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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Goodbye! and best wishes in your recovery

JJ vaccine side effects , San Jose, CA, USA

April 9, 2021 6:03 PM

San Jose, California, United States

Symptoms: Fever Headache Chest Pain Fatigue

Got JJ vaccine and after about 2 hrs got severe palpitations and fever abt 101, started heavy anxiety and breathing difficulties. Next day fever reduced with tylenol then had headache and chest pain. Visited urgent care and my ekg was normal. It’s been a week still feel very tired and low energy, although no fever or headache or chest pain

Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Urgent Care

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Recent Interesting Reports

May 10, 2021 4:00 PM

“Company name: Novo Nordisk
Brand name: Levemir, Tresiba, Fiasp, Novolog and Xultophy
Product recalled: Product Samples
Reason of the recall: Due to improper storage temperature conditions
FDA Recall date: May 10, 2021
Recall details: Novo Nordisk is voluntarily recalling 1,468 product samples... See Morelisted in the table below of Levemir®, Tresiba®, Fiasp®, Novolog® and Xultophy®, to the consumer level. These products are being recalled because they were stored at temperatures below storage requirements.

This recall only impacts product samples and does not impact product that has been broadly distributed to pharmacies or mail-order services. If product samples are exposed to temperatures below 32°F, it could cause a lack of efficacy and damage to the cartridge and pen-injectors. If product from an improperly stored vial, cartridge or pen-injector is used, there is a risk that you might not receive the right amount of medicine as intended which may lead to hyperglycemia or hypoglycemia resulting in adverse health consequences ranging from limited to life-threatening.

Novo Nordisk has not received any reports of serious adverse events or injuries related to this recall. These products are used to lower blood glucose levels in people with diabetes and are packaged in cartons with either a vial, pen-injector (FlexPen® or FlexTouch®) or a cartridge (PenFill®). A list of the affected lots can be found in the link below.

The product can be identified by looking for the batch number or lot number located on the product or carton and matching it to the list above. Novo Nordisk has notified all physician offices that received affected samples and requested all impacted samples be returned. Customers who received an affected sample through the physician’s office should have received a letter from their physician.

If product samples match a batch number or there are any questions about the recall, please contact the Novo Nordisk recall processor Inmar at 1-888-686-5002, Monday through Friday, 9:00 AM to 5:00 PM EDT. Please report any complaints and adverse events to Novo Nordisk's Customer Care Center which can be reached at 1-800-727-6500, Monday through Friday, 8:30 AM to 6:00 PM EDT.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Check the full recall details on fda.gov

Source: FDA
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LONG TERM continued extreme immune response to Pfizer vaccine, Danville, PA, USA

Symptoms: Fever Other Chills Chest Pain Swelling
Danville, PA, USA

May 12, 2021 5:59 PM

“I am going to post my entire diary. Those who truly want to know won't mind reading the entire thing and...it's still not over yet.

Pfizer 51 day systemic reaction
(now beyond day 77)
Danville, PA


*Not a complaint*
(wasn't at the time)

I had left prior short term reviews on both do... See Moreses, now I am finally able to detail my entire reaction which was shocking to me honestly. Arthritis/fibro/immune compromised patients be advised.

After dose 1 on 3 Mar, it simply made my left hand ballooned then arthritic (never had arthritic hands before this) and it seemed as if it was going to relent, but kept coming and going, then eventually this spread to both hands and ankles. I gained 3 pounds of water weight. The pain was maddening from day 8 on, coming and going.

Day 12 I had routine nonsteroidal spinal injections. MISTAKE. I wouldn't advise doing this but it was urgent as I needed the injections to have the capability to drive to dose 2. My whole left side's injection sites swelled and scabbed over several days. (never had that happen in 12 years of receiving them) I could not sit down, lie down, or touch the sites but it resolved quickly in my opinion. The hand pain stayed the course until...

Dose 2 I was thankful to receive and looked forward to my newfound freedom. 1 Apr I had the minor eye floaters on the way home just like dose 1. I felt like a dead dog so fell asleep on the couch as soon as I walked through the door. 7 hours later developed chills and mild fever and leg (quads) pain. No big deal I thought as this happens to everyone. I began consuming electrolytes and rode the fever out with the aid of Ibuprofen. My last review ended with me saying I expect a 1 to 2 day recovery. That is not what really happened.

