STAT

STAT+: How to ‘break the logjam’? Economists pitch a plan to curb dire drug shortages

There are alarmingly frequent reports of shortages of vitally needed medicines. From tablets to treat ADHD and severe pain to injectable treatments for syphilis and various cancers, the U.S. has been facing a number of serious shortages recently. And this was before a U.S. Senate report found the number of active shortages reached a peak at 295 at the end of 2022.

The reasons can vary, from quality control failures at manufacturing plants to surging demand, including significant interest that has at times squelched availability of drugs taken for weight loss.

But the problem is not easily fixed. Most active pharmaceutical ingredients are made in China, and boosting production in the U.S. is not like flipping a switch. Many of the drugs in short supply are generics made in India, where regulators often find serious production lapses. So what to do? Along with a colleague, Marta Wosińska, a senior fellow in economic studies at The Brookings Institution, has three ideas to alleviate shortages of generic sterile injectable medicines, in particular. They suggest the U.S. government should provide incentives to upgrade facilities and create a buffer inventory. But they also argue hospital purchasing is in need of an overhaul. We discussed the possibilities; our conversation has been lightly edited. 

I’ve been writing about drug shortages on and off for many years, but the problem never goes away. And now, it seems even worse. Obviously, something has to change. But what exactly has been lacking with our policies to date?

Continue to STAT+ to read the full story…

1 year 9 months ago

Pharma, Pharmalot, Biotech, Cancer, Pharmaceuticals, STAT+

Medical News, Health News Latest, Medical News Today - Medical Dialogues |

Takeda voluntary withdraws US Biologics License Application for Dengue vaccine

Takeda's tetravalent dengue vaccine candidate (TAK-003) is based on a live-attenuated dengue serotype 2 virus, which provides the genetic “backbone” for all four vaccine viruses

Takeda's tetravalent dengue vaccine candidate (TAK-003) is based on a live-attenuated dengue serotype 2 virus, which provides the genetic “backbone” for all four vaccine viruses

Osaka: Takeda has announced that the Company has voluntarily withdrawn the U.S. Biologics License Application (BLA) for its dengue vaccine candidate, TAK-003, following discussions with the U.S. Food and Drug Administration (FDA) on aspects of data collection, which cannot be addressed within the current BLA review cycle.

The future plan for TAK-003 in the U.S. will be further evaluated given the need for travelers and those living in dengue-endemic areas of the U.S., such as Puerto Rico. The vaccine is approved in multiple endemic and non-endemic countries, with more approvals expected over the coming years.

“Our clinical program was designed to account for the complex global nature of dengue, and data from our 4.5-year trial has built confidence in TAK-003’s ability to help provide long-term protection against dengue, with a positive benefit and risk profile regardless of baseline serostatus,” said Gary Dubin, M.D., president of Takeda’s Vaccines Business Unit. “The urgent global need to combat the growing burden of dengue remains, and we will continue to progress regulatory reviews and provide access for people living in and traveling to dengue-endemic areas while we work to determine next steps in the U.S.”

The efficacy and safety profiles of TAK-003 have been demonstrated through a robust clinical trial program, including a 4.5-year Phase 3 study of over 20,000 children and adolescents living in eight dengue endemic areas. The study was designed per World Health Organization (WHO) guidance for a second-generation dengue vaccine, and it considered the need to achieve high levels of subject retention and protocol compliance in endemic regions.

Last year, TAK-003 received a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) after going through the EU-M4all process, a parallel review of the vaccine for use in the EU and participating dengue endemic countries around the world. The vaccine has since been approved in the EU, United Kingdom, Brazil, Argentina, Indonesia, and Thailand.

Dengue is a global public health crisis and further prevention measures are needed to support the millions of individuals around the world exposed to dengue.

Takeda's tetravalent dengue vaccine candidate (TAK-003) is based on a live-attenuated dengue serotype 2 virus, which provides the genetic “backbone” for all four vaccine viruses.

Read also: Taked Dengue Tetravalent Vaccine QDENGA gets European Commission nod

1 year 9 months ago

News,Industry,Pharma News,Latest Industry News

Medical News, Health News Latest, Medical News Today - Medical Dialogues |

Lupin Pithampur Unit-2 facility gets EIR from USFDA

Mumbai: Global pharma major Lupin Limited has announced that the company has received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (U.S. FDA) for its Pithampur Unit-2 manufacturing facility that manufactures oral solids and ophthalmic dosage forms.

The EIR was issued post the last inspection of the facility conducted from March 21 to March 29, 2023. The U.S. FDA has determined that the inspection classification of the facility is Voluntary Action Indicated (VAI).

VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.

“We are pleased to have received the EIR from the US FDA with a satisfactory VAI status for our Pithampur Unit-2 facility. This is a significant milestone as we build back our reputation of being best-in-class in Quality and Compliance. We look forward to new products approvals and launches, especially ophthalmic products from this facility now,” said Nilesh Gupta, Managing Director, Lupin.

Read also: USFDA inspection: Lupin gets 10 observations for Pithampur facility

Lupin is an innovation-led transnational pharmaceutical company headquartered in Mumbai, India. The Company develops and commercializes a wide range of branded and generic formulations, biotechnology products, and APIs in over 100 markets in the U.S., India, South Africa, and across the Asia Pacific (APAC), Latin America (LATAM), Europe, and Middle East regions.

