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Pfizer - 1st can, Fort Dodge, IA, USA
April 1, 2021 4:56 PM
Fort Dodge, 50501 Iowa, United States
Symptoms: Fatigue Soreness
- First shot
- I have not had COVID in the past
- Mild side affects included soreness in deltoid and fatigue
Symptoms: Headache Skin Rash Soreness
Denver, CO, USA
April 21, 2021 6:16 PM
“Recieved my first shot of Phizer yesterday. Hardly felt the needle insertion. I have had anaphalaxis to Tree nuts and other drug allergies, so I was scared. I did fine though. I took my anxiety medication before for panic, and did not have any bad reactions. I had a minor headache a hour later, and... painful sore arm. Arm is still sore today. I took tylenol and antihistamine after 4 hours of getting my shot. I take antihistamines for environmental allergies. Slept normal, and stayed hydrated. I had an itchy rash on my neck this morning, but it was hard to discern if it was from the vaccine or from my environmental allergies- out in the country. Still feel fine, have had my normal energy and arm is minorly sore. No other symptoms. Boyfriend also got his shot of Phizer and had sore arm as a symptom. ”
Symptoms: Fever Other Chills Fatigue Lightheaded Joint Pain Muscle Pain Soreness
New Orleans, LA, USA
April 21, 2021 10:18 PM
“2nd shot Moderna. 16 hours after shot, chills, low grade fever, muscle aches, joint pain, extreme fatigue, arm soreness. That lasted for over 18 hours. Since then heart palpitations on day 4, lightheaded, still tired. ”
Symptoms: Other Headache Swelling Sweating Body Ache Soreness
Fresno, CA, USA
April 21, 2021 10:20 PM
“First shot had some minor pain in injection site and small headache a few hours after shot, no other effects. Second shot was administered 845 a.m. I developed a headache 4 to 5 hours after, around 3 in the afternoon I started noticing pain in my arm kind of feel like my arm was a balloon but there... is no swelling just warm end a little pain that turned into me noticing my entire body was aching. Didn't get much sleep that night I noticed I had night sweats. Woke up in morning no longer had a headache or body pain ”
1 employee tested positive for Covid-19, Childcare Discovery Center, 2329 1st Ave S, Fort Dodge, IA 50501, United States
Childcare Discovery Center, 2329 1st Ave S, Fort Dodge, IA 50501, United States
September 13, 2020 12:00 PM
“One employee at ChildCare Discovery Center located on 1st Ave S in Fort Dodge tested positive for COVID-19.
Source: messengernews.net ”
Employee test positive for Covid-19, Tropical Smoothie Cafe, 2813 1/2 5th Ave S, Fort Dodge, IA 50501, United States
Tropical Smoothie Cafe, 2813 1/2 5th Ave S, Fort Dodge, IA 50501, United States
July 5, 2020 12:00 PM
“An employee at Tropical Smoothie Cafe in Fort Dodge tested positive for covid-19. If you visited this location recently, please report it and any other location that you visited.
Source: yourfortdodge.com ”
Applebee's employee tests positive for COVID-19, Applebee's Grill + Bar, 2810 5th Ave S, Fort Dodge, IA 50501, USA
Applebee's Grill + Bar, 2810 5th Ave S, Fort Dodge, IA 50501, USA
June 11, 2020 12:00 PM
“An employee at Applebee’s Grill and Bar in Fort Dodge has tested positive for COVID-19. It is unknown when the employee last worked.
Source: messengernews.net ”
Convenience store employee contracted Coronavirus, Coalville Stop-n-Shop, 23930 Boies St, Fort Dodge, IA 50501, United States
Coalville Stop-n-Shop, 23930 Boies St, Fort Dodge, IA 50501, United States
June 7, 2020 12:00 PM
“Stop N Shop in Coalville closed early Monday afternoon after learning that an employee tested positive. The employee last worked on Wednesday for a “short period of time” before being sent home. If you visited the restaurant recently, please report it and any other location that you visited.
