Black People : Remdesivir Side Effects - What all was reported. Not FDA approved has been used in treatment of Covid ( China discontinued due to adverse effects )

HODEE

Alonewolf
PREMIUM MEMBER
Jul 2, 2003
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Hydroxychloroquine - was taken by the President he stated many times.. So according to this article Remdesivir is less likely to be effective.
You should not take chloroquine or hydroxychloroquine while you are taking remdesivir. Either of these other medicines could make remdesivir less effective.
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A negative COVID-19 test does not mean recovery


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The American Society of Health-System Pharmacists, Inc. represents that the information provided in the accompanying monograph was formulated with a reasonable standard of care, and in conformity with professional standards in the field. Readers are cautioned that Remdesivir is not an approved treatment for coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2, but rather, is being investigated for and is currently available under an FDA emergency use authorization (EUA) for the treatment of severe COVID-19 in hospitalized patients.


Side effects include:

Randomized, double-blind, placebo-controlled trial in hospitalized adults with severe COVID-19 in China:
Adverse events (e.g., constipation, hypoalbuminemia, hypokalemia, anemia, thrombocytopenia, increased total bilirubin concentrations) reported in 66 or 64% of patients who received remdesivir or placebo, respectively.
Serious adverse events reported in 18 or 26%, respectively, and drug discontinued because of adverse events in 12 or 5%, respectively.
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Phase 3, adaptive, randomized, placebo-controlled trial in hospitalized adults with mild/moderate or severe COVID-19 (NCT04280705; ACTT-1): Serious adverse events (e.g., cardiac events, respiratory distress or failure, acute kidney injury, hypotension) reported in 21% in remdesivir group and 27% in placebo group; grade 3 or 4 adverse events occurred in 29% in remdesivir group and 33% in placebo group.
Most common nonserious grade 3 or greater adverse events in remdesivir group were anemia or decreased hemoglobin concentrations (8%); acute kidney injury, decreased eGFR or Clcr, or increased Scr (7%); pyrexia (5%); hyperglycemia or increased blood glucose concentrations (4%); and increased ALT and/or AST concentrations (4%); these were reported in 3–9% of patients in placebo group.
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Phase 3, randomized, open-label trial in hospitalized adults with severe COVID-19 (NCT04292899; GS-US-540-5773; SIMPLE-Severe): Adverse events reported in 70 or 74% of patients who received a 5- or 10-day remdesivir regimen, respectively; serious adverse events (e.g., respiratory distress or failure, septic shock) reported in 21 or 35%, respectively, and grade 3 or greater adverse events reported in 30 or 43%, respectively.
Drug discontinued because of adverse events in 4% of patients in 5-day group and 10% of patients in 10-day group. All-cause mortality at day 28 was 10 or 13% in the 5- or 10-day group, respectively.
Most common adverse events overall were nausea (10 or 9%), acute respiratory failure (6 or 11%), increased ALT concentrations (6 or 8%), and constipation (7% in both groups),

Cohort of 53 hospitalized patients in manufacturer's compassionate-use program: Adverse events (e.g., increased hepatic enzymes, diarrhea, rash, renal impairment, hypotension) reported in 60% of patients; serious adverse events (e.g., multiple organ dysfunction syndrome, septic shock, acute kidney injury, hypotension) reported in 23%; drug discontinued because of adverse events in 8% of patients.
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What Patients are being told
( CHINA SHARED their RESULTS.. above ) This is what is being shared in this country.


.

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The FDA has authorized emergency use of remdesivir only in people with COVID-19 who are in a hospital.
You must remain under the care of a doctor while receiving remdesivir.

Remdesivir side effects
Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Some side effects may occur during the injection. Tell your caregiver right away if you have:
  • nausea, vomiting;
  • chills or shivering;
  • increased sweating; or
  • a light-headed feeling, like you might pass out;
Common side effects may include:
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
 

Fine1952

The Age of Aquarius
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Sep 27, 2005
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Healthcare Provider
He has heart trouble and he is obese---both of these pre existing conditions do not work well in his favor regarding this manmade virus.
 

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