Read also: Lupin CSR arm, Maharashtra Govt collaborate to address growing prevalence of cardiovascular diseases, COPD

The Company specializes in the cardiovascular, anti-diabetic, and respiratory segments and has a significant presence in the anti-infective, gastro-intestinal (GI), central nervous system (CNS), and women’s health areas. The company invested 7.9% of its revenue in research and development in FY23.

Lupin has 15 manufacturing sites, 7 research centers, and has been consistently recognized as a ‘Great Place to Work’ in the Biotechnology & Pharmaceuticals sector.

Read also: Lupin gets USD 25 million from AbbVie for novel MALT1 inhibitor program to treat hematological cancers

1 year 9 months ago

News,Industry,Pharma News,Latest Industry News

Health

Men, fix your low sperm count!

A LOW sperm count, also called oligozoospermia, is where a man has fewer than 15 million sperm per millilitre of semen. Normal sperm densities range from 15 million to greater than 200 million sperm per millilitre of semen. You are considered to...

A LOW sperm count, also called oligozoospermia, is where a man has fewer than 15 million sperm per millilitre of semen. Normal sperm densities range from 15 million to greater than 200 million sperm per millilitre of semen. You are considered to...

1 year 9 months ago

Health

The importance of ital food in our culture

ITAL SIMPLY means natural! It is not just a cuisine, but a lifestyle based on the Rastafarian faith, which is well known in Jamaica and other parts of the Caribbean. Ital cuisine means no salt and no chemically modified additives. Ital has been...

ITAL SIMPLY means natural! It is not just a cuisine, but a lifestyle based on the Rastafarian faith, which is well known in Jamaica and other parts of the Caribbean. Ital cuisine means no salt and no chemically modified additives. Ital has been...

1 year 9 months ago

Health – Demerara Waves Online News- Guyana

Heart surgeons in Guyana use cow tissue to reconstruct patient’s heart

The Caribbean Heart Institute’s (CHI) team led by CEO and Guyanese born heart surgeon Dr. Gary Stephens, successfully conducted an open-heart surgery utilising cow tissue to reconstruct a patient’s heart, the institution said Tuesday. “This procedure is the first-ever open heart surgery of its kind, to be performed in the country,” CHI added. CHI explained ...

The Caribbean Heart Institute’s (CHI) team led by CEO and Guyanese born heart surgeon Dr. Gary Stephens, successfully conducted an open-heart surgery utilising cow tissue to reconstruct a patient’s heart, the institution said Tuesday. “This procedure is the first-ever open heart surgery of its kind, to be performed in the country,” CHI added. CHI explained ...

1 year 9 months ago

Health, News

PAHO/WHO | Pan American Health Organization

OPS y autoridades regulatorias de referencia regional buscan superar brechas para fortalecer la regulación de productos médicos en las Américas

PAHO and national regulatory authorities of regional reference seek to strengthen regulation of medical products in the Americas

Cristina Mitchell

11 Jul 2023

PAHO and national regulatory authorities of regional reference seek to strengthen regulation of medical products in the Americas

Cristina Mitchell

11 Jul 2023

1 year 9 months ago

Health – Demerara Waves Online News- Guyana

Guyana awaits word from US on catfish ban

Guyana is still awaiting a reply from the United States Department of Agriculture to several submissions aimed at having that North American country lift an almost six-year old ban on catfish, according to Agriculture Minister Zulfikar Mustapha. With Guyana having recently updated its previous submission, he said the Ministry of Agriculture was awaiting word from ...

Guyana is still awaiting a reply from the United States Department of Agriculture to several submissions aimed at having that North American country lift an almost six-year old ban on catfish, according to Agriculture Minister Zulfikar Mustapha. With Guyana having recently updated its previous submission, he said the Ministry of Agriculture was awaiting word from ...

1 year 9 months ago

Business, Health, News

Health – Dominican Today

Adolfo Pérez says the Abinader government has doubled the budget for high-cost medicines

Santo Domingo.- The director of the Central Logistics Support Essential Medicines Program (Promese Cal), Adolfo Pérez de León reported this Tuesday that it has been in the Government headed by President Luis Abinader where resources for the purchase of high-cost medicines have doubled.

Santo Domingo.- The director of the Central Logistics Support Essential Medicines Program (Promese Cal), Adolfo Pérez de León reported this Tuesday that it has been in the Government headed by President Luis Abinader where resources for the purchase of high-cost medicines have doubled.

During an interview in El Gobierno de la Mañana, the official added that said program has also tripled the number of patients who demand said medicines.

“The reality of the program is that it is being increased, in terms of patients and also strengthened in all its management capacity. It has been in this government of President Luis Abinader where the number of patients benefiting from the program has tripled and where the budget for the purchase of these drugs has doubled, ”he assured.

Adolfo Pérez explained that of some 5,729 active patients that the current administration found in 2020, there are currently more than 16,500 patients.

He affirmed that the high-cost drug program is well and supplied, for which a tender has been launched to continue the purchase of drugs for some 3,200 million pesos, to continue guaranteeing access to those in need.

The incumbent of Promese Cal stated that steps are being taken to integrate new patients into the program, and incidentally continue with the rate of help.