So... urce: messengernews.net ”
Restaurant worker test positive for COVID-19, Ja-Mar Drive In Restaurant, 325 S 25th St, Fort Dodge, IA 50501, USA
Ja-Mar Drive In Restaurant, 325 S 25th St, Fort Dodge, IA 50501, USA
May 8, 2020 12:00 PM
“A Ja-Mar Drive In worker has tested positive for COVID-19. The employee last worked on Friday May, 1. If you visited the restaurant during that time, please report it and any other location that you visited.
Source: messengernews.net ”
An Employee test positive for Covid-19, Hardee's, 910 Gordon Dr, Sioux City, IA 51101, United States
Hardee's, 910 Gordon Dr, Sioux City, IA 51101, United States
April 12, 2021 12:00 PM
“An employee at Hardee's located on 910 Gordon Dr in Sioux City recently tested positive for Covid-19.
Source: siouxlandnews.com ”
Recent Interesting Reports
Symptoms: Skin Rash Muscle Pain
March 29, 2021 5:06 AM
“After I have my astrazeneca vaccine I had a bad pain in my arm for 4 days but that was not the worst part, I believe the astrazeneca triggered a bad episode of eczema as my skin was fine before the vaccine but shortly after the vaccine my skin started to flair up really badly and I’ve had to go on A... ntibiotics. Eczema is caused by an overactive immune response, I believe the astrazeneca triggered a strong immune response and in doing so triggered a outbreak of raw, bleeding skin which became infected and couldn’t Be treated with over the counter creams. I’ve been in severe pain with it for three weeks. I don’t know if it’s a coincidence but I didn’t have any signs of eczema before hand and I was eczema free for over a year. ”
Scott, AR, USA
March 24, 2021 9:25 AM
“My yar old cocker spaniel just had a seizure after giving him 2 dream bone peanut butter treats! Poor lil guy ate 2 of these shitty made in China peanut butter treats! Next thing I see is him convulsing on the floor uncontrollably! Very sad to have to watch! His half sister has been having them for... 2 years , but it’s gotta be coming from this treat. Do not ever feed your dogs these. I am devasted to now have 2 dogs that have has seizures due to this. ”
March 25, 2021 9:01 AM
“Company name: Sanit Technologies LLC d/b/a Durisan
Brand name: Durisan
Product recalled: Antimicrobial Hand Sanitizer
Reason of the recall: Due to microbial contamination
FDA Recall date: March 24, 2021
Recall details: Sanit Technologies LLC d/b/a Durisan announces a voluntary recall of the lot... s listed in the table below of Durisan Antimicrobial Hand Sanitizer, Non-Alcohol products in various sizes listed. The products are being recalled due to microbial contamination. Specifically, out of specification results for bacterial count for Burkholderia cepacia complex and Ralstonia pickettii. The issue was discovered during a routine audit focused on production scale-up during the height of the pandemic.
Check the link below for the full list of Durisan Antimicrobial Solutions Hand Sanitizer Sizes and Lot Numbers. To date, no reports of adverse reactions or customer complaints have been reported related to this recall.
The product was packaged in sizes ranging from 18mL credit cards, to bottles sized in 118, 236, 300 and 550 mL and 1000mL wall mounted dispenser refills. Pictures are available in the attached related file.
Use of a hand sanitizer contaminated with Burkholderia cepacia complex and Ralstonia pickettii, can range from no reaction to serious infections in a person with a hand wound or scrapes because the bacteria could enter the bloodstream, especially in patients with compromised immune systems. Health care professionals who use this contaminated hand sanitizer and tend to an at-risk patient, such as one with cystic fibrosis, could lead to adverse events ranging from a localized infection to lung or bloodstream infections, which could require patient hospitalization.
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. The product can be identified by examples of the product labels below. The product was manufactured from Feb. 1, 2020 until June 30, 2020, and distributed to selected retailers nationwide in the United States.
Durisan has provided written notification to its distributors and retailers and is alerting customers via this voluntary recall. Consumers that have the product which is being recalled are advised to destroy it immediately.
