1malumprohibitum wrote: “Seriously? HCQ has been in constant use for DECADES. We know everything there is to know about it. It is absolutely safe for just about everyone. You cannot even compare an experimental gene therapy to that. It’s ridiculous”
It is hypocritical to criticize the vaccines for not being approved without also criticizing HCQ for not being approved.
FWIW:
Hydroxychloroquine is associated with several rare but serious adverse reactions that may warrant immediate discontinuation of the medicine.
Serious adverse reactions include ophthalmological, cardiomyopathy and QT prolongation, haematological, and neurological and neuromuscular reactions.
Nor, has HCQ been shown to be effective in treating COVID. At one time there was an EUA for HCQ for COVID but that was withdrawn.
15 Jun 2020. The U.S. Food and Drug Administration (FDA) revoked the emergency use authorization (EUA) that allowed for chloroquine phosphate and hydroxychloroquine sulfate donated to the Strategic National Stockpile to be used to treat certain hospitalized patients with COVID-19 when a clinical trial was unavailable, or participation in a clinical trial was not feasible. The agency determined that the legal criteria for issuing an EUA are no longer met. Based on its ongoing analysis of the EUA and emerging scientific data, the FDA determined that chloroquine and hydroxychloroquine are unlikely to be effective in treating COVID-19 for the authorized uses in the EUA. Additionally, in light of ongoing serious cardiac adverse events and other potential serious side effects, the known and potential benefits of chloroquine and hydroxychloroquine no longer outweigh the known and potential risks for the authorized use. This is the statutory standard for issuance of an EUA. The Biomedical Advanced Research and Development Authority (BARDA) within the U.S. Department of Health and Human Services originally requested the EUA covering chloroquine and hydroxychloroquine, and the FDA granted the EUA on March 28, 2020 based on the science and data available at the time. Today, in consultation with the FDA, BARDA sent a letter to the FDA requesting revocation of the EUA based on up to date science and data.
The arguments about its risk were generated once President Trump talked about the drug.