1 year 9 months ago

Health

Medscape Medical News Headlines

Cigna to Add 3 Humira Biosimilars to Drug Reimbursement List

Cigna Group's Express Scripts pharmacy benefits unit will add three biosimilar versions of AbbVie's blockbuster arthritis treatment Humira to its list of preferred drugs, the company said on Monday. Reuters Health Information

Cigna Group's Express Scripts pharmacy benefits unit will add three biosimilar versions of AbbVie's blockbuster arthritis treatment Humira to its list of preferred drugs, the company said on Monday. Reuters Health Information

1 year 9 months ago

Dermatology, News

STAT

STAT+: Pharmalittle: Eisai executive to retire; Express Scripts adds three Humira biosimilars to formulary

Top of the morning to you, and a fine one it is. Birds are chirping and cool breezes are wafting by the Pharmalot campus, where the official mascots are racing about the grounds. As for us, we are ensconced doing the usual sorts of things — updating our to-do list, brewing cups of stimulation (our choice today is chocolate raspberry) and foraging for items of interest.

Speaking of which, we have gathered the latest bushel for your perusal if you scroll down a wee bit. Of course, all of this means that it is time to get cracking. So here we go. We hope you have a smashing day and conquer the world. And as always, please do stay in touch …

Eisai announced that Ivan Cheung, who ran its global Alzheimer’s drug program, will retire at the end of the month and be replaced by the son of Eisai chief executive officer Haruo Naito, STAT writes. The move comes after Cheung led the push for U.S. approval of the breakthrough medicine Leqembi. Keisuke Naito, 34, a senior vice president and chief strategy and planning officer, will become acting global Alzheimer’s officer. Cheung’s resignation comes less than a week after Eisai and Biogen were granted full approval for Leqembi in the U.S. The drug is the first medicine shown to slow progression of the disease, which afflicts some 6 million Americans.

Express Scripts will add three biosimilar versions of AbbVie’s blockbuster arthritis treatment Humira to its list of preferred drugs, Reuters notes. The biosimilars include branded and unbranded versions from Sandoz, the generic unit of Novartis, as well as one from Boehringer Ingelheim. Express Scripts, the pharmacy benefits manager owned by Cigna, said the biosimilars would be included as preferred brands on its formulary. The drugs, launched this month, add to competition for Humira in the U.S. that started in January with the launch of a biosimilar by Amgen that is already on Express Scripts formulary.

Continue to STAT+ to read the full story…

1 year 9 months ago

Pharma, Pharmalot, Biosimilars, Pharmaceuticals, STAT+

Medical News, Health News Latest, Medical News Today - Medical Dialogues |

WBMCC invites Applications For Centralized Online Counselling of Sponsored DNB Seats, Check out details

West Bengal: The application for participation in centralized merit-based online counselling for admission to Sponsored DNB seats (Post MBBS and Post Diploma) 2023 is sought from the eligible candidates. The West Bengal Main Computerized Counselling (WBMCC) has released a detailed schedule.

All such candidates who fulfill the eligibility criteria and are desirous of opting for the sponsored DNB (Post MBBS and Post Diploma) seats 2023 are required to submit their application to the Director of Medical Education, Dept of Health and Family Welfare, Swasthya Bhawan, GN-29, Sector —V, Kolkata -700091. (If they belong to the WIIMES cadre) or Director of Health Services, Dept of Health and Family Welfare, Swasthya Bhawan, GN-29, Sector —V, Kolkata -700091(11 they belong to WBHS or WI3PIIAS cadre).

The submission of the application will be via email at tr.noc.mert@gmail.com for the candidates of WBHS and WBPHAS and via email at wbcounselingcell@gmail.com for the candidates of WBMES in the required format. The circular is already published on the websites www.wbhealth.gov.in and www.wbmcc.nic.in dated 22.3.2023. The applications will have to be submitted by 5:00 pm on 17.7.2023.

Eligibility criteria for Sponsored DNB (Post MBBS) seats –

1. Candidates who are working under the Dept of Health and Family Welfare Govt. of West Bengal on a regular basis are eligible for Sponsored DNB (Post MBBS) seats.

2. Candidates must be in possession of the M1313S degree Certificate recognized by the Indian Medical Council Act 1956 and possess a permanent registration certificate of MBBS qualification issued by the Medical Council of India/ State Medical Council.

3. Must have "Qualified" MEET PG 2023.

Also Read:TN Health Issues Clarification on eligibility for NEET PG, MDS candidates, check out details

Eligibility criteria for Sponsored DNB (Post Diploma) Seats -

1. Candidates who are working under Dept of Health and [Tamil) Welfare Govt. of West Bengal on a regular basis are eligible for Sponsored DNB (Post Diploma) seats.

2. Candidates who have passed the final examination leading to the award of Post Graduate Diploma from Indian Universities, which are duly recognized as per provisions of the Indian Medical Council Act 1956, Govt, of India i.e. have passed final examinations for Postgraduate diploma on or before 31-03-2021 as per provisions of the Trainee Reserve Rules 2015 and its amendments.

3. Candidate must have "Appeared" in DNB-PDCLT 2023.

The physical verification of the candidates shall be conducted from 12 noon till 3 pm on the days as follows: 17-07-2023 till 20-07-2023 (4 days). During such physical verification, the candidate has to attend with the original documents along with the filled-up and duly forwarded proforma as stated above and one set self-attested photocopies of the original documents before the Assistant Director of Medical Education at the Counseling Cell in the ground floor of Swasthya Sathi Building within premises of Swasthya Bhawan (for WBMES cadre) or Assistant Director of Health Services, MERT, in rd floor of B wing at Swasthya Bhawan (if they belong to WBVIS/WBPHAS cadre).

