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

Covid-19 vaccine reaction, Fresno, CA, USA

2 years ago

Fresno, California, United States

Took Pfizer vaccine 3 weeks ago. had mild headache for 3 days. my two boys one had a migrane a week later other son nothing. Just had 2 shot. got mild headache and right arm felt heavy and tender and got a knot where the shot was given. also got mild nausea for a day. boys had small headache. | Symptoms: Nausea, Other, Headache

143


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


A power outage was reported in Fresno on early Tuesday morning, Mar 19. The cause of the outage was not listed. The affected area was near North Clovis Avenue. According to PG&E's outage map, Power has been restored to the area.

Outage link: pgealerts.alerts.pge.com
Source: kmph.com
Published:... See More 2024-03-19 See Less
286


According to PG&E’s outage map, about 3,186 customers are affected by a power outage in Fresno on Wednesday afternoon Mar 13. The affected area is near East Tulare Street. The outage started at 2:23 p.m. PST. The estimated time for restoration is 8:15 p.m. PST. PG&E is... See More investigating the cause of the outage. Crews are working to restore power to the area.

Outage link: pgealerts.alerts.pge.com
Source: pge.com
Published: 2024-03-13
See Less
286


A power outage impacted several businesses at the Fashion Fair in Fresno on Thursday afternoon, Mar 8. According to PG&E's outage map, the areas impacted were primarily those within the Fashion Fair site, south of Shaw Avenue and east of First Street. According to witnesses, several restaurants... See More along Shaw Avenue, including Chick-fil-A, BJ’s Restaurant & Brewhouse, the Cheesecake Factory, and Fleming’s were all without electricity. As of 4:20 p.m., power had been restored.

Outage link: pgealerts.alerts.pge.com
Source: yahoo.com
Published: 2024-03-08
See Less
286


A power outage that impacted several of the businesses at Fashion Fair in Fresno was reported by PG&E on the utility’s outage map Thursday 7th afternoon. The utility company said that it is investigating the cause of the outage, which was first reported at 11:35 a.m. Witnesses... See More say several restaurants along Shaw Avenue, including Chick-fil-A, BJ’s Restaurant & Brewhouse, the Cheesecake Factory and Fleming’s were all without electricity.

Outage link: pgealerts.alerts.pge.com
Source: yourcentralvalley.com
Published: 2024-03-07
See Less
286


Recent Interesting Reports

Received a package from Fullfillment House in Tampa. It’s a container of cream that say Subgenix. Extra strength. Not sure what it is or why I received it. No papers in the packaging See Less
523


I am a Senior living in an adult community. I just retrieved my mail and found 2 small pkgs. from SlimFit Fusion. One is Keto +ACV gummies and the other is Forskolin Extract capsules. I don't know what they are for and I did not order them.... See More

Nothing has happened so far other than receiving these two pks that I didnot order. I know this has to be a new scam but I do not know how to proceed.
See Less
20


I recieved a package in the mail through USPS Ground Advantage labeled fullfilment House P.O. Box 5708 Tampa, Fl with a small white canister labeled Verti. It appears to be some sort of metabolism supplement. I did not ever order this and don''t have any See Less
266


Received a package today from FOR RETURN ONLY containing a cheap silver cross and chain that I did not order! How do these people get my name and address? See Less
52


Scam, Yealdeals

2 weeks ago

Ordered a love seat recliner and got a pair of Gucci shades instead of a recliner See Less


I didn't order this Bee Venom from Geathers Fottys 3646 W. Wolcott Ave., Chicago, IL 60609 USA See Less


Bought a Lighter on line from a TV add that said the lighter was completely Electric and runs without any other fuel source. What I received was exactly the opposite. a Butane fueled lighter. with all the instructions in what appears to be Korean (Horizonal letters from... See More left to right) No return instructions only address is on the USPS label.
The Add on TV is way False and misleading.
See Less
1.4K


Received bottle of subgenix Bioribose. I never ordered this? From fulfillment Tampa FL. Was scammed took my ssi money almost my whole check! Help? How do I go about getting my money back? Received in mail on January 8 2024 and 154.00 was take from my account.... See More Its taken me this long to find you and company I am disabled and not good health. I can't believe this happened. I have to find way get my funds refunded. I just returned being able to looking over my account, mail ect. I see i not only one this has happened to See Less
117


Last 30 days