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Pfizer, Austin, TX, USA

2 weeks ago

Austin, Texas, United States

After the 2nd shot my whole body has been having horrible muscle spasms. So much so that you can see them on video. They are not small, it’s not just like a little eye twitch here and there. It’s much worse when I work out and I shake after like I have some sort of neurological disorder, such as Parkinson’s. It’s been a nightmare. | Symptoms: Muscle Spasms, Shaking

1.3K


Y6
anonymous2408
I have been fighting with that since March! HBOT might help some but it is pricy. Delivers oxygen through pressure to your tissue. Check out RealNotRare.com lots like us
Reply 1 week ago

Related Reports

On Saturday November 20th, five family members got Pfizer booster vaccine. 24 Hours later one of them a 54 year old male had no symptoms. One male 26 got ver sick, vomiting, fever, muscle aches and a mouth gland very swollen, till now he has fever. A... See More 26 year old female also fever, vomiting, tight muscle chest and body aches, also swollen gland under vaccinated arm, she still feeling sick. A 33 year old also same symptoms as the female 26 year old. And me 52 years old only body and headache, and feeling better today. How long will this side effect last? I am so worried!  | Symptoms: Fever, Vomiting, Headache, Body Ache See Less
2.5K
1 Share


BM
bmg43
I understand it's quite common for individuals who are in their '20's, '30's and '40's to experience more intense symptoms to the COVID vaccines due to their younger immune systems reacting to the shots. Older people more often just experience a brief soreness at the injection site and nothing more.
Reply 4 days ago
SU
anonymous2538
This is totally normal. Vaccines produce an immune response. Immune responses can make you feel sick. Most if not all symptoms should subside in 24 - 48 hours. It tells you this in the papers they give you when you get the vaccine. Maybe try reading those instead of going straight to the internet.
Reply 4 days ago
TR
Trisha
My daughter her her BFF got this vaccine they are both 18 and 17 the first dose both sore. The 2 nd dose my daughter was fever dizzy and not feeling well I think same as her friend everyone reacts differently I think she said they got number 3 or a booster and nothing happened
Her dad got the booster and it made him sick he’s 65 … I haven’t got none yet
Reply 4 days ago
Booster shot Saturday Nov 20, 2021 Fever, body aches, all through the night. Light headless no energy diarrhea. All though Sunday Nov 21 Monday Nov 22 into Tuesday Nov 23.  | Symptoms: Diarrhea, Fever, Body Ache, Fatigue See Less
2.0K


Vaccine save lives ... it's important for everyone to get it and I hope it becomes law !
Some people get side effects others don't - same with normal flu vaccine and same with all other vaccines out there ! But they save lives - also ,... See More the moderna side effects last for 24 hours and then are gone - so please educate yourself before claiming vaccines are killing more people than Covid !
Thanks
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7.2K


A boil water notice issued last Friday and later reduced on Sunday to two streets due to a large main break has been canceled for Travis County Water District 10, officials said on Monday.

Source: cbsaustin.com
Source publication date: 2021 11 15 See Less
1.3K


A boil water notice issued last Friday and later reduced on Sunday to two streets due to a large main break has been canceled for Travis County Water District 10, officials said on Monday.

Source: cbsaustin.com
Source publication date: 2021 11 15 See Less
1.3K


All residents and businesses within an area of western Travis County are being asked to boil their water before consuming it. A water leak was found at a pump station.

This boil water notice affects people in the City of West Lake Hills and the major subdivisions... See More of Westwood, Rolling Hills West, Knollwood, Westlake Highlands, Sundown Parkway, Camelot, and the original Rob Roy Ranch.

That affects about 3,000 residential and business accounts with the water district, which equates to about 10,000 people.

Source: kvue.com
Source publication date: 2021 11 12
See Less
1.3K


All residents and businesses within an area of western Travis County are being asked to boil their water before consuming it. A water leak was found at a pump station.

This boil water notice affects people in the City of West Lake Hills and the major subdivisions... See More of Westwood, Rolling Hills West, Knollwood, Westlake Highlands, Sundown Parkway, Camelot, and the original Rob Roy Ranch.

That affects about 3,000 residential and business accounts with the water district, which equates to about 10,000 people.