Consumers with questions regarding this recall can contact Durisan at 941-351-9114 [Call: 941-351-9114] , 8:30 am - 4:30 pm Eastern time, Monday through Friday or by e-mail at email@example.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
Check the full recall details on fda.gov
Source: FDA ”
Tenacore LLC 2001 Tenacore Replacement CareFusion Alaris 8100 bezels - recalled due to Potentially weakened elastic, USA
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... nationwide 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 ”
Symptoms: Headache Fatigue Soreness
Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA
April 2, 2021 7:33 PM
“The vaccine process went relatively smooth. Waited the recommended 15 minutes for any allergic reactions. Had none. My side effects have been mild. Headache, run down feeling, head fogginess, sore arm from where the vaccine was injected, alittle fatigued, and have noticed my heart rate being alittle... too high for comfort. ”
Symptoms: Fever Itching
Raleigh, NC, USA
March 29, 2021 9:50 PM
“My wife and I wanted to get the CoV2 vaccine but had significant concerns about the messenger RNA versions.
Anyway, we got the J&J vaccine, and we are satisfied with it.
However, some things need to be stated. My wife had a 103.3-degree fever the night of her shot. I didn't feel great, but the... aftereffects took longer to present themselves. While I had a slight fever, my response presented itself as bruises that itched terribly.
We are two weeks out from the vaccine, and things are going back to normal. My wife and I had to build up our stamina from the day of the shot and now (two weeks and four days ago).
Overall, we still feel that the J&J jab was the best vaccine for us. Even though this vaccine's efficacy looks less than the others, it is quite comparable if you look at the places it was tested and when it was tested.
We would highly recommend this vaccine to all who would prefer a more conventional vaccine. ”
Redwood City, CA, USA
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... nd 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 ”
Caledonia, NY, USA
April 5, 2021 4:16 PM
“I ordered a Stihl battery operated hand held saw off the internet for $37.00 and got a chain with 2 cloth handles. I would like my saw or money back. ”
March 26, 2021 7:00 PM
“Company name: Namoo Enterprise LLC
Brand name: PremierZen
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 26, 2021
Recall details: Little Ferry, NJ, Namoo Enterprise LLC is voluntarily recalling al... l lots within expiry of PremierZen Black 5000 capsules to the consumer level. FDA analysis has found the product to contain undeclared sildenafil and tadalafil. Sildenafil and tadalafil, known as phosphodiesterase (PDE-5) inhibitors, are found in FDA approved products for the treatment of male erectile dysfunction.
The presence of sildenafil and tadalafil in PremierZen Black 5000 products makes them unapproved new drugs for which the safety and efficacy have not been established and therefore subject to recall. Risk Statement: Consumers with underlying medical issues who take PremierZen Black 5000 with undeclared sildenafil and tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates.
To date, Namoo Enterprise LLC has not received any reports of adverse events related to this recall. The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in card form with one capsule per card and is aware of at least one lot with an expiration date of December 2023. Each pack is black with gold, blue, white and red text. The capsule appears black and is enclosed within clear plastic on the package. The affected lots of PremierZen Black 5000 includes all lots. PremierZen Black 5000 was sold nationwide in the USA via the internet and fulfilled by ebay at www.ebay.com and also fulfilled by amazon at www.amazon.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. Namoo Enterprise LLC is notifying its customers by this press announcement and by mailing recall letters. Consumers that have PremierZen Black 5000 should stop using and destroy them. Consumers with questions regarding this recall can contact Namoo Enterprise LLC by phone at 201-267-0539, Monday to Friday, 9 A.M. to 5 P.M. EST or email at firstname.lastname@example.org from Monday to Friday.
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. 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 ”
Lafayette, CO, USA
April 12, 2021 11:56 PM
“I have had previous allergic reactions to nuts, but am happy to report I did not experience an allergic reaction as a result of having the Pfizer vaccine. I had it at about 4-5PM, and no immediate side effects. By the late evening my arm hurt and I didn’t want to lift it. By the next morning, the pa... in had decreased, and by that evening it was completely gone. I have never had Covid before :^) ”