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I am reporting Moderna reaction, Oxford, OH, USA

April 9, 2021 5:54 PM

Oxford, 45056 Ohio, United States

Symptoms: Nausea Fever Headache Body Ache Muscle Pain

After the second shot. I had fever, nausea, headache, my body throbbed with muscles aching and fever above 100f. It took me almost 36 hrs to recover

Reported By SafelyHQ.com User

Related Reports

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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Reported By SafelyHQ.com User

Pfizer Vaccine 1st dose, Bowmanville, ON, Canada

Symptoms: Other Soreness
Bowmanville, ON, Canada

May 13, 2021 1:23 PM

“Received 1st dose of Pfizer vaccine on May 08 2021. Today is May 13. Symptoms the same as when I get a flu shot. Sore arm for 24 hours and felt tired the 2nd day. I have allergies to Sulpa drugs and anti-inflammatories - had to wait for 30 minutes on site after injections to see if I had a reactio... See Moren. Nothing happened. :) See Less
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Vaccination - J&J Info, Portland, OR, USA

Symptoms: Fever Fatigue Soreness
Portland, OR, USA

May 13, 2021 7:57 PM

“I am a woman in her 50's and I received the J&J vaccine on Monday 05.10.21 felt good right after arm a bit sore. The next day pretty fatigued low grade fever. See Less
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March 16, 2021 9:23 AM

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Covid-19 OSHA Complaint, NT Techno USA Corporation, 3124 Montague Centre Road, OXFORD, NC, 27565, USA

NT Techno USA Corporation, 3124 Montague Centre Road, OXFORD, NC, 27565, USA

March 10, 2021 12:00 PM

“Employees could be exposed to the COVID-19 virus in the workplace, due to: 1. At least 6 employees are sick with the virus, and the number is rising; 2. The employer is not informing employees when other employees, with whom they have had close contact, have tested positive for the virus, and/or hav... See Moree been diagnosed with the infection; 3. The workplace is not being cleaned/sanitized; 4. Employees cannot keep 6 feet apart at their work stations.


Source: Osha.gov | Receipt Date: 2021-01-25
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Covid-19 OSHA Complaint, T&D SPECIALTIES, INC., 35 INDUSTRIAL PARK RD EAST, OXFORD, MA, 01540, USA

T&D SPECIALTIES, INC., 35 INDUSTRIAL PARK RD EAST, OXFORD, MA, 01540, USA

February 23, 2021 12:00 PM

“Stock delivered to loading dock area temporarily partially block walkways and exits until stock is put away.

Alleged Hazards: 2, Employees Exposed: 5
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Covid-19 OSHA Complaint, NT Techno USA Corporation, 3124 Montague Centre Rd, OXFORD, NC, 27565, USA

NT Techno USA Corporation, 3124 Montague Centre Rd, OXFORD, NC, 27565, USA

January 13, 2021 12:00 PM

“1. Employees have been sick at work while being exposed to relatives which have tested positive for COVID-19. The employer does not want to disclose the information. 2. Employees are concerned about exposure to heavy oil mist, while working in an enclosed area without ventilation.


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Covid-19 OSHA Complaint, Granville Opco, LLC dba The Granville House, 200 Coventry Drive, OXFORD, NC, 27565, USA

Granville Opco, LLC dba The Granville House, 200 Coventry Drive, OXFORD, NC, 27565, USA

January 13, 2021 12:00 PM

“1. There has been an outbreak of COVID-19 over the last two weeks, involving residents and employees. Employees wear personal protective equipment, but cases seem to keep rising. There is concern that there is no sanitation protocol being used and proper measures are not being taken to minimize the... See Morespread of the virus. 2. During testing for the virus, which is done every week, hands are not being washed and gloves are not being changed in between each test.


