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Learn

AstraZeneca’s COVID-19 vaccine (AZD1222) was co-invented with the University of Oxford is in Phase 3 trials in the United States and has been approved for use in the United Kingdom.

Find the AstraZeneca COVID-19 vaccine information here.

Read more

Sanofi and GlaxoSmithKline have joined forces to start developing a COVID-19 vaccine and is tracking much later than other companies with phase 1/2 testing starting in early September and no efficacy data has been released so far.

Find the Sanofi and GSK COVID-19 vaccine information here.

Read more

Merck started developing its COVID-19 vaccine (V590) much later than other companies with phase 1/2 testing starting in early September and no efficacy data has been released so far.

Find the Merck COVID-19 vaccine information here.

Read more

Find the Novavax COVID-19 vaccine Information here.

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The Janssen: Pharmaceutical Companies of Johnson & Johnson COVID-19 vaccine has been approved for Emergency Use Authorization by the FDA and will start rolling out in the United States as a Single Dose Covid-19 vaccine.

Find the Johnson & Johnson COVID-19 vaccine information here.

Read more

 

Moderna’s COVID-19 vaccine (mRNA-1273) finished Phase 3 and is approved for Emergency Use Authorization by FDA and is one of the two major vaccines being distributed in the United States and around the world.

Find the Moderna COVID-19 vaccine information here.

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Pfizer has developed a COVID-19 vaccine, BNT162b2, along with and BioNTech SE that has concluded Phase 3 trials and has shown an efficacy rate of 95% in participants without prior SARS-CoV-2 infection. The vaccine is approved for use under the Emergency Use Authorization from the FDA.

Find the Pfizer COVID-19 vaccine information here.

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Recent Interesting Reports

April 29, 2021 10:25 AM

““I purchased this Stihl chain saw on Feb 4, 2021 from Blackcass but to date all I received was a chain with grips. I would like my saw as ordered or a full refund and they pay for shipping. See Less
Reported By SafelyHQ.com User

April 12, 2021 1:00 PM

“Company name: J. M. Smucker Co.
Brand name: Meow Mix®
Product recalled: Meow Mix® Original Choice Dry Cat Food
Reason of the recall: Potential Salmonella Contamination
FDA Recall date: April 12, 2021
Recall details: Orrville, OH – The J. M. Smucker Co. today announced a limited, voluntary recal... See Morel of two lots of Meow Mix® Original Choice Dry Cat Food (30LB bag) due to potential salmonella contamination. The Company has received no reports of pet illness or adverse reaction and has issued this recall out of an abundance of caution.

The impacted products were sold at select Walmart stores in IL, MO, NE, NM, OK, UT, WI, and WY. No other Meow Mix® products are impacted by this recall. If pet parents have products matching the following description in their possession, they should stop feeding it to their cats and dispose of it immediately. This information can be found on the bottom and back of each bag.

- Meow Mix® Original Choice Dry Cat Food (30 LB Bag). Retail UPC Code: 2927452099. Lot Code: 1081804. Best If Used By Date: 9/14/2022
- Meow Mix® Original Choice Dry Cat Food (30 LB Bag). Retail UPC Code: 2927452099. Lot Code: 1082804. Best If Used By Date: 9/15/2022

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Pfizer BioNTech vaccine, Walgreens, Ohio 43, Streetsboro, OH, USA

Symptoms: Fatigue Lightheaded Muscle Pain Soreness
Walgreens, Ohio 43, Streetsboro, OH, USA

April 28, 2021 5:52 PM

“Got the first dose of the Pfizer vaccine yesterday at Walgreens. Process was very smooth, no allergic reactions. Had some initial wooziness and lightheadedness 5 minutes after receiving the vaccine but may have just been anxiety.

Symptoms after 27 hours: sore arm, joint and muscle pain, fatigue.... See MoreFeeling warm/flushed but no fever. See Less
Reported By SafelyHQ.com User

May 6, 2021 12:47 AM

“This was all after waiting the 20 minutes before leaving within 5 minutes after getting in my car I felt a burning in my right foot that within 20 minutes was burning both feet and legs all the way. Burning in my body from the waste down for 4 hours then severe rash all over my body except my face. See Less
Reported By SafelyHQ.com User

April 30, 2021 3:56 PM

“The same still saw scam as the other people on here. Same ad. It states $19.99 for that day and I ordered it. I also got the little manual wire saw. It said saw and accessories. It really hurts people on a fixed income. I hope they are proud of themselve See Less
Reported By SafelyHQ.com User

April 22, 2021 10:09 AM

“Yes. I also ordered the GTA 26 battery-powered electric chainsaw. I got the chain with handles. I was bantering back and forth with Chinese agent, who really does not know what to do except to try and get more money from me for an inferior chainsaw for $6. I ordered a GTA 26 chainsaw, Stihl brand. I... See Moregot the hand chainsaw (had never heard of using a chain by hand, but it is an actual thing). I don't think you can convert the hand chainsaw to using it with an actual chain saw anyway. The Chinese agent is trying appease me by saying I can get a chainsaw to use with the chain for $60. The website he sent me show a completely different chainsaw for 29.99 and he sent the actual picture of the See Less
Reported By SafelyHQ.com User

May 4, 2021 9:01 PM

“Company name: Hospira, Inc.
Brand name: Hospira, Inc.
Product recalled: 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and 1% Lidocaine HCl Injection, USP 30 mL
Reason of the recall: Due to mislabeling
FDA Recall date: May 04, 2021
Recall details: Hospira, Inc., a Pfizer company, is volun... See Moretarily recalling lot EG6023 of 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and lot EG8933 of 1% Lidocaine HCl Injection, USP 30 mL, to the hospital/institution level due to mislabeling whereby a portion of each lot was incorrectly labeled as the other product. This issue was identified as part of the investigation of a confirmed customer report.