Source: kvue.com
Source publication date: 2021 11 12
See Less
1.3K


Got booster, around 6 month mark after my first round. I had it the same time I got my flu shot, one in each arm. As normal some arm soreness on both arms from the shots, but zero side effects, nothing. Not sure it matters, but: I... See More am a male adult, not overweight, exercise regularly, no known health issues. | Symptoms: Soreness See Less
1.3K


DO
anonymous2372
Why would you do flu and COVID together, it’s not recommended
Reply 2 weeks ago
DW
anonymous2373
Original Poster: I googled it, and I saw a few sites saying it was no problem to get them both together, so I did it. I didn't really think much of it, or dig too deep. So if it is risky, maybe I got lucky, as so far it worked ok.
Reply 2 weeks ago
W7
anonymous2381
anonymous2372, it’s fine to get flu vaccine and COVID booster at the same time. See this recent AP article: https://apnews.com/article/coronavirus-pandemic-science-centers-for-disease-control-and-prevention-flu-immunizations-d43c118858ef108200e7b1a500e592d3
Reply 2 weeks ago
CG
anonymous2420
Don't forget to get all boosters AND the flu shots too. Life will be great in 2-5 years
Reply 1 week ago
I got the Moderna booster yesterday afternoon and had a sore arm in the evening. The day after, my arm was really hurting. I took Aleve and that relieved the pain. I also was very sleepy and slept all afternoon. I am beginning to feel better. | Symptoms: Soreness See Less
1.3K


A truck drove through an AutoZone store in Lufkin.

The truck tore through power lines during the crash. Initially, about 900 homes in the area were without power, but it is now down to just a couple dozen.

Source: ketk.com
Source publication date: 2021 11 24 See Less
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Recent Interesting Reports

Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products to the consumer level due to the presence of benzene. Internal testing identified low levels of benzene contamination in specific lots of these aerosol products.

Risk Statement: Benzene is... See More classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.

To date, Odor-Eaters® has not received any reports of adverse events related to this recall. The affected Odor-Eaters® spray products are used as antifungal and foot odor-reducing agents and are packaged in aerosol cans. See the link below for UPC, lot number and expiration dates. Refer to the image below for guidance on where to find the lot code details on the can. Forty-one lots of two Odor-Eaters® spray products (Odor-Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray) are impacted by this voluntary recall, specifically the ones listed in the link below.

The products were distributed nationwide in the United States through various retailers. Consumers, distributors, and retailers that have product which is being recalled should stop using or selling these specific Odor-Eaters® spray products and dispose of them appropriately.

Company name: Odor-Eaters®, owned by Blistex Inc.
Brand name: Odor-Eaters®
Product recalled: Oder Eaters spray products
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 17, 2021

Check the full recall details on fda.gov

Source: FDA
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101


Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared milk on the labels. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk. There have been... See More no illnesses reported to date.

During a recent FDA inspection, the firm was notified that their labels failed to disclose the presence of milk on some of their products.

The recalled products were shipped between January 2020 through November 2021 to distributors and retailers in Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Minnesota, Nevada, New Jersey, New York, North Carolina, Ohio, and Texas.

The full list of affected products is on the link below.

Lot numbers and expiration dates are found on the bottom of each container.

Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall. Nutracap will be providing corrective label stickers for product remaining in stock. Affected consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Your assistance is appreciated and necessary to prevent consumer illness.

Company Announcement Date: November 12, 2021
FDA Publish Date: November 12, 2021
Product Type: Food & Beverages. Allergens
Reason for Announcement: Undeclared Milk
Company Name: Nutracap Holdings, LLC
Brand Name: Multiple brands
Product Description: Dietary Supplements

Check the full recall details on the FDA website: fda.gov

Source: FDA
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I shipped Priority Express on Nov 15 to Essex Junction, VT and after two days it is still showing arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm. It should be delivered by Nov 16 at VT See Less
5.3K


FOR IMMEDIATE RELEASE – November 19, 2021 – American Screening LLC of Shreveport, Louisiana is voluntarily recalling 153,336 units of Hand Sanitizer, containing 70% ethyl alcohol gel to the consumer level. The hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk... See More of consumption.

Risk Statement: Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute. To date, American Screening LLC has not received any reports of adverse events related to this recall.

The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in an eight ounce bottle. The affected hand sanitizer lots include the following expiration dates of 5/21/2022 and 05/24/2022 for black capped bottles and no lot numbers or expiration dates for clear capped bottles. The product can be identified by its shape (small water bottle), with a black flip top cap or clear cap with blue pouring spout with the weight of measure of eight (8) ounces/237mL, UPC 8 4005051579 2.

The Hand Sanitizer was sold to customers & distributors Nationwide via the internet at americanscreeningcorp.com and/or in-house sales.

Consumers & distributors that have this hand sanitizer which is being recalled should stop distribution/use and return to place of purchase or discard. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to ingesting the hand sanitizer packaged in the 8 oz. water bottle style.

Company name: American Screening LLC
Brand name: American Screening
Product recalled: Hand Sanitizer
Reason of the recall: Hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption
FDA Recall date: November 19, 2021

Check the full recall details on fda.gov

Source: FDA
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CHICAGO, IL – November 19, 2021 - Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of four lots of Levetiracetam Injection, USP, to the user level. The lack of container closure integrity, found in reserve sample vials may result in a non-sterile product.

