Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case! Your contact information is not shown on the website.
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please accept our Terms & Conditions

We do not show your email or contact info

Please provide email or phone
Please provide email or phone
Add photos or video
We recommend photos and videos to help explain your report
Add Photo/Video
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!
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)
Goodbye! and best wishes in your recovery
Visit our learn pages for more helpful information or, email us: support@safelyhq.com
Report by
Loading...
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

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)

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Pfizer vaccine, Hermosa, Chicago, IL, USA

3 years ago

Chicago, Illinois, United States

Pfizer vaccine. was extremely fatigued for about 4 days. | Symptoms: Fatigue

1.6K


Related Reports

I got this covid booster, and flu shot at the same time. Zero side effects so far, and I am on day 3 now. I assume by now I am in the clear. The picture says moderna, but he assured me it was the pfizer. See Less
544


Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion (containing benzyl alcohol), 100mL Single Patient Use Glass Fliptop Vial; lot EA7470, to the user level due to visible particulates observed in two vials during annual examination of retention samples. The product lot... See More was distributed nationwide to wholesalers/hospitals in the United States from July 16, 2020 through July 24, 2020. To date, Pfizer has not received reports of any adverse events associated with this issue for this lot.

Risk Statement: Patients receiving the impacted product have a remote probability of experiencing potential adverse events, such as blockage of blood vessels, including decreased blood flow to the brain, heart attack, pulmonary embolus, and tissue necrosis. Hypersensitivity reactions and transmission of infectious disease can also occur.

Propofol is an intravenous general anesthetic and sedation drug for use in the induction and maintenance of anesthesia or sedation. Propofol Injectable Emulsion is a terminally sterilized (TS) product. It is a sterile, nonpyrogenic emulsion containing 10 mg/mL of propofol suitable for intravenous administration supplied in a Single Patient Use Glass Fliptop Vial. The NDC, Lot Number, Expiration Date, and Configuration details for Propofol Injectable Emulsion are indicated below.

Product: Configuration/Count Propofol Injectable Emulsion, 100 mL Single Patient Use Glass Fliptop Vial
NDC: Vial: 0409-4699-54 Tray: 0409-4699-24
Lot Number: EA7470
Expiration Date: 01 JUNE 2023
Presentation: 1g/100 mL, Single Patient Use Glass Fliptop Vial
Configuration/Count: Tray of 10 Units

Pfizer places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Pfizer has notified direct consignees by letter to arrange for return of any recalled product.

Wholesalers or hospitals with an existing inventory of the lot, which is being recalled, should discontinue use, stop distribution and quarantine immediately. If you have further distributed the recalled product, please notify your accounts and/or any additional locations which may have received the recalled product. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.

Company name: Hospira, Inc., a Pfizer Company
Brand name: Hospira
Product recalled: Propofol Injection Emulsion, USP
Reason of the recall: Potential presence of visible particulate
FDA Recall date: August 22, 2022

Source: fda.gov
See Less
303


Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol), 100 mL Single Patient Use Glass Fliptop Vial; lot DX9067, to the user level due to a visible particulate observed in a single vial during annual examination of retain... See More samples. The product lot was distributed nationwide to wholesalers/ hospitals/Department of Defense in the United States from June 10, 2020 through June 26, 2020.

The recalled product is:
- Propofol Injectable Emulsion, USP 100 mL Single Patient Use Glass Fliptop Vial, NDC: Vial: 0409-4699-54 Carton: 0409-4699-24, Lot Number: DX9067, Expiration Date Presentation: 01 MAY 2023, Configuration/Count: 1 g/100 mL, Single Patient Use Glass Fliptop Vial Case of 10 Units.

Risk Statement: Patients receiving the impacted product are at risk of experiencing life-threatening adverse clinical effects including but not limited to: blockage of blood vessels, including decreased blood flow to the brain, heart attack, pulmonary embolus, and tissue necrosis. Hypersensitivity reactions and transmission of infectious disease can also occur.

To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for this lot. Propofol is an intravenous general anesthetic and sedation drug for use in the induction and maintenance of anesthesia or sedation. Propofol Injectable Emulsion, USP is a terminally sterilized (TS) product. It is a sterile, nonpyrogenic emulsion containing 10 mg/mL of propofol suitable for intravenous administration supplied in a single patient use fliptop vial.

Wholesalers or hospitals with an existing inventory of the lot, which is being recalled, should stop use and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or hospital level/institution, 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.

Company name: Hospira Inc, A Pfizer Company
Brand name: Hospira
Product recalled: Propofol Injection Emulsion, USP
Reason of the recall: Potential presence of visible particulate
FDA Recall date: July 13, 2022

Source: fda.gov
See Less
303


Pfizer is voluntarily recalling Accuretic (quinapril HCl/hydrochlorothiazide) tablets distributed by Pfizer as well as two authorized generics distributed by Greenstone (quinapril and hydrochlorothiazide and quinapril HCl/ hydrochlorothiazide) to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-quinapril, above the Acceptable Daily Intake (ADI) level.... See More To date, Pfizer is not aware of reports of adverse events that have been assessed to be related to this recall. 

Pfizer will recall six lots of Accuretic tablets, one lot of quinapril and hydrochlorothiazide tablets and four lots of quinapril HCl/ hydrochlorothiazide tablets. Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables. Everyone is exposed to some level of nitrosamines. These impurities may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time.