Hospira’s assessment of the potential risk to patients concluded that the use of the impacted product is likely to cause adverse events of moderate to high severity. If 1% lidocaine is administered to the patient instead of 0.5% bupivacaine, the patient may be underdosed, leading to lack of efficacy with potential outcomes such as inadequate pain management, and failure of surgical anesthesia. If 0.5% bupivacaine is administered to the patient instead of 1% lidocaine, an overdose of bupivacaine may occur, which could lead to potential outcomes such as seizures; respiratory abnormalities including low oxygen and/or elevated carbon dioxide in the blood, too much acid in the body fluids, and temporary cessation of breathing; heart abnormalities such as heart contraction and/or relaxation issues, irregular heartbeat, slower than normal heart rate, abnormal heart rhythm in which the ventricles of the heart quiver instead of pumping normally, cardiac arrest and cardiac flatline.

To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for these lots. 0.5% Bupivacaine Hydrochloride Injection, USP is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and obstetrical procedures. 1% Lidocaine HCl Injection, USP is indicated for the production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks when the accepted procedures for these techniques as described in standard textbooks are observed.

The NDC, Lot Number, Expiration Date, Strength and Configuration details for 0.5% Bupivacaine Hydrochloride Injection, USP and 1% Lidocaine HCl Injection, USP are in the table below and a photo of the products can be found at the end of this press release. The product lots were distributed nationwide to wholesalers, distributors, retailers, and hospitals in the United States, Puerto Rico and Guam from December 29, 2020 to April 15, 2021.

- 0.5% Bupivacaine Hydrochloride Injection, USP, Single Dose Teartop Vial. NDC: Vial: 0409-1162-19 Tray: 0409-1162-02. Lot number: EG6023. Expiration Date: 01 July 2022. Strength: 0.5%, 150 mg/30 mL (5 mg/mL). Configuration/ Count: Case Pack 2 x 25 Vials.
- 1% Lidocaine HCl Injection, USP Single Dose Teartop Vial. NDC: Vial: 0409-4279-16 Tray: 0409-4279-02. Lot number: EG8933. Expiration Date: 01 Aug 2022. Strength: 1%, 300 mg/30 mL (10 mg/mL). Configuration/ Count: Case Pack 2 x 25 Vials.

Hospira, Inc., places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Hospira, Inc. has notified wholesalers, distributors, retailers, and hospitals by mail to arrange for return of any recalled product.

Wholesalers, distributors or retailers with an existing inventory of the lot, which is being recalled, should stop administration and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or retail level, please notify any accounts or additional locations which may have received the recalled product from you.

Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall. For additional assistance, call Stericycle at 1-800-805-3093 between the hours of 8 a.m. to 5 p.m. ET, Monday through Friday.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Petmatrix Dreambone Dino Chews, Yulee, FL, USA

Symptoms: Vomiting Other
Yulee, FL, USA

April 27, 2021 9:13 AM

“We gave our dog the Dreambone Dino Chews on Sunday. On Tuesday we noticed he was wanting to go into his kennel and sleep. Tuesday evening he was acting odd with jerking movement, sticking his tongue out, oddly staring at the ceiling and refusing to drink water. We immediately took him to the vet whe... See Morere they induced vomiting, gave him antibiotics and an IV. He continued to not drink water in his own and show neurological behaviors that our vet said was focal seizures, lip-licking and star-gazing. The Dreambone treats were the only change in his diet. He would not drink water on his own for at least 3 days and he had focal seizures on and off for about 5 days. Do not give your dog any Petmatrix, Spectrum, or Dreambone product. They will poison your beloved pet. They package says they are made in China and when you google the company they are also made in Vietnam. See Less
Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Doctor visit

April 18, 2021 10:04 AM

“I have 2 sick, A week and a half ago Née bag of Kibbles and bits bistro and the Melody Just started about a week and a half ago now I have two dogs sick one with an IV in the hospital See Less
Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Hospital

April 21, 2021 12:38 PM

“Blackcass.com is a total scam. My wife bought me what she thought was a mini electric chain saw. The site showed a sthil chain saw for $29.99 instead of $59.99. Not knowing the prices on tools she thought to surprise me. The next day I found her order in our computer and immediately contacted them a... See Morend tried to cancel it. They said it was too late as the order had already been processed. 10 weeks later we got a hand rose clipper instead. My wife had paid $37.99 for a clipper I got at Ace hardware before for $9.99 See Less
Reported By SafelyHQ.com User