The following documents are required to be placed for verification (original and one set self-attested photocopy) -

1. MEET PG 2023/DNB PDCET 2023 --rank card and admit card

2. Any two of the following valid photo ID (Aadhar card/Voter card/Passport)

3. Age proof (birth certificate/class X admit card/class X certificate)

4. MBBS certificate and final rvIBBS mark sheet

5. Permanent Registration certificate issued by MCIINMC/WBMC

6. Caste certificate (as applicable and issued by the appropriate authority in West Bengal)

7. Non-creamy layer certificate for OBC candidates issued on or after 01.04.2023

8. PwD certificate (as applicable and issued by Medical Board of IPGMER Kolkata)

9. Proof of previous Diploma if acquired (on or before 31.03.2021)

10. Proof of any bond formalities (if applicable, to be completed on or before 31.03.2023)

11. Posting orders and joining reports as proof of regular service

The candidates who fail to submit email on time or fail during verification, or do not attend verification with required documents within the scheduled time, shall not be included in the list for provisional NOC (No Objection Certificate) for Centralized merit-based online counseling for admission to Sponsored DNB seats (Post MBBS and Post Diploma) 2023.

The provisionally eligible candidates shall be handed Provisional NOC on authenticated letterhead, and the scanned copy shall be uploaded to the websites www.wbhealth.gov.in and www.wbmcc.nic.in for public viewing on or after 29.07.2023. It shall also be communicated to NBEMS as per their instructions via email req.cc@natboard.edu.in latest by 31.07.2023. The format of NOC shall be provided by NBEMS in their notice 04.07.2023 on the website www.natboard.edu.in.

The candidates shall bear in mind that this NOC is purely provisional and does not ensure a seal for a particular candidate. The in-service candidates of the Dept. of Health and Family Welfare, Government of West Bengal, must contact respective branch officials to find out whether they are eligible for trainee reserve as per extant rules so that seats are not wasted after allotment, if any.

To view the notice, click on the link below –

https://medicaldialogues.in/pdf_upload/dnb-214034.pdf

Also Read:BFUHS Allocates 95 Seats For BSc Paramedical Courses, Check out Counselling Schedule

1 year 9 months ago

State News,News,West Bengal,Medical Education,Medical Admission News,Latest Medical Education News

Health News Today on Fox News

Be well: Recognize the warning signs of ‘dry drowning’ and take quick action

Every year, there are some 4,000 fatal drownings and 8,000 nonfatal drownings in the U.S., per the Centers for Disease Control and Prevention (CDC) — and not all of them meet the textbook definition.

Even if a child appears to be "safe" after a water incident, the child could still be in danger if even a small amount of water has entered the lungs.

Every year, there are some 4,000 fatal drownings and 8,000 nonfatal drownings in the U.S., per the Centers for Disease Control and Prevention (CDC) — and not all of them meet the textbook definition.

Even if a child appears to be "safe" after a water incident, the child could still be in danger if even a small amount of water has entered the lungs.

Unofficially known as "dry drowning," this condition can cause inflammation or swelling and make it difficult to breathe even after a child is out of the water, according to Dr. Denise Scott, a pediatrician who is co-founder of Oklahoma City’s first after-hours pediatric urgent care clinic. 

BE WELL: PREVENT DROWNING WITH THESE CHILD WATER SAFETY TIPS

"While ‘dry drowning’ is actually not a medical term or diagnosis, it does describe a condition that is a complication of a water event, termed ‘post-immersion syndrome,’" Scott told Fox News Digital.

"Post-immersion syndrome, considered a nonfatal drowning, describes an event in which a person was submersed in water but the lungs were not filled with water (thus dry)."

When this occurs, water has been inhaled — not swallowed — through the nose or mouth. 

"Water in the airways can lead to laryngospasm, or vocal cord spasm, making it difficult to breathe," explained Scott, who also works on the JustAnswer.com platform fielding questions about a wide variety of children’s health issues

"This makes it difficult to get air into the lungs."

CONTAMINATED BEACH WATER COULD MAKE SWIMMERS SICK, WARNS NEW POLLUTION REPORT: ‘SEVERAL TROUBLING TRENDS’

Post-immersion syndrome can occur after anyone has been in any body of water, whether it’s a lake, swimming pool, bathtub or hot tub.

"Technically, any drowning is the result of not getting air in the lungs, whether the lungs are wet or dry," Scott said. 

The most obvious sign of post-immersion syndrome is excessive or continuous coughing, Scott said.

"If someone inhales water, their response is to cough, which often expels the water," the doctor said. "The concern is when the cough continues after an episode of 30 to 60 minutes or longer."

Other warning signs that occur immediately after an episode or within an hour include difficulty breathing or speaking, rapid and hard breathing, chest pain, wheezing or vomiting.

Later symptoms, usually within two to three hours, can include confusion, sleepiness, and continued coughing and breathing difficulties, all of which can be signs of decreased oxygen, said Scott.

"A child who has either been rescued from water or inhaled water and has any of the above symptoms should be taken in for a medical evaluation," Scott said. "For any child who is not breathing, CPR should be given and 911 should be called."

A child with symptoms of post-immersion syndrome usually will be observed at the hospital for up to eight hours before the physician decides whether to pursue further treatment, Scott said.

SUMMER MELTDOWNS: HERE'S HOW EXTREME HEAT CAN AFFECT YOUR MOOD AND MENTAL HEALTH

"Keeping a child calm can sometimes help the muscle spasms to relax," she added.

Although this condition is uncommon, it can be fatal if symptoms aren't addressed and lack of oxygen occurs, the doctor said. 