Following dose 2 ( lot # EP7534) I suffered an entire body inflammatory response.
The leg pain became so severe I had difficulty walking or doing anything at all for 8 days. Any attempt at physical activity doubled the pain. This is when I had my first Dr appointment and I was told to be patient and it should resolve in 2 to 4 WEEKS, and if not I need to be tested for Rheumatoid. I waited patiently and prayed for this to end. As a former athlete, I will admit to being way less sore after running a marathon.

The legs began to ease up but it traveled back to my hands, then to my lower back, then to my knees and feet. Called our Covid hotline at least 4 times during the 3 week course of this barrage and was told that this kind of reaction is almost unheard of. It then hit my hips. This was so excruciating for a week I had to lift my legs by hand to get up, and once again I could walk but didn't desire to. Next doctor appointment, was advised if the pain will not resolve in a timely manner, I need a full examination and bloodwork for gout and 7 other tests were ordered.

While laid up, incidentally my Father received dose 1 of Moderna. He was symptom free until Day 8, then, had the exact same reaction but on a lesser scale. It was then I started to believe something in our genetics is causing it. Day 52, it FINALLY began subsiding. The swelling reduced and became localized to the right knee (prior injury) and the left hand.

Overall, this was a severe reaction but I do not solely blame the vaccine. I am a 43 year old woman with Fibromyalgia and a slew of other compromising health issues. These companies did their ultimate best to save lives, perhaps mine included. Although devastated to seemingly have permanent damage to the knuckles of my left hand, tissue of the right knee and knuckles of my foot, there has been far greater devastation from Covid, including losing a family member.

I am extremely hesitant towards the booster, but I need the protection to feel at peace with sending my children back to school. I will follow my doctor's advice and the Covid team's direction to fill out the VAERS surveys for both doses. This information is found in small print on the back of the card.

*CONTINUED*

It did NOT end here either. 48 hours after the joint pain "subsided," I went to bed thinking it was all over then woke up in Tachycardia shortly after midnight with a heart rate of 156! ? For 3 days I had my daughter sleep in my bed with me as I battled a severely irregular heart beat. This was preposterous as I spent decades as a personal trainer and thought (knew!) I had a very healthy heart?

On the 3rd day of being stuck in chronic tachycardia episodes, my daughters ended up urgently calling family and an ambulance because I felt symptoms of a possible stroke.

In the ambulance my BP had escalated to 167/110 and normal for me is actually always quite low. In fact I had a reading of 117/74 the week prior during an unrelated visit. I have never had a high blood pressure reading in my entire life not from any illness or activity ever!

At the hospital I was informed my kidneys had astonishingly dropped to less than 40% of function and I was in real trouble. They stabilized me and sent me home, then a day later I went right back into tachycardia for an additional 3 days. I did the equivalent of a marathon or more each night IN MY SLEEP. I was given a heart monitor to record the activity and set up with an urgent echocardiogram and CT of my heart. With a blood clotting disorder, I could not afford to mess around any longer and had to leave my kids once again to be driven to the ER. 7 additional hours I spent with a pulse often above 150. I was finally given a Beta blocker and also an antibiotic, as the dehydration this was causing me erupted into a kidney infection which was throbbing on my right side.

I feared for me life. I feared for my vitality as my Pain treatments were stripped away due to the suspected heart condition. All my heart tests came back completely normal and I was told my heart is oddly not the source of my heart condition. A relief yes, but just further proof of how extremely and completely this vaccine attacked my body.

I was having chest pains the week prior and the week of these attacks which was finally concluded to be new Costochondritis, a rare flareup which can happen with Fibromyalgia. Thank God that's all it is but I am so through with this vaccine now and the utter devastation it has caused my entire body. I am having trouble breathing and the umpteen hospital visits have ruled out everything else. It is not anxiety but I will admit alas I have begun to grow impatient with this!! I have 1/2 dozen medical professionals in contact with me daily now working on a way to get me to the finish line.

After clearing my heart tests, I was reinstated for Pain Management and was brought in immediately for an appointment. My back underwent approximately 30 trigger point injections and there was not a location on my body without a muscle spasm. My last injections were rejected by my body due to the presence of the vaccine and I prayed this time they wouldn't be. During the procedure I suffered an immediate inflammatory response, elevated blood pressure, etc etc. My skin reacted so badly my administrator could not even apply the bandages. 13 years getting these injections and no problems until right now!

Next day it started happening all over again. My body (more specifically, the vaccine within my body) began to reject some of my treatment in the lower region. I am now being put on a steroid to combat the vaccine and widespread pain reaction of the chest, legs, hips, extremities, and back. I continue to take the Beta blocker now as well.

