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Influenza A (H5N1) Monovalent Vaccine, Adjuvanted Tradename: AUDENZ     (www.fda.gov)
submitted by dosvydanya_freedomz to Health 2 months ago (+1/-0)
2 comments last comment...
https://www.fda.gov/vaccines-blood-biologics/audenz

AUDENZ is an inactivated vaccine indicated for active immunization for the prevention of disease caused by the influenza A virus H5N1 subtype contained in the vaccine.
AUDENZ is approved for use in persons 6 months of age and older at increased risk of exposure to the influenza A virus H5N1 subtype contained in the vaccine.

while you watching don elon's and trump show. this has already been approved for human use
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FDA Approves Live-Virus Faggot Pox Vaccine that "can be spread to individuals who have close contact with the vaccinated individual"      (www.fda.gov)
submitted by TheodoreKent to WhatCouldGoWrong 7 months ago (+6/-0)
3 comments last comment...
https://www.fda.gov/media/75800/download?attachment

Serious complications of ACAM2000 include:
• Myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining
outside the heart). Most cases have occurred within 1-2 weeks after vaccination. Symptoms of
myocarditis and pericarditis include:
o Chest pain
o Shortness of breath or difficulty breathing
o Feelings of having a fast-beating, fluttering, or pounding heart
Symptoms of myocarditis and pericarditis may be different in children and may also include:
o Fainting
o Unusual and persistent irritability
o Unusual and persistent poor feeding
o Unusual and persistent fatigue or lack of energy
o Persistent vomiting
o Persistent pain in the abdomen
o Unusual and persistent cool, pale skin
• Inflammation of the brain or spinal cord
• Serious skin infections such as a rash caused by widespread infection of the skin (known as
eczema vaccinatum), buildup of inflamed tissue around the vaccination site that may at first
look like a bullseye and will grow into a large, non-healing sore (known as progressive
vaccinia).
• Spreading of the vaccine virus through the blood to other parts of your body
• Fetal death
• Accidental infection of the eye (which may cause swelling of the cornea causing watery painful
eyes and blurred vision, scarring of the cornea, and blindness)
• Severe allergic reaction after vaccination
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The risks for serious vaccine side effects are greater for people who:
• have heart problems or a history of heart problems
• are taking steroid eye drops or ointment
• have a weakened immune system
• have skin problems such as eczema, atopic dermatitis, burns, impetigo, contact dermatitis,
chickenpox, shingles, psoriasis, or uncontrolled acne
• are less than 1 year old
• are pregnant or become pregnant within 6 weeks after vaccination
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Health’s COVID-19 tests give false results     (www.fda.gov)
submitted by Conspirologist to Health 11 months ago (+2/-2)
0 comments...
16
FDA warns consumers not to purchase or use certain eye drops from several major brands due to risk of eye infection      (www.fda.gov)
submitted by Love240 to Health 1.5 years ago (+16/-0)
9 comments last comment...
https://www.fda.gov/drugs/drug-safety-and-availability/fda-warns-consumers-not-purchase-or-use-certain-eye-drops-several-major-brands-due-risk-eye#eyedrops

Archive link: https://archive.ph/wip/7dT4h

#Eye-Drops mentioned:
CVS Health
Leader (Cardinal Health)
Rugby (Cardinal Health)
Rite Aid
Target Up & Up
Velocity Pharma
Walmart Equate
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FDA Approves First Orally Administered Fecal Microbiota Product for the Prevention of Recurrence of Clostridioides difficile Infection     (www.fda.gov)
submitted by dosvydanya_freedomz to Health 2.0 years ago (+10/-0)
6 comments last comment...
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CONvid tests giving you bacteria now:Do Not Use Certain SD Biosensor Pilot COVID-19 At-Home Tests: FDA Safety Communication     (www.fda.gov)
submitted by dosvydanya_freedomz to Health 2.0 years ago (+3/-0)
7 comments last comment...
https://www.fda.gov/medical-devices/safety-communications/do-not-use-certain-sd-biosensor-pilot-covid-19-home-tests-fda-safety-communication

The U.S. Food and Drug Administration (FDA) is warning consumers and health care providers to stop using and throw out certain lots of recalled SD Biosensor, Inc. Pilot COVID-19 At-Home Tests, distributed by Roche Diagnostics. The FDA has significant concerns of bacterial contamination in the Pilot COVID-19 At-Home Test liquid solution, provided in the test kit. Direct contact with the contaminated liquid solution may pose safety concerns and the bacterial contamination could impact the performance of the test.
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Vaccines and Related Biological Products Advisory Committee     (www.fda.gov)
submitted by ymihere to whatever 2.7 years ago (+6/-0)
0 comments...
https://www.fda.gov/advisory-committees/blood-vaccines-and-other-biologics/vaccines-and-related-biological-products-advisory-committee

I wonder what they’ll say about coof-jabs?
October 6, 2022: FDA announced a public meeting of the Vaccines and Related Biological Products Advisory Committee (VRBPAC). This meeting will be held to discuss the strain selection for the influenza virus vaccines for the 2023 Southern Hemisphere Influenza Season.
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Fuck the mandates, time to revoke the EUA     (www.fda.gov)
submitted by Reawakened to Covid1984 3.3 years ago (+6/-0)
2 comments last comment...
https://www.fda.gov/media/144412/download

Note that it's authorized for PREVENTION.

On December 11, 2020, the Food and Drug Administration (FDA) issued an Emergency Use
Authorization (EUA) for emergency use of Pfizer-BioNTech COVID‑19 Vaccine for the prevention of COVID-19 for individuals 16 years of age and older pursuant to Section 564 of the Act. FDA reissued the letter of authorization twice: December 23, 20203 and February 25, 2021. 4

On May 10, 2021, having concluded that revising this EUA is appropriate to protect the public health or safety under section 564(g)(2) of the Act, FDA again is reissuing the letter in its entirety to authorize emergency use of Pfizer-BioNTech COVID‑19 Vaccine for the prevention of COVID-19 for individuals 12 through 15 years of age, as well as for individuals 16 years of age and older
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The FDA Safety Information and Adverse Event Reporting Program     (www.fda.gov)
submitted by ymihere to whatever 3.7 years ago (+1/-0)
0 comments...
https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program

If any one of you ever communicates with a person who thinks the medical industry can do no wrong, show them this website.