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Pfizer

Updated: September 16, 2022 12:59 PM
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
1.7K


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
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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
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465


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
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465


Pfizer Vacccines and boosted still got Covid and have symptoms.
Covid Positive - Tightness in chest, headache, ear pressure, no fever, sneezing, exhaustion. | Symptoms: Headache, Fatigue See Less
1.2K


SH
shePhoenyx
Out of curiosity, do you wear a mask and have you been anywhere crowded? I just want to know how paranoid I should be.
1 Reply 8 months ago
OL
anonymous3058
Out of curiosity, do you wear a mask and have you been anywhere crowded? I just want to know how paranoid I should be, as a masked, high risk person who is vaccinated and boosted with Pfizer.
Reply 8 months ago
I decided on Pfizer vs Moderna for my booster shot because of lower dose and less reported side effects. After the shot at 2pm, I got a sore arm after a few hours. Next day I had a fever around 100 and felt puny for the rest... See More of the day and went to bed. Next day I had no fever but felt below par in the morning and better as the day went by. Arm less sore 48 hours after shot but not back to normal just yet. | Symptoms: Fever, Soreness See Less
124


My whole family has it and I think so because with me it started out with a sore throat, then the next day I had a slight fever and cough along with congestion. Then the runny nose came with headaches across the eyebrow area and down the... See More nose some. I thought it was a head cold or maybe a upper respiratory type of thing. This past Monday I had to get a covid test because I was having a upper endoscopy done (very awful time for me with health issues) tuesday I got a call the procedure I can't have done because my covid test came back positive. On Tuesday I was actually getting ready to head out to have my booster covid shot. So that got put off as well. My whole family is experiencing all the same symptoms some more then the others. We are all fully vaccinated. My husband has the J&J vaccine, I had the Modena, and my kids both had Pfizer. | Symptoms: Fever, Runny Nose, Cough, Sore Throat, Congestion, Headache See Less
7.1K


Received Pfizer booster shot at 1pm, only arm pain going to bed that night. Next day had pain in bones, skin, shivering, weakness 8 hrs and counting.  | Symptoms: Weakness See Less
8.8K


XI
anonymous2742
I know this will sound weird but start taking hot baths and put in 1 Cup Borax Detergent, 1 Cup of Peroxide, 1 Cup of Baking Soda and 1Cup of Epson Salt. This will help pull all of the metals out of your body that they put in those shots, they are very harmful to your body and needs to be pulled out, this is basically a detox mixture. Get the bath as hot as you can stand, then soak for a bit. Make sure to shower and wash afterwards. Repeat until you can feel your body get back to normal.
-1 Reply 9 months ago
MK
anonymous2743
Give it 24 hrs. All side effects will disappear.
1 Reply 9 months ago
CE
CeeCee
To anonymous2742, STOP spreading misinformation! None of the Covid vaccines available in the U.S. contain any metals.
Reply 9 months ago
XV
anonymous2756
How can you be certain of this Cee Cee? Have you completed analytical studies?
Reply 9 months ago
My daughter and I had our Pfizer booster shot. We both had sore arms. We both had a mild upset stomach that only lasted a day. We're both happy that we were able to get our boosters. | Symptoms: Other See Less
8.8K


About 6 minutes after taking second pfizer dose, I began to sweat, blood pressure dropped, nausea set in and almost lost consciousness a couple of times. A nurse and a doctor stayed with me and offered some water. That didn't help ad after about an hour, I... See More was taken by ambulance to emergency room and treated with fluids and anti-nausea feeds. About 5-6 hours later I began to feel better and went home. | Symptoms: Nausea, Sweating See Less
4.8K
1 Share


SI
anonymous2659
I hope you are going to be ok. How are you feeling now?
1 Reply 9 months ago
DU
anonymous2660
This sounds like allergic reaction and a terrible thing to post on this forum as it enables the narrative that the vaccine “kills/harms” because a TINY fraction of the population has a severe/bad reaction. Your immune system just sounds weak, the simple fact you were given fluids and fully recovered exemplifies that.
People aren’t even reading everything, they read the first part and “oH gOd aRe yOu OkAy” when CLEARLY you are.
-1 Reply 9 months ago
OF
anonymous2692
Its exactly the right place to post side effects . So others can be aware of possible side effects .
1 Reply 9 months ago
XJ
anonymous2666
sounds like anxiety
-1 Reply 9 months ago
5L
anonymous2676
What in the actual heck is wrong with the people who are so crazy about these jabs and putting down anyone who has a reaction? I have to believe that they are paid spokespersons or something, like who tells someone their reaction is because they are weak... seriously anonymous2660, people have legitimate reactions and concerns and this is the place to voice them, and yet people like you belittle them, what is that even about?
1 Reply 9 months ago
XY
anonymous2682
I love all the comments saying it’s anxiety. I know many people with Heart conditions that they will have the rest of their lives. These reactions are not normal.
Reply 9 months ago
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