A former FDA official and vaccine reviewer confirms what many suspected all along. Why haven’t heads STILL rolled? #NoAccountability Hearing here:
Still no accountability at Covid-scandal-ridden federal health agencies Read More »
A physician is suing the FDA for its lack of action to inform consumers taking selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs) about potential long-term side-effects. These drugs are widely-used antidepressants. A citizen petition requests that the FDA
(READ) FDA sued for inaction on warnings about antidepressants’ sexual side effects Read More »
The following is from The Vaccine Reaction. Pfizer, Inc., the largest pharmaceutical corporation in the world marketing drugs and vaccines, has agreed to pay between $200 to $250 million to settle more than 10,000 lawsuits filed in the United States
Pfizer settles Zantac cancer lawsuits for $250 million Read More »
For whatever reason, America’s health officials haven’t seemed publicly interested in answering a crucial question: How many illnesses and deaths can be attributed to COVID versus the vaccines or some combination? Today, we look at shocking and graphic evidence that
The following is from Public Citizen. Amylyx Pharmaceuticals said on Thursday that it would withdraw AMX0035 (sodium phenylbutyrate and taurursodiol, sold as Relyvrio) from the market. A large clinical trial recently found that the drug did not provide any benefit to patients
Drug manufacturer Amylyx pulls ALS drug Relyvrio from market, citing lack of efficacy Read More »
The following is from The Vaccine Reaction. The U.S. Food and Drug Administration (FDA) is no longer requiring pharmaceutical companies to test new drugs and biologics (vaccines) on animals prior to human clinical trials and licensure. This is a change
The following information is from The Vaccine Reaction. An e-mail recently obtained by The Epoch Times reveals that the U.S. Centers for Disease Control and Prevention (CDC) drafted, but never sent, an alert to the U.S. public about the link between Covid-19
The following is an excerpt from The Defender. Clinical researchers no longer have to obtain informed consent from human subjects when their research poses “no more than minimal risk,” the U.S. Food and Drug Administration (FDA) ruled last week. The new rule
(FDA) Informed consent not required for ‘minimal risk’ studies Read More »