These products are indicated for the treatment of hypertension.  Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. The products have a safety profile that has been established over 20 years of marketing authorization and through a robust clinical program. Pfizer believes the benefit/risk profile of the products remains positive based on currently available data. Although long term ingestion of N-nitroso-quinapril may be associated with a potential increased cancer risk in humans, there is no immediate risk to patients taking this medication. Patients currently taking the products should consult with their doctor about alternative treatment options.

The NDC, Lot Number, Expiration Date, and Configuration details for these products are indicated in the tables in the link below and photos of the products can be found below. The product lots were distributed nationwide to wholesalers and distributors in the United States and Puerto Rico from November 2019 to March 2022.

- Accuretic™ (quinapril HCl/hydrochlorothiazide) tablets, 10/12.5 mg
- Accuretic™ (quinapril HCl/hydrochlorothiazide) tablets, 20/12.5 mg
- Accuretic™ (quinapril HCl/hydrochlorothiazide) tablets, 20/25 mg
- quinapril and hydrochlorothiazide tablets, 20/25 mg
- quinapril HCl/hydrochlorothiazide tablets, 20/12.5 mg
- quinapril HCl/hydrochlorothiazide tablets, 20/25 mg

Pfizer has notified direct consignees by letter to arrange for return of any recalled product.

Wholesalers and distributors with an existing inventory of the lots, listed in the table above, should stop use and distribution and quarantine the product immediately.

If you have further distributed the recalled product, please notify any accounts or additional locations which may have received the recalled product from you.

Company name: Pfizer
Brand name: Accuretic, Greenstone Brand
Product recalled: Accuretic™ (quinapril HCl/hydrochlorothiazide); quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets
Reason of the recall: Presence of a nitrosamine, N-nitroso-quinapril
FDA Recall date: March 22, 2022

Source: fda.gov
See Less
303


Mailman had this package w my normal mail delivery. I opened the package to see this supplement inside which I have not ordered. Came from Fullfillment House Tampa, Fl See Less
1.6K


I have received two packages that I did not order. I do not want them and I am not sure I should return them. I do not want to pay any shipping fees. Both packages were addresses to me and shipped by Geathers Fotty, 3646 S Wolcott... See More Ave, Chicago, IL. I am very concerned about these deliveries and why I am receiving them. I have checked my records and I have not been charged anything at this time. Should I report this to the shipper USPS? Please keep me posted. See Less
368


According to the Commonwealth Edison Company outage map, a power outage affected 168 customers in West Town, Chicago on Tuesday morning, Mar 19. The estimated time for restoration is 11:30 a.m. The cause of the outage is equipment maintenance. Crews are working to restore power to the... See More area.

Outage link: comed.com
Source: comed.com
Published: 2024-03-19
See Less
1.6K


On Sunday March 15th 2024 I received a package 📦 with 2 sandal wood essential oil with no packaging slip in closed, that I did not order from Heathers Fottys I don't see a charge on my bank statement I don't know why they sent this to... See More me and I hope they're not going to charge me for it on my card later in time because I don't know how they would have gotten my information. I don't know if this is a scam, but evidently other people are receiving products from this same company and did not order them as well, according to their statements. I can't find a phone number to contact them this is really weird because they could send you items and then charge you whatever they want later for them, so I hope this is not the case. See Less
368


Recent Interesting Reports

I ordered the 3 bras and they are too small, plus a plastic support was coming out. I was really sad about the fit.
I ordered 3 bras and I just received them and the are too small. After reading your reports, I guess that I won't... See More get a refund from Heathers Motty. Guess I just learned a costly lesson. See Less


service@sinuette.com, Ordered from a site that said KOHL'S Discount Store. It was sinuette and they were from overseas. They told me that they shipped the order twice and I received NOTHING! They said it was too expensive to ship again, but they could only give me a... See More 30% refund, which I have never seen!! FRAUD SCAM See Less
115


I haven't opened it. I plan to return it. This is the information I received when I searched for Heather's Motty. I saw a special type of bra advertised through YouTube. Within a twelve hour period or even much less, I looked up the company on Google.... See More I wanted to contact the company to cancel my order. The information given on the order receipt provided a unanswerable phone number to contact. When I replied to the email address given, the response was there is no such email. The report of people's response is very poor. I then contacted my bank. A dispute is under investigation. I just received the package yesterday. My bank contacted me asking me if I received it. I just did yesterday. I plan to return it today. But the company I thought I was ordering from is totally different. The bras stated they were specifically designed to help people with lymphedema issues, which I have as a result of surgery. See Less
2.9K


I am reporting these keto+acv gummies… these are not the ones in the picture. I was supposed to be charged $39.76 u buy 3 bottles and get 2 free. But, yet I was charged $198.78. The gummies are not what was in the picture and the charged... See More was incorrect.

They also had a video picture of the Shark Tank lady the one with the long blonde hair. Also a video with Kelly Clarkson. Then they charged my card after I canceled the order.

PO Box 81827 Las Vegas NV 89180-1827
See Less
1.4K


I did not order this Verti powder and it came in a bubble wrap package with no receipt. Return address was Tampa Fl See Less
1


I am also scammed. Ordered 3, I cancelled the order as they do not have anything in stock, they promised me a refund into my paypal account of $486, which the never did, then they send the products, it is so tiny with a very weak computer... See More fan inside, cannot even feel a breeze on my face. They are scammers, I have reported them to Paypal, but still waiting. See Less


I ordered 5 products from a facebook page, namely 3 blouses and 2 pairs of pants and received only 3 blouses, which do not correspond either in appearance or size, with a musty smell. When I searched for the email address on awb to return the products, I did not find it. See Less
3


Last 30 days