"A severe laryngospasm that isn't relieved ultimately can lead to lack of oxygen and cardiac arrest," she warned. "Long-term effects are the result of poor oxygen to any organ system, especially the brain, which can result in seizures or brain damage."

Drowning is the most common cause of unintentional death in children between ages 1 and 4 and the second leading cause of death in children between ages 5 and 14, per the CDC. 

Most drownings are preventable. 

"First and foremost, children should never swim unsupervised or alone," Scott said. 

"Young children who cannot swim should have an adult within arm's reach and wear a personal flotation device."

Private swimming pools should have a fence around them to prevent someone from wandering in, she went on. Children should always wear life vests when they're near or around lakes. 

CLICK HERE TO SIGN UP FOR OUR HEALTH NEWSLETTER

While it’s a good idea to have young children take swim lessons, Scott emphasized that it is not a safeguard, nor should it give a false sense of security or take the place of close adult supervision.

Parents also should learn CPR, she added.

While post-immersion syndrome can happen to someone at any age, children are at the greatest risk, Scott said.

"Adults and teens are more likely to be at risk if they go swimming after consuming alcohol, but anyone can accidentally inhale water when submersed," she said. 

"The vast majority of the time, this clears up with coughing. For persistent symptoms, one should seek medical care."

1 year 9 months ago

Health, childrens-health, be-well, health-care, lifestyle, respiratory-health

PAHO/WHO | Pan American Health Organization

PAHO convenes health and foreign affairs authorities for second meeting on future pandemic agreement

PAHO convenes health and foreign affairs authorities for second meeting on future pandemic agreement

Cristina Mitchell

10 Jul 2023

PAHO convenes health and foreign affairs authorities for second meeting on future pandemic agreement

Cristina Mitchell

10 Jul 2023

1 year 9 months ago

Health | NOW Grenada

Joining hands to eliminate litter and Dengue fever

“By collectively adopting these preventive measures, we can significantly reduce the risk of Dengue fever transmission and protect our communities’ health and well-being”

1 year 9 months ago

Health, PRESS RELEASE, dengue, grenada green group, mosquito

Medical News, Health News Latest, Medical News Today - Medical Dialogues |

MCC issues notice on BSc Nursing Counselling Process For Colleges Affiliated To IP University, Check out details

Delhi: Medical Counselling Committee (MCC) has issued a notice related to BSc Nursing counselling process for the college affiliated to IP University.

As per the notice, the counselling process of the BSc(H) Nursing program 2023-24 for the following colleges affiliated to IP University will be conducted by the university itself and not by MCC, in reference to Notification no. 30/2023 dated 28.06.2023 issued by GGSIPU.

1. Lakshmi Bai Batra, College of Nursing

2. St. Stephen’s College of Nursing, Tis Hazari, Delhi (Christian Minority)

3. College of Nursing, Hindu Rao Hospital

4. College of Nursing, Kasturba Hospital

5. Panna Dai, College of Nursing, DDU

6. Shakuntala Devi College of Nursing

Also Read:GGSIPU Extends deadline For Registration, Fee Payment, Documents Verification For MBBS, BSc Nursing admissions

However, the counselling for B.Sc(Nursing) courses for the Nursing colleges of VMMC & Safdarjung Hospital and Dr RML Hospital will be conducted by the Medical Counselling Committee of DGHS as done in the previous year along with the following nursing colleges.

1. College of Nursing Florence Nightingale CON, New Delhi

2. College of Nursing LHMC, New Delhi

3. College of Nursing RAK CON, New Delhi, Rajkumari Amrit Kaur College of Nursing

4. College of Nursing Bhopal Nursing College, BMHRC, BHOPAL, Bhopal Memorial Hospital and Research Centre

5. College of Nursing BHU, VARANASI

Bsc Nursing counselling process by IP University:

Documents verification –

Online verification of documents by the University

Closing Date MBBS, BSc Nursing

The candidate claiming benefits under the reserved category has to upload the relevant supporting documents duly issued by Competent Authority.

The candidates may kindly read Admission Brochure to see the details of documents required for being eligible to claim benefits under the Reserved Category and for the ARMY category, please upload Appendix 9(A)/9(B)/9(C) of the Admission Brochure 2023-24.

10.07.2023 (11:50 PM

The candidates note that University's Verifying Officer shall raise queries in cases where the document(s) is deficient or any discrepancy is observed. Candidates are advised to revert back/ upload the required documents immediately to claim the benefit of the reserved category on merit.

The online registration and submission of counselling participation fees for admission in program MBBS and BSc (Hons) Nursing based on the merit of NEET UG 2023 will be in respect of the following medical colleges/institutes affiliated with Guru Gobind Singh Indraprastha University, New Delhi -

MBBS -

1. North DMC Medical College & Hindu Rao Hospital — NDMC (MC), Hindu Rao Hospital, Malkaganj, New Delhi (Admissions to be made against 85% State Quota seats only in respect of candidates who have completed their 11th & 12th class from any school located in the NCT of Delhi).

2. Dr. Baba Saheb Ambedkar Medical College and Hospital, Sector 6, Rohini, Delhi (Admissions to be made against 85% State Quota seats only in respect of candidates who have completed their 11th & 12th class from any school located in the NCT of Delhi)

3. Army College of Medical Sciences, Near Base Hospital, Delhi Gantt., New Delhi (Admissions to be made against 100% sanctioned intake). The admission to the ALMS i.e. Army College of Medical Sciences, is for the children of eligible serving Army personnel, Ex-Army personnel, and war widows/widows of the Army. The children of categories of Army personnel as detailed in Chapter 7. I .4 of the Admission Brochure 2022-23 are eligible, and they are required to upload the relevant certificate Appendix 9 (A), 9(B), 9(C) & 9 (D) as given against the category applicable to them as proof of their eligibility for admission to ALMS.

