Pfizer Covid Vaccine Experience, Cleveland, OH, USA

3 years ago •reported by user-gvfx4397

Pfizer Covid Vaccine Experience, Cleveland, OH, USA

Cleveland, Ohio, United States

I have a history of food and drug allergies, so I had some anxiety about this, but my experience was actually pretty great.

My arm soreness with the covid vaccine was less duration than it is with flu or tetanus.

Soon after the 1st covid vaccine dose, the pain in my bicep was pretty intense within a few hours, and also I had some throbbing in my armpit (axillary lymph nodes swelling a bit) and odd ache in my leg joints...it makes no sense...maybe the hip and leg joint pain wasn't related, could have been sitting oddly when nervous, or something, not sure.

I did have a dime or nickel sized red dot near the vaccine site, not sure when it appeared, I didn't see it until about 1-2 hours post-vaccination when i removed the bandaid, but the spot disappeared within hours. About the same time the spot resolved is when the armpit throbbing/swelling resolved, too.

Anyway, the arm pain and armpit swelling resolved mostly within 24 hours, completely gone by 48-60 hours, so that was great. Flu shot pain lasts almost a week for me, and tetanus shot pain lasts a week, so this seems less intense than those other vaccines. With flu and tdap, i'll wake up in the night if i roll over on that vaccinated arm, but that didn't happen with this vaccine. Covid vaccine was very painful in bicep for about 6 hours, then quickly minimized to become less painful than flu shot and tdap shot.

I did feel fatigued the next day, but overall, my symptoms were milder than after the flu vaccine, but I am expecting the 2nd dose to cause more of a reaction.

Overall, my experience was good, was as I expected it to be. I did expect to experience some symptoms, so I wasn't concerned. | Symptoms: Fatigue, Body Ache, Joint Pain, Muscle Pain, Soreness, Swelling

#featuredcovid19vaccinereports #pfizer #vaccine #pfizercovid19vaccine #covid19vaccine #cleveland #ohio #us #roll

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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
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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
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Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-issues-voluntary-nationwide-recall-one-lot-propofol-injectable-emulsion-containing-benzyl
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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
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The recalled product is:
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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.

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FDA Recall date: July 13, 2022

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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.

- Accureticâ„¢ (quinapril HCl/hydrochlorothiazide) tablets, 10/12.5 mg
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Pfizer has notified direct consignees by letter to arrange for return of any recalled product.

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