something on the Internet since furtanamente I fell into a scam and they don't give me a solution and they told me that this company doesn't even exist and they grab deceptive sales nothing to do with what they are selling, in fact I don't sign and don't receive anything they're selling it with
There are several trees at Pinch Pond family campground that are either half or completely dead. I am concerned that with a strong storm a tree is going to fall on a camper or worse have someone in it!
The CDC announced that they are currently investigating multistate outbreaks of Salmonella infections with serotypes Enteritidis, Hadar, Infantis, and Typhimurium.
As of June 2, 2022, 219 people infected with one of the outbreak strains have been reported from 38 states. 27 have been hospitalized. One death has... been reported from Tennessee. Illnesses started on dates ranging from February 15, 2022, to May 19, 2022.
State and local public health officials are interviewing people about the animals they came into contact with in the week before they got sick. Of the 87 people interviewed, 61 (70%) reported contact with backyard poultry before getting sick. Of 56 people with information available, 16 reported eating eggs from backyard poultry, and 2 reported eating meat from backyard poultry.
Backyard poultry, like chickens and ducks, can carry Salmonella germs even if they look healthy and clean. These germs can easily spread to anything in the areas where the poultry live and roam. You can get sick from touching your backyard poultry or anything in their environment and then touching your mouth or food and swallowing Salmonella germs.
CDC advises Backyard Flock Owners:
-Always wash your hands with soap and water immediately after touching backyard poultry, their eggs, or anything in the area where they live and roam.
- Use hand sanitizer if soap and water are not readily available. Consider having hand sanitizer at your coop.
- Don’t kiss or snuggle backyard poultry, and don’t eat or drink around them. This can spread Salmonella germs to your mouth and make you sick.
- Keep your backyard flock and supplies you use to care for them (like feed containers and shoes you wear in the coop) outside of the house. You should also clean the supplies outside the house.
-Don’t let children younger than 5 years touch chicks, ducklings, or other backyard poultry. Young children are more likely to get sick from germs like Salmonella.
- Collect eggs often. Eggs that sit in the nest can become dirty or break.
- Throw away cracked eggs. Germs on the shell can more easily enter the egg through a cracked shell.
- Rub off dirt on eggs with fine sandpaper, a brush, or a cloth. Don’t wash eggs because colder water can pull germs into the egg.
- Refrigerate eggs to keep them fresh and slow the growth of germs.
- Cook eggs until both the yolk and white are firm, and cook egg dishes to an internal temperature of 160°F to kill all germs.
In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Hauppauge, NY, Loud Muscle Science, LLC is voluntarily recalling the following Launch Sequence products and lots listed in the table below to the consumer level. Laboratory analysis undertaken at the request of Loud Muscle Science, LLC found the products to be tainted with tadalafil, an ingredient in... FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The presence of tadalafil in the Launch Sequence products makes these products unapproved drugs for which the safety and efficacy have not been established and therefore, subject to recall.
Risk Statement: The most critical potential adverse health consequence of unintentional consumption of a product tainted with undeclared tadalafil is profound, life-threatening hypotension related to drug-drug interactions with nitroglycerin or guanylate cyclase inhibitors.
In the expected-use population, profound hypotension can result in a heart attack, stroke or death. To date, Loud Muscle Science has not received any reports of adverse events related to this recall. These tainted Launch Sequence Capsule products are marketed as dietary supplements for male sexual enhancement. The affected products are:
- Launch Sequence Capsules. Package Size: 60. (Bottle) ASIN: B07TLPWXDS. UPC Code: 641378938375.
- Launch Sequence Euphoria Capsules. Package Size: 10. (Tin) ASIN: B08ZJX4V9J. UPC Code: 661020846864.
- Launch Sequence Aphrodisia Capsules. Package Size: 4. (Tin) ASIN: B07QB3S2LV. UPC Code: 661020846957.
- Launch Sequence Capsules. Package Size: 60. (Bottle) ASIN: B08HM7VHCX. UPC Code: 661020848166.
- Launch Sequence Euphoria Capsules. Package Size: 10. (Tin) ASIN: B08ZJX4V9J. UPC Code: 661020846864.
- Launch Sequence Aphrodisia Capsules. Package Size: 4. (Tin) ASIN: B09S12VK3F. UPC Code: 661020846957.
The full list of lots and expiry dates is available at the link below. The Launce Sequence capsule products were sold under Amazon ASIN Nos. B07TLPWXDS (USA 60 count) and B08HM7VHCX (Canada 60 count); Launch Sequence Euphoria capsule products were sold under Amazon ASIN Nos. B08ZJX4V9J (Euphoria USA 10 count) and B08ZJX4V9J (Euphoria Canada 10 count); and Launch Sequence Aphrodisia capsule products were sold under Amazon ASIN Nos. B07QB3S2LV (Aphrodisia USA 4 count) and B09S12VK3F (Aphrodisia Canada 4 count).
The products can be identified by the labels and packaging below. The product was marketed via the Internet and fulfilled by Amazon at www.amazon.com Nationwide in the USA and www.amazon.ca in Canada, on eBay.com, and in retail stores.
Loud Muscle Science is notifying its distributors and customers by letter and this press announcement and providing a refund to its customers. Consumers that have the Launch Sequence products should stop using the product and discard.
Consumers with questions regarding this recall can contact Loud Muscle Science, LLC by phone number: 631-270-4188 -- Monday through Friday 9AM – 4PM EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Company name: Loud Muscle Science, LLC
Brand name: Launch Sequence
Product recalled: Launch Sequence Aphrodisia and Euphoria Capsules
Reason of the recall: Contain Tadalafil
FDA Recall date: June 30, 2022