All the concerned candidates/stakeholders are hereby informed that the admission of 100% seats in the MBBS program at VMMC & Safdadung Hospital, New Delhi, and ABVIMS, Dr. RML Hospital, will be conducted by the Medical Counselling Committee, DGHS. Hence, whosoever is desirous of seeking admission to these 02 affiliated medical colleges/institutes may apply on the website of MCC, DGHS. (https://mcc.nic.in).

BSC (Hons) Nursing –

1. Lakshmi Bai Batra College Of Nursing

2. St. Stephen's College Of Nursing, Tis Hazari, Delhi (Christian Minority)

3. College of Nursing Hindu Rao Hospital

4. College of Nursing Kasturba Hospital

5. Panna Dai College of Nursing, DDU

6. Shakuntala Devi College or Nursing

All the concerned applicants/stakeholders are hereby informed that the admission of 1 00% seats in the BSc (Hons) Nursing program at the College of Nursing, Safdariung Hospital, New Delhi, and College of Nursing. The Medical Counselling Committee, DGHS, will conduct Dr. RML Hospital. Hence, whosoever is desirous of seeking admission to these 02 affiliated medical colleges/institutes may apply on the website of MCC. DGHS. (https://mcc.nic.in).

Eligibility criteria

BSC (Hons) Nursing -

All candidates must appear in the National Eligibility cum Entrance Test — Undergraduate of 2023 (NEET UG 2023) and qualify to be considered for admissions.

Admission terms and conditions -

The minimum qualifying criteria for entrance test to admission to BSc Nursing is as under –

1. General 50th Percentile

2. SC/ST/OBC 40th Percentile

3. General-PwD 45th Percentile

4. SC/ST/OBC-PwD 40th percentile

5. Regarding candidates belonging to SC/ST/OBC, the marks obtained in 3 subjects, Physics, Chemistry, and Biology, shall be 40% individually.

MBBS -

1. Candidate should be an Indian/ Overseas Indian / Nepal citizen. Non-Resident Indians and Foreign Nationals are not eligible.

2. The candidate should be medically fit to pursue the allocated course on medical examination.

3. The candidate should have attained the age of 17 years on or before 31' December of the year of his/her admission to the first year of the Course.

4. No provisional admission will be done for any result awaited or Compartment / Supplementary cases. The admission to the ACMS i.e. Army College of Medical Sciences, is for the children of eligible serving Army personnel, Ex-Army personnel, and war widows/widows of the Army. The children of categories of Army personnel, as detailed in chapter 7.1.4 of the Admission Brochure 2022-23, are eligible. They are required to upload the relevant certificate Appendix 9 (A), 9(B), 9(C) & 9 (D) as given against the category applicable to them as proof of their eligibility for admission to ACMS.

The candidate seeking admission under reserved categories has to mandatorily upload the entitled supporting certificate in his/her name. The Candidates, for further details, must read Chapter 6 (Reservation Policy) of the respective Admission Brochure 2023-24.

In case the candidate is claiming the seat reserved for DSC/DST/DOBC (wherever applicable) category, then He/ She should have passed his/ her qualifying exam from Delhi School/College and must have an SC/ST/OBC certificate issued by the Competent Authority of Govt. of NCT of Delhi only.

Reservation in OBC Category is not applicable for Master's Level and Postgraduate Diploma programs. The OBC category reservation applies only to the University School of Studies and Govt. Colleges (affiliated with GGSIPU) only.

For claiming reservation against the OBC category in Delhi Region, the candidate has to upload a valid OBC category certificate issued by a Competent Authority of Delhi in accordance with the list of OBC categories as per Govt. of NCT of Delhi. And suppose the OBC certificate is issued before 31.03.2023. In that case, it is mandatory for candidates to upload the OBC Non-Creamy Layer certificate, which should be issued after 31st March 2023 with the OBC certificate.

The EWS category reservation applies only to the University School of Studies and Govt. affiliated Colleges. This will be implemented in accordance with the Govt. of India and Govt. of NCT of Delhi orders as applicable. EWS Certificate should be issued after 31st March 2023 stating valid for year 2023-2024.

For claiming a reservation on a seat reserved for DEFENCE Category, the candidate must upload the duly filled and signed Appendix 1 of Admission Brochure 2023-24 issued by the competent authority as mentioned in Admission Brochure 2023-24 along with supporting documents. Reserved Category Candidates who fail to upload documents as per notified schedule or whose documents are not in order will forfeit his/her right to the reserved category claimed and will automatically be converted to General Category as per University rules.

For MBBS only: Candidates claiming a seat in the "Delhi Region" must have passed the qualifying examination (i.e. 11th and 12th ) from any institutes/ Colleges located in Delhi. Allotment of seats in the wrong region on account of incorrect filling of form will lead to cancellation of the allotment at any later stage, and the candidate will automatically lose the right to the seat in his bonafide region if not available at the time of cancellation of seat.

For BSc (Hons) Nursing - Candidates claiming seats in the "Delhi Region" must have passed the qualifying examination from any institutes! Colleges located in Delhi. Allotment of seats in the wrong region on account of incorrect filling of form will lead to cancellation of the allotment at any later stage. The candidate will automatically lose the right to the seat in his bonafide region if not available at the time of cancellation of the seat.