10 weeks of suffering I just want it to end but more importantly I have to stay vigilant in getting my story told. I'm willing to bet a reaction like this will turn out not to be so rare. In fact my Father is still laid up just the same as me he's in week 5 battling Moderna and also on a long road. My final report to the CDC will be submitted after further bloodwork, but it is to be made absolutely clear that if I have now developed an auto-immune condition...the vaccine triggered it.

Good luck to everyone but honestly weigh the decision heavily before you enter the unknown.
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Doctor Visit: Yes
Diagnosis: ER

May 13, 2021 3:03 PM

“Company name: Scentsational Soaps & Candles, Inc.
Brand name: Goose Creek, COCO TKO
Product recalled: Hand Sanitizer
Reason of the recall: Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde
FDA Recall date: May 13, 2021
Recall details: Scentsational Soaps & Candles, Inc., has volunta... See Morerily expanded its April 27 recall of scented Hand Sanitizers to include three lots of Goose Creek HAND SANITIZER (NDC 75078-004) + Aloe and one lot of COCO TKO HAND SANITIZER in 3.38 and 3.4 fluid ounce spray bottles, respectively, to the consumer level.

These products are listed in the table below. These products are being recalled after testing conducted by our firm revealed the presence of methanol (wood alcohol), benzene, and acetaldehyde. These products were sold on the Internet and distributed nationwide in the USA by Goose Creek Candles, LLC and Coconut Stand.

- Goose Creek HAND SANITZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Blueberry Limeade Anti-Bacterial Spray. UPC or NDC: NO UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe (3.38 fl oz. (100 ml)). Scent: Limoncello Anti-Bacterial Spray. UPC or NDC: NO UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Beach Dreams Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Grape Soda Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Champagne Bubbles Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Dragonfruit Splash Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Marshmallows Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Melon Picnic Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 35 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Optimistic Vibes Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Red White and Blue Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 42 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Watermelon Lemonade Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 35 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Tropical Daydream Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20260. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- COCO TKO HAND SANITIZER (3.4 fl oz. (100.55 ml)). Scent: Coconut Stand. UPC or NDC: No UPC. Lot: 20260. Retailer and States shipped: 14 cases shipped on 9/16/20 to FL.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning. Exposure to benzene can occur through inhalation, oral, and skin.

There is a reasonable probability that benzene present at levels above the maximum daily exposure recommendations can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Additionally, animal studies have shown that acetaldehyde can possibly cause cancer in humans. To date, the company has not received any reports of adverse reactions related to this recall.

These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The affected bottles of hand sanitizer include a five-digit lot code printed on the bottle near the base. The products can be identified by the label, scent, and lot code provided in the table at the end of this release. Photos are also provided at www.scentsational-products.com.

Scentsational Soaps & Candles, Inc. has notified its direct customers by telephone with confirmatory email and asked that they remove the recalled products from commerce immediately if they still had any in inventory. Consumers, distributors, and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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Brand name: Tenacore LLC
Product recalled: 2001 Tenacore Replacement CareFusion Alaris 8100 bezels
Reason of the recall: Potentially weakened elastic
FDA Recall date: April 19, 2021
Recall details: Company Announcement On February 24th, 2021, Tenacore LLC initiated a... See Morenationwide recall of 2001 Tenacore replacement CareFusion Alaris 8100 bezels due to potentially weakened plastic. A bezel with weakened plastic may, over time, lead to separation of the bezel post (recall issue) as well as other damage to the bezel (e.g., external cracking). The separation of one or more bezel posts may result in free flow, over infusion, under infusion or interruption of infusion. There is a related recall initiated by Becton Dickinson (BD). Information regarding that recall can be found using the following link: Becton Dickinson (BD) (CareFusion 303, Inc.) Recalls Alaris Pump Module Model 8100 Bezel Assembly Which Could Result in Free Flow, Over-Infusion, Under-Infusion, or Interruption of Infusion | FDA Consumers who have: Tenacore bezel parts (part number TIPA-8100-4410) with timestamp 5 and/or timestamp 6 should stop the distribution and use of these and return them to Tenacore LLC.
Alaris 8100 units that were serviced by Tenacore, or purchased from Tenacore between July 2020 and Feb 2020, should be inspected per the instructions described below to ensure that your device is not impacted. If it is, please return your device to Tenacore LLC.
Recalled bezels were manufactured from May 2020 to June 2020 and distributed from July 2020 through Feb 2021. The following products have been recalled:
Check the full recall details on fda.gov
Source: FDA
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Purchase details
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2021 Newst chainsaws-A perfect
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Reported By SafelyHQ.com User

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Reported By SafelyHQ.com User