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Umbralisib (Ukoniq): Drug recall because increased risk of patient death
Genetic links revealed between severe COVID-19 and other diseases
SARS-CoV-2 Delta Variant: Resistance Mutations after Sotrovimab Use
Genetic variations and social health determinants may lead to higher risk for diabetes in individuals with high African heritage
AGMP: The African Genomic Medicine Portal
Genetic variants in extremely ill COVID patients explain how fatally sick people may get
What do genes tell about black coffee and chocolate?
Drivers of severe Covid-19 disease in patients under 50 without comorbidities
SARS-CoV-2-like RBD allowing ACE2-mediated entry into human cells from bats of Indochinese peninsula
Coronavirus epidemics first hit more than 21’000 years ago
Study of East Africans illuminates new genetic factors underlying human faces
Extracts from Artemisia annua active in vitro against SARS-CoV-2
Genetic susceptibility and severity loci for Covid-19 disease
Serious adverse events after Covid-19 vaccination occur but are very rare
Fish oil: Your genotype may tell you to take it or not

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FDA press releases

FDA Flexibilities to Yield Millions of Cans of Additional Infant Formula in Coming Months to Increase Supply Available to U.S. Consumers May 24, 2022
FDA Roundup: May 24, 2022 May 24, 2022
FDA Approves First Treatment for Eosinophilic Esophagitis, a Chronic Immune Disorder May 20, 2022
FDA Roundup: May 20, 2022 May 20, 2022
FDA Urges Drug Manufacturers to Develop Risk Management Plans to Promote a Stronger, Resilient Drug Supply Chain May 19, 2022

FDA MedWatch

Abbott Medical Recalls Dragonfly OpStar Imaging Catheter for Potential Loose Catheter Marker Band That May Cause Patient Harm May 26, 2022
2022 Medical Device Recalls May 26, 2022
Urgent Voluntary Recall: CorneaGen Cornea/ Cornea Patch Grafts; CorneaGen is voluntarily recalling Corneal Patch Grafts bearing the following product numbers: W419221004861104; W419221004861105; W419221004861106; W419221004861103 May 25, 2022
2022 Biologics Recalls May 25, 2022
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure May 23, 2022

EMA Press releases

Hydroxyethyl-starch solutions for infusion recommended for suspension from the market, CMDh, 25/02/2022 May 25, 2022
EMA business hours over Ascension Day holidays, 26 and 27 May, , 24/05/2022 May 24, 2022
EMA guidance supports development of new antibiotics, , 24/05/2022 May 24, 2022
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 16-19 May 2022, CHMP, 20/05/2022 May 20, 2022
First therapy to treat two types of Niemann-Pick disease, a rare genetic metabolic disorder, CHMP, 20/05/2022 May 20, 2022

random genetics

Treatment for myelodysplastic syndrome by hypomethylating agents may activate an oncogene May 26, 2022
Hypomethylating agents (HMA) are currently used as a first-line treatment for patients with myelodysplastic syndrome (MDS), and increasingly in other diseases, but their mechanism of action is not clear. HMAs may affect many genes and could potentially activate an oncogene—a gene that contributes to the development of cancer—but this has not been clearly demonstrated to […]
Study reveals cause, potential precision therapies for aggressive lymphoma May 25, 2022
DNA mutations are essential to the rapid development of an array of antibody-producing immune cells called B cells that collectively can recognize a vast number of specific targets. But this process can go awry in people with a mutation in a gene called SETD2, leading to a type of aggressive blood cancer, according to a […]
New study looks at heart defect risk in children of people with heart defects May 25, 2022
Congenital heart defects may be much more common among children of women with heart defects than of men with heart defects, according to new research.
How a genetic mutation affects the body's immune system response to viruses, development of blood cancers May 25, 2022
The body's innate immune system, active from birth, is the first line of defense against viruses and other pathogens that cause disease. Using vaccination as an example, after receiving a vaccine, pain, redness, or swelling may occur at the injection site. This response is a demonstration of how the immune system is turned on, but […]
New method for diagnosing chromosome errors May 25, 2022
The most common cause of spontaneous abortions is chromosome defects, but they can be difficult to detect. Researchers from the University of Copenhagen have developed a new method that can make us wiser about how chromosome defects and disease-associated chromosome changes look and how to aid diagnosis.

thasso

thasso, the new generation glocalized patient network in theragenomic and personalized medicine and individualized drug safety provides access to and sharing of personal and professional information in health and disease to individual patients, to patient subgroups, and to large patient populations worldwide

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Social Media, Social Network, Theragenomic Medicine, Social Medicine, Personalized Medicine, Genomic Medicine, Participative Medicine, Targeted Therapy, Individualized Therapy, Personalized Therapy, Individualized Drug Safety, Personalized Drug Safety, Genetic Variants, Allelic Variants, Genotypes, Molecular Phenotypes, Clinical Phenotypes, Companion Test, Heart Disease, Arthritis, Asthma, Diabetes, Hypertension, Malignant Tumors, Breast Cancer, Lung Cancer, Skin Cancer, Erectile Dysfunction, Crowd Sourcing, Patient Sourcing, Participative Sourcing, Collective Experience, Collective Community Wisdom, Apomediary Patient Expert, Patient Cloud,