The registration process and counseling fee -

The candidates who have qualified for NEET UG 2023 and have filled online registration form of GGSIPU earlier, and have paid the Non-Refundable Registration Fee of Rs. 1500, such candidates are required to enroll for a centralized online counselling participation fee of Rs 1000 (non – refundable) through Net Banking/Debit Card/Credit Card. The last date to pay was 6.7.2023 up to 11.50 pm.

The candidates who have qualified for NEET UG 2023 and have not filled online registration form of GGSIPU earlier and have not paid the Non-Refundable Registration Fee of Rs. 1500, such candidates are required to register and pay the registration fee of Rs 1500 online and subsequently required to enrol for a centralized online counseling participation fee of Rs 1000 (non – refundable) through Net Banking/Debit Card/Credit Card. The last date to pay was 6.7.2023 up to 11.50 pm.

To view the notice, click on the link below –

https://medicaldialogues.in/pdf_upload/nursing-213866.pdf

Also Read:JIPMER To Conduct 1st Year PG Orientation Program From 19th To 21st July

1 year 9 months ago

State News,News,Delhi,Medical Education,Nursing education News,Latest Medical Education News

STAT

STAT+: The new weight loss drugs are revolutionizing our understanding of desire. Food cravings could be just the beginning

One month it was pizza. Starting in the late afternoon, while he was teaching a chem lab or grading student work, a part of Anthony Fernandez’s brain would stray to visions of steaming pies. The thought of sinking his teeth into one would tug at him as he packed up his things and walked to his car.

By the time he pulled out of the Merrimack College campus, the urge would become a tractor beam, reeling him into the small shop just shy of Route 125 for a slice or three.

It would go on like that for weeks. Intrusive phantom wafts of bubbling hot cheese seeping into his psychic space. An unwelcome rush of saliva. A pizza-shaped itch begging to be scratched. Then suddenly they would be gone. Replaced by a new fixation: coconut jelly sticks from Heav’nly Donuts one month, Dunkin’s Beyond Sausage sandwich the next.

Fernandez knew it was these roving food obsessions that were losing him his latest weight loss battle. The 53-year-old chemistry professor had been hovering between 275 and 295 pounds for most of his adult life. At 5’10”, that made him obese by most body mass index calculations. Then during the first year of the Covid-19 pandemic, while much of the rest of the country struggled with the “quarantine 15,” Fernandez shed 20 pounds while hunkering at his Massachusetts home. When he lost easy access to fast food, the weight followed.

But as stores and restaurants began to open up again, the numbers on his scale crept steadily higher. So did the number of fatty acids and excess sugar in his blood. Around Thanksgiving 2021, Fernandez’s doctor approached him about trying something different: a new weight loss drug called Wegovy.

Originally developed for people with type 2 diabetes like Fernandez’s parents, Wegovy — the brand name for one of an expanding class of injectable medicines known as GLP-1 receptor agonists — was helping people lose up to 15% of their body weight. The needles initially made him hesitate. But by late February last year, Fernandez came around to the idea. The first time he tried Wegovy, he made his wife stand next to him just in case he fainted. But the pen hid the needle from sight and he barely felt it pierce his skin. By the end of that first month, his urges had evaporated.

“From the get-go, I stopped having a lot of those in-between meal cravings,” Fernandez said. “I don’t find that I need those snacks in the middle of the day or late at night. I used to need something after I put the kids to bed. I’d pull out a bag of carrots and a jar of hummus and eat the whole damn thing. I don’t do that anymore.”

Fernandez is among an exploding number of Americans taking these drugs for weight loss — more than 5 million people in the U.S. were prescribed a GLP-1 agonist in 2022, up from about 230,000 in 2019, according to a recent analysis by data insights company Komodo Health. Their rapid adoption is a testament to their striking effectiveness — unmatched by any weight loss drugs in history. But even scientists who’ve spent decades dissecting the actions of the gut hormone these medicines are designed to mimic have been surprised by their potency.

GLP-1 was first identified more than 40 years ago as a chemical messenger produced in the gut that tells the pancreas to crank out more insulin. Scientists learned pretty quickly that it does so by binding to GLP-1 receptors dotting the surface of beta cells in the pancreas. But only in recent years have researchers begun to understand the extent to which the brain also uses GLP-1 as a signaling molecule. It’s through networks of neurons coated with GLP-1 receptors that GLP-1 agonists act to suppress eating — not only, as was long believed, by communicating feelings of fullness, but also by altering circuits in the brain that drive desire.

This wasn’t obvious back when these drugs were beginning to be developed. They weren’t, originally, even designed to get into the brain. But more and more, scientists are learning that’s where they work to cause weight loss. These revelations have the potential to lead to more potent versions of these drugs in the future. They also raise an even more tantalizing question: If hormone hacking can erase food cravings, what other destructive desires might it liberate us from one day?

Continue to STAT+ to read the full story…

1 year 9 months ago

In the Lab, The Obesity Revolution, addiction, neuroscience, Obesity, STAT+

Jamaica Observer

Diabetes and heart disease

Diabetes
particularly type 2 diabetes has been increasing in prevalence worldwide. In Jamaica 11.9 per cent of our population above the age of 15 have a diagnosis of diabetes. Diabetes increases the risk of heart disease, and cardiovascular disease is the most common cause of death for the diabetic patient.

