I’ve been in the Pharmaceutical industry for the past 7-8 years and I’ve come to realize how scary and disappointing it is to know that most of the “unreal data” that is collected to utilize for FDA approval on vaccines. It’s sad to know that most of the participants that volunteer in research, are actually just doing it for the compensa…
I’ve been in the Pharmaceutical industry for the past 7-8 years and I’ve come to realize how scary and disappointing it is to know that most of the “unreal data” that is collected to utilize for FDA approval on vaccines. It’s sad to know that most of the participants that volunteer in research, are actually just doing it for the compensation and don’t report true data and sometimes don’t report at all. These COVID vaccines were approved way too fast and the only data that was collected for safety reports, were questionnaires completed by the participants through a mobile application. There were no safety labs, or electrocardiograms performed for any of these participants… how is that safe for anyone. If these vaccines were approved by a organization that supposedly “protects and secures the safety of humans” then basically we can’t trust these vaccines that are put out on the market. It’s actually killing people…. It’s sad to know that it’s all false and we can’t trust the medical industry nor the pharmaceutical industry. Actions speak louder, and after seeing it with my eyes, it’s been proven that at the end of the day what matters the most to everyone and what’s more important, is money and not our health nor future. I used to love working in the pharmaceutical industry and I wanted to be a part of a good change and help create treatments and save lives. Now, I’m just disappointed and don’t want to be a part of a big lie….
If I can make a suggestion to possibly prevent this from continuing, is that the pharmaceutical companies should enforce real safety assessments in their protocols and the IRB should be much more strict before approving these protocols. •Assuring that there will be safety assessments performed on a regular basis like; safety labs, ECGs, x-rays for the lungs. This should help collect safety and reliable data.
•It would make the FDA’s job much easier on approving ”true and safe data ” in our research trials.
I’ve been in the Pharmaceutical industry for the past 7-8 years and I’ve come to realize how scary and disappointing it is to know that most of the “unreal data” that is collected to utilize for FDA approval on vaccines. It’s sad to know that most of the participants that volunteer in research, are actually just doing it for the compensation and don’t report true data and sometimes don’t report at all. These COVID vaccines were approved way too fast and the only data that was collected for safety reports, were questionnaires completed by the participants through a mobile application. There were no safety labs, or electrocardiograms performed for any of these participants… how is that safe for anyone. If these vaccines were approved by a organization that supposedly “protects and secures the safety of humans” then basically we can’t trust these vaccines that are put out on the market. It’s actually killing people…. It’s sad to know that it’s all false and we can’t trust the medical industry nor the pharmaceutical industry. Actions speak louder, and after seeing it with my eyes, it’s been proven that at the end of the day what matters the most to everyone and what’s more important, is money and not our health nor future. I used to love working in the pharmaceutical industry and I wanted to be a part of a good change and help create treatments and save lives. Now, I’m just disappointed and don’t want to be a part of a big lie….
If I can make a suggestion to possibly prevent this from continuing, is that the pharmaceutical companies should enforce real safety assessments in their protocols and the IRB should be much more strict before approving these protocols. •Assuring that there will be safety assessments performed on a regular basis like; safety labs, ECGs, x-rays for the lungs. This should help collect safety and reliable data.
•It would make the FDA’s job much easier on approving ”true and safe data ” in our research trials.