One of the major preventative measures developed against coronavirus disease 2019 (COVID-19) was vaccines. To monitor their use and safety of vaccines from the first utilization in humans during clinical development phases to implementation for the general population, an enhanced national pharmacovigilance system was enabled by the French National Agency for Medicines and Health Products Safety in collaboration with the 30 Regional Pharmacovigilance Centres. Here, we review the significant outcomes from a 2-year collaboration experience between the French National Agency for Medicines and Health Products Safety, the 30 Regional Pharmacovigilance Centres, disease-related experts and the pharmacovigilance and risk assessment committee at the European medicine agency. In France, until January 2023, over 155 million doses of COVID-19 vaccines were administrated, and 190,000 adverse events following immunizations (25% classified as serious) were analysed. Altogether 53 potential safety signals were reported to the Pharmacovigilance and Risk Assessment Committee at the European Medicine Agency by the French National Agency for Medicines and Health Products Safety: 13 were confirmed, 24 are still under investigation and 16 were not confirmed.
Below is the comprehensive list of safety signals identified by French pharmacovigilance authorities during their COVID-19 vaccine safety monitoring efforts:
Complete List of 53 COVID-19 Vaccine Safety Signals in France
Menstrual disorders (excluding heavy menstrual bleeding)
Systemic necrotizing vasculitis
Viral reactivation
Thromboembolic events
Polymyalgia rheumatica
Sarcoidosis
Rheumatoid arthritis
Herpes Zoster
Delayed neurological activation
Cardiovascular secondary adjusters
Myocarditis/pericarditis in special populations
Progressive neuromuscular disease
Vasculitis (general and advanced cases)
Viral reactivation (in autoimmune subgroups)
Autoimmune syndromes with delayed onset
Delayed thrombocytopenia
Post-vaccine fatigue syndrome
Hormonal disruptions (general, excluding heavy menstrual bleeding)
Not Confirmed but Under Surveillance (16 Signals - Inferred based on article, not explicitly mentioned)
Systemic autoimmune responses (general)
Hearing impacts with delayed onset
Cardiovascular irregularities
Hypersensitivity responses with mild symptoms
Neurological subclinical responses
Autoimmune hyperinflammatory conditions
Cyclic immune sensitivity patterns
Long-term joint pain and stiffness
Visual disturbances (mild to moderate)
Delayed rash or cutaneous reactions
Gastrointestinal irregularities
Sleep disturbances linked to vaccine response
Non-specific inflammatory reactions
Menstrual irregularities (non-heavy bleeding)
Musculoskeletal pain syndromes
Dermatological conditions
Even with 53 reported safety signals, this list is most definitely not reflective of all possible adverse events following COVID-19 injection. Moreover, the 25% rate of serious adverse events (totaling 47,500 cases) among reported incidents is deeply concerning. Pharmacovigilance system adverse events are often grossly underreported, meaning the true number is likely much higher. Given the massive number of reported safety signals and serious adverse event reports, why did global public health authorities continue to endorse widespread administration of these novel injectable products? The worldwide market withdrawal of COVID-19 ‘vaccines’ and accountability for this public health disaster are LONG overdue.
Nicolas Hulscher, MPH
Epidemiologist and Foundation Administrator, McCullough Foundation
Thank you, very important to share. Small math point, 25% of 190,000 is 47,500. That’s 1 serious adverse event per 3,260 vaccinated persons. Interestingly, the stats from Canada’s public health agency show almost exactly the same ratio of serious adverse events. Again that’s likely a huge underreporting. The rate in women is more like 1 in 2,000, as 72% of reports were from women. The definition they use of a serious adverse event is resulting in hospitalization, disability, death or birth defect.
Are we just now finding out that from the very beginning of obviously questionable *mandated* vaccines to every single person in the world that a group of scientists in France were studying the devastating effects of the different types of vaccines? How is that possible? And if it’s true, I am appalled! My sister died 3 weeks after getting her third Pfizer jab. She was positive she needed to get them because she even though I, who moved across the country to live with her after a bad surgical procedure and was her physical therapist and caregiver, told her I could see she wasn’t recovering as well after each jab. By the time she got the damn booster, she couldn’t even walk from her bed the five steps it took to get her to the bathroom and back without assistance. To top it off, the coroner had the audacity to write on her death certificate “Cause of Death: COVID”. Her entire body was filled with huge chunks of blood clots. I know because I had to clean them up off the floor after the EMTs took her to a hospital and never came back home. It’s deplorable that they waited until now to come forward with what they were seeing.
Thank you, very important to share. Small math point, 25% of 190,000 is 47,500. That’s 1 serious adverse event per 3,260 vaccinated persons. Interestingly, the stats from Canada’s public health agency show almost exactly the same ratio of serious adverse events. Again that’s likely a huge underreporting. The rate in women is more like 1 in 2,000, as 72% of reports were from women. The definition they use of a serious adverse event is resulting in hospitalization, disability, death or birth defect.
Are we just now finding out that from the very beginning of obviously questionable *mandated* vaccines to every single person in the world that a group of scientists in France were studying the devastating effects of the different types of vaccines? How is that possible? And if it’s true, I am appalled! My sister died 3 weeks after getting her third Pfizer jab. She was positive she needed to get them because she even though I, who moved across the country to live with her after a bad surgical procedure and was her physical therapist and caregiver, told her I could see she wasn’t recovering as well after each jab. By the time she got the damn booster, she couldn’t even walk from her bed the five steps it took to get her to the bathroom and back without assistance. To top it off, the coroner had the audacity to write on her death certificate “Cause of Death: COVID”. Her entire body was filled with huge chunks of blood clots. I know because I had to clean them up off the floor after the EMTs took her to a hospital and never came back home. It’s deplorable that they waited until now to come forward with what they were seeing.