Diabetes
particularly type 2 diabetes has been increasing in prevalence worldwide. In Jamaica 11.9 per cent of our population above the age of 15 have a diagnosis of diabetes. Diabetes increases the risk of heart disease, and cardiovascular disease is the most common cause of death for the diabetic patient.

Diabetic patients have an increased risk of atherosclerotic disease (that is laying down cholesterol in arteries) and the risks of stroke, coronary artery disease/heart attacks and peripheral vascular disease are all increased in the diabetic population. In addition, diabetics have been shown to an increased risk of heart failure that is not related to atherosclerosis. Given these findings a diagnosis of diabetes suggests the need to find measures to ameliorate these risks. Early studies looking at the treatment of diabetes suggested that lowering of the blood sugar levels over time decreased the likelihood of some of the complications of diabetes. These included the risk of eye disease, kidney disease and nerve disease. Interestingly, these studies did not demonstrate a reduction in the risk of cardiac and vascular disease despite improved diabetic control. Studies found that treatment of hypertension and high cholesterol in the diabetic patient reduced the risk of developing heart disease and for many years this was the primary focus of risk reduction. However, over the past five to 10 years new medications to lower blood sugar have been shown to improve outcomes and to reduce the risk of heart disease.

The improvement in the efficacy of medications available for treatment of diabetes can be traced back to 2008 when the Food and Drug Administration (FDA) in the United States changed the criteria for the approval of medications for diabetes. Prior to this date, it was enough to show that a medication improved glucose control. The experience with rosiglitazone, a medication which effectively lowered blood sugar but at the cost of an increased risk of heart attack and worsening of heart failure, lead to a change in the way in which medications for diabetes were approved. After 2008 companies developing new medications for diabetes needed to show that medications not only lowered blood sugar but that they did not worsen cardiovascular morbidity and mortality. Several classes of medications have been approved under this new standard with the last two groups: the glucagon like peptide agonists (GLP1 agonists) and the sodium glucose co-transport 2 inhibitors (SGLT2 inhibitors) demonstrating the ability to significantly improve cardiac outcome in patients with diabetes.

Currently, physicians who are treating patients with diabetes have several modalities to improve cardiac and vascular outcomes including lifestyle measures, management of additional cardiac risk factors and the use of diabetic medications with the ability to reduce death and disability from cardiac and vascular disease.

Lifestyle measures

All diabetic and cardiac societies advise lifestyle measures for the general population as well as for those diagnosed with diabetes. There is good evidence to suggest that lifestyle measures can help prevent abnormal glucose handling in the body and thus reduce the likelihood of the development of diabetes. Lifestyle measures can also significantly reduce the incidence of associated conditions that worsen cardiac and vascular outcome in the diabetic patient as well as improving outcome in those diabetic patients with heart disease. Dietary measures and exercise have been shown to reduce the incidence of patients with abnormal blood sugars going on to develop type 2 diabetes. They also reduce the risk of hypertension, hyperlipidemia and obesity which increase cardiac risk in the diabetic patient. Studies have also suggested that in patients with established heart disease (including diabetics) diet and exercise can improve cardiac outcome.

Cigarette smoking is one of the most important causes of avoidable death worldwide and significantly worsens the risk of heart and vascular disease in the diabetic patient. From the point of view of the heart and blood vessels any amount of smoking (even second-hand smoke) serves as a spur to vessel damage and the laying down of cholesterol in arteries. Obesity is prevalent in the Jamaican population (55.5 per cent of Jamaican adults). Obesity not only increases the risk of type 2 diabetes itself, but also increases several cardiac risk factors and the incidence of heart disease including heart failure and coronary artery disease. Good sleep hygiene, avoiding/limiting alcohol, not using illicit drugs and stress management all play important roles in improving long term cardiac and vascular outcome in all populations including diabetics.

Treatment of hypertension in diabetes

Hypertension and Diabetes (particularly Type 2 diabetes) frequently coexist. They have several risk factors in common including obesity, inactive lifestyle, family history etc. They also have several shared hormonal and metabolic abnormalities. Hypertension is twice as common in the diabetic population as compared to the general population. Hypertension and type 2 diabetes together increase the risk of increase heart enlargement, stroke and heart failure more than either condition alone. Many studies have demonstrated the importance of treating hypertension to reduce risk, with greater benefits being noted in the population with type 2 diabetes. One study found that lowering the systolic blood pressure by an average of 5.6mmHg lowered the risk of cardiovascular death by 18 per cent. A large meta-analysis of studies including approximately 79000 patients found that lowering the systolic blood pressure to less than 130 mmHg lowered the risk of stroke by 39 per cent. Evidence has been found that treating hypertension in diabetic patients lowers the risk of severe kidney disease, heart failure, eye disease. Most major diabetic societies suggest targeting blood pressures less than 130 systolic and less than 80 diastolic to improve outcome.

Treatment of high cholesterol in diabetes

Cholesterol abnormalities are common in diabetes. The most common findings are an increase in the triglycerides and a lowering of the HDL (good cholesterol). The LDL (bad cholesterol) is usually not significantly elevated but the type of LDL particles that are found in the diabetic patient may be more likely to result in heart and vascular disease. There is a substantial body of evidence that using statin drugs in diabetes improves outcome. There is some debate among the cardiac and diabetic societies as to when to treat, how aggressively to treat and what the goals of treatment should be. In general diabetics between the ages of 40-75 with risk factors for vascular disease or established vascular disease should be on statin therapy. The American College of Cardiology and the American Diabetes Association propose that all diabetes between the ages of 40