Source: Osha.gov | Receipt Date: 2020-11-24
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Covid-19 OSHA Complaint, Granville County - Department of Social Services, 410 West Spring Street, OXFORD, NC, 27565, USA

Granville County - Department of Social Services, 410 West Spring Street, OXFORD, NC, 27565, USA

December 15, 2020 12:00 PM

“1. There have been two cases of COVID-19 in a week at the facility. There are no supplies to clean and sanitize and the facility is not being closed for cleaning. Employees are concerned of being exposed to the virus. 2. Employees are working in small offices with two or people in each office so tha... See Moret social distancing is not feasible.


Source: Osha.gov | Receipt Date: 2020-11-12
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Recent Interesting Reports

2nd Dose Pfizer Vaccine, Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA

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Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA

April 21, 2021 6:01 PM

“Day 1 after vaccination my symptoms were a headache, nausea, medicine head, dizzy spells and alittle fatigue. Day 2 after my second dose. My symptoms include the following, sore painful arm, nausea, slight headache, medicine head, body & muscle aches, lymph nodes appeared to be inflamed which caused... See Moremy ears to hurt. Felt like I had a mild case of the flu. Been miserable and missing 2 days of work because of this. See Less
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May 12, 2021 8:00 PM

“Company name: Dibar Nutricional S. de R.L. de C.V.
Brand name: DIBAR Labs, ProtectoRx
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 12, 2021
Recall details: Company Announcement Morelia, Michoacán, Mexico, Dibar Nutricional S. de R.L. De C.V. (... See More“Dibar”) is voluntarily recalling 27 lots of DIBAR Labs Hand Sanitizer packaged in 8oz (8-53090-00301-3 UPC) and 16 oz (8-53090-00302-0 UPC) fluid ounce bottles, respectively, to the consumer level. (See products listed in the link below in Table 1 and Label 1). Dibar is also voluntarily recalling 2 lots of ProtectoRx Hand Sanitizer packaged in 2oz (Lot Number LDHSN050720) and 16oz (Lot Number LDHSN050820) fluid ounce bottles, respectively, to the consumer level. (See products listed in the link below in Table 2 and Label 2). These products are being recalled after testing conducted by our firm revealed the presence of methanol. 

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.

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 twelvedigit 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. These products were distributed nationwide in the USA through S.E.N.D. LLC and its customers (Click in the link below Table 1). Products labeled as ProtectoRx Hand Sanitizer were distributed in Puerto Rico through PR TRADING LLC and its customers (Click in the link below Table 2.). Dibar Nutricional S. de R.L. De C.V., has notified its direct distributors by a letter 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.

Consumers with questions regarding this recall can contact our Commercial Offices, +52 443-314-5369, M-F, during business hours 9:00 a.m. – 6:00 p.m. ET and/or email us to QA@dibarlabs.com.  Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product. 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.

- Complete and submit the report Online.
- Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. (Table 1. Lots distributed to S.E.N.D. LLC and its customers)  

Check the full recall details on fda.gov

Source: FDA
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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

May 11, 2021 3:01 PM

“Company name: Dash Xclusive
Brand name: Imperia Elita
Product recalled: Vitaccino Coffee weight loss and anxiety dietary supplement
Reason of the recall: Undeclared Sibutramine and Fluoxetine
FDA Recall date: May 11, 2021
Recall details: Glendale, California, Dash Xclusive is voluntarily recal... See Moreling all lots of Imperia Elita Vitaccino Coffee to the consumer level. FDA analysis has found the product to contain undeclared sibutramine and fluoxetine. Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues, including stroke, heart failure and serious health risk especially to those with underlying heart related disease.

Fluoxetine is an FDA approved drug indicated for the treatment of various depressive disorders, obsessive compulsive disorder, bulimia and panic disorders. This drug product carries a box warning for suicidal thoughts and behaviors and it needs to be monitored closely by a prescriber. The presence of sibutramine and fluoxetine in Imperia Elita Vitaccino coffee renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. Dash Xclusive has not received any reports of adverse events related to this recall.

