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Goodbye! and best wishes in your recovery

Pfizer Covid-19 Vaccine - Second Dose, Loudon, NH, USA

2 years ago

Loudon, New Hampshire, United States

Monday, 4-12-2021. It wasn't like the first one at all. I had to sit down instead of standing up compared to first shot. I could feel a bit of a pinch of shot going into my arm and it lasted a lot longer than the first one did. I've had zero pain except a little sore around the injection area. So far, so good. Later on that night had sore arm, slight headache and chills. My arm near injection area became slightly bruised due to the guy who applied pressure on injection area after my shot was finished. That was it, I didn't take Tylenol or anything because I only had minor sore arm pain for one night and chills, it went away within the next day. | Symptoms: Headache, Chills, Soreness

5


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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
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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.

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

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Company name: Pfizer
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On Thursday 29th, outages were being reported by Eversource, the state’s largest utility, as well as Unitil and the New Hampshire Electric Co-Op. Eversource reported more than 10,000 customers without power, including significant outages in Barnstead, Loudon, Hooksett, and New Boston, as well as smaller outages in... See More Rye, Nashua, Hollis, Milford, North Hampton, Concord, Weare, Brookline, Dunbarton, Amherst, and Portsmouth. The company does not report restoration times. At just after 12:30 a.m., more than 1,600 Concord and Epsom residents lost power. More minor outages, about 350, were reported in Unitil communities on the Seacoast, including Atkinson, Hampton, Hampton Falls, Kensington, and Kingston, were reported by the company.

Unitil: outage-map.unitil.com
Eversource: outagemap.eversource.com

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