Risk Statement: Intravenous... See More administration of a product intended to be sterile that is not sterile could result in serious systemic infections which may be life threatening. 

To date, Sagent has not received reports of any product complaints or adverse events associated with this issue. Levetiracetam Injection, USP 500 mg per 5 mL, is used in the treatment of certain types of seizures and is packaged in a 5mL single-does vial. The Levetiracetam Injection, USP, label and affected lot numbers with Expiration Dates and NDC number can be found in the table below. 

Product: Levetiracetam Injection, USP / Lot Number: B0G85VB /Expiration Date: Jun-2022 / NDC Number: 25021-780-05 / Distribution Dates: May 2021 - August 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K88VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: March 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K89VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: August 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B1G194A /Expiration Date: Jun-2023 / NDC Number: 25021-780-05 / Distribution Dates: October 2021.

Product was distributed Nationwide from March to November  2021.

Company name: Sagent Pharmaceuticals, Inc.
Brand name: Sagent
Product recalled: Levetiracetam Injection
Reason of the recall: Lack of sterility assurance
FDA Recall date: November 22, 2021

Check the full recall details on fda.gov

Source: FDA
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Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared wheat, milk, soy and/or coconut on the labels. People who have an allergy or severe sensitivity to soy, milk, wheat, or coconut run the risk of serious or life-threatening allergic reaction if... See More they consume products containing soy, milk, wheat, or coconut.

On 11/4/2021 during an FDA inspection the firm was notified that their labels failed to disclose the presence of allergens on some of their products. The recalled products were shipped between June 4, 2020 through October 1, 2021 to distributors and retailers in Alabama, California, Florida, and Texas. There have been no illnesses reported to date.

The affected products are:

Brand: Boba Origin. Product: 100% Whey Protein Isolate. Flavor: Brown Sugar Milk, Tea, Undeclared milk, & soy. Size: 1 gallon plastic jar. Lot No. 2106263. Exp. 07/2023

Brand: Etedream. Product: Etegrow ISO. Flavor: Snicker Doodle, Undeclared milk. Size: 2gallon plastic jar. Lot No. 2106002. Exp. 06/2023


Brand: RAW. Product: Vegan Protein Flavor: Peanut Butter, Undeclared coconut. Size: 1gallon plastic jar. Lot No. 2108070, 2104340, 2102018, 2012304, 2010266, 2010102, 2007037/746, 2005132. Exp. 08/2023, 04/2023, 02/2023, 12/2022, 10/2022, 10/2022, 07/2022, 05/2022

Brand: Steel. Product: Veg-Pro Flavor: Cookies & Crème, Undeclared Wheat. Size: 64 ounce plastic jar. Lot No. 2109390, 2104333, 2011260, 2104007/1041, 2105059, 2011260/994. Exp. 09/2023, 04/2023, 11/2022, 04/2023, 05/2023, 11/2022

Brand: Vital Force. Product: PureISO. Flavor: Milk Chocolate, Cocoa, Undeclared milk. Size: 1gallon plastic jar. Lot. No. 2108191. Exp. 09/2023

Brand: Vital Force. Product: PureISO. Flavor: Creamy Peanut, Butter Vanilla, Undeclared milk. Size: 1gallon plastic jar. Lot No. 2109068. Exp. 09/2023

Lot numbers and expiration dates are found on the bottom of each container.

Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall.

This recall is being made with the knowledge of the Food and Drug Administration.

Company name: Nutracap Holdings, LLC
Brand name: Etedream, Vital Force, Raw, Boba Origin, Steel
Product recalled: Dietary Supplement Protein Powder
Reason of the recall: Undeclared wheat, milk, soy and/or coconut
FDA Recall date: November 09, 2021

Check the full recall details on fda.gov

Source: FDA
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5


The Procter & Gamble Company (NYSE: PG) is voluntarily recalling all lots with expiry through September 2023 of specific Old Spice and Secret aerosol spray antiperspirants and Old Spice Below Deck aerosol spray products sold in the United States, and listed in the table below, to the... See More consumer level due to the presence of benzene detected.

Risk Statement: Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Based on exposure modeling and the cancer risk assessments published by the Environmental Protection Agency (EPA) (IRIS database), daily exposure to benzene in the recalled products at the levels detected in our testing would not be expected to cause adverse health consequences. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. To date, The Procter & Gamble Company has not received any reports of adverse events related to this recall and is conducting this recall out of an abundance of caution.

The affected products are used as antiperspirants and hygiene products and are packaged in aerosol cans. See the link below for Product names and UPC codes and images for further descriptions. They are recalling all lots with expiry through September 2023 of the products listed in the link below.

Company name: The Proctor & Gamble Company
Brand name: Old Spice Secret
Product recalled: Old Spice and Secret Aerosol Sprays
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 23, 2021

Check the full recall details on fda.gov

Source: FDA
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