Risk Statement: Products containing undeclared sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. Products containing undeclared fluoxetine could cause suicidal thinking and behavior, an accumulation of high levels of serotonin in the body or neuroleptic malignant syndrome (NMS)-like reactions which is a life-threatening neurological disorder; elevated mood state that can cause higher than normal energy levels, restlessness, decreased need for sleep; abnormal bleeding, and low sodium levels.

The product is marketed  as a dietary supplement for weight loss and is packaged in a black rectangular box and contains fifteen sachets. The affected Imperia Elita Vitaccino coffee lots include all lots. Product was distributed Nationwide in the USA via internet and by ebay at www.ebay.com. On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.

Dash Xclusive is notifying its customers by e-messages on the eBay platform and is arranging for return of all recalled products. Consumers that have Imperia Elita Vitaccino Coffee which is being recalled should stop using/return to Dash Xclusive, 610 S. Verdugo Road, Apt 31, Glendale, California 91205. Consumers with questions regarding this recall can contact Dash Xclusive by e-mail at dashxclusive11@gmail.com on Mondays to Thursdays from 11am to 4pm Pacific Time zone. 

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. 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. Complete and submit the report Online. Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. 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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April 18, 2021 10:04 AM

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Doctor Visit: Yes
Diagnosis: Hospital

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

SCAM, Alameda, CA, USA

Alameda, CA, USA

May 4, 2021 2:10 PM

“I bought a battery powered woodcutting saw from Kenyak. I recieved a chain with two rings. How can we stop these people. I bought this a couple months ago and today the ad is still running on USA today. Please help. Please stop these people. The add is still on USA today See Less
Reported By SafelyHQ.com User

April 28, 2021 7:00 PM

“Company name: Scentsational Soaps & Candles, Inc.
Brand name: Ulta Beauty Collection & SS
Product recalled: Scented Hand Sanitizer
Reason of the recall: Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde
FDA Recall date: April 28, 2021
Recall details: Scentsational Soaps & Candles, I... See Morenc., is voluntarily recalling 5 lots of Scentsational Soaps & Candles scented Hand Sanitizers from the Black and White Collection and Photo Real Collection and 3 lots of Ulta Beauty Collection scented Hand Sanitizer Spray packaged in 3.38 and 3.4 fluid ounce spray bottles, respectively, to the consumer level. See products 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 distributed nationwide in the USA through Ulta Beauty, TJ Maxx, and Marshalls retail stores.

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 or, in the case of the Ulta Beauty Collection product, a five-digit lot code followed by a single letter. 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 attached to this notice.

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.

Ulta Beauty has confirmed it has removed the recalled Ulta Beauty Collection product from its stores and online. Consumers with questions regarding this recall can contact our Customer Support Desk, 1-855-554-8050, M-F, during business hours 9:00 a.m. – 5:00 p.m. ET.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product. 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.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. “As the owners of the company, my wife and I want to reassure consumers and our customers that we are doing absolutely everything possible to carry out this recall efficiently and effectively and ensure it does not happen again.” said Steve Morrison of Scentsational Soaps & Candles, Inc.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

April 29, 2021 5:31 PM

“I ordered a "Battery-Powered Wood Cutter x 1". The picture of my order was very similar to the one next to this report I am making. They sent me an email back telling my they had two options on the page and I chose to pay for some chain looking thing that looks like you can kill someone with it. And... See Morethey refuse to give me my money back. I have the order, email correspondence and photos of the product I ordered. They advertise in very large photos one thing and then have a very small photo in the corner of something else. You had no idea was even there. Until you don't get what you ordered, but in stead you get the tiny thing in the corner. I can supply all this to you if you can stop these thieves from continuing there false business practices. See Less
Reported By SafelyHQ.com User

April 19, 2021 9:01 PM

“Company name: Tenacore LLC
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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Reported By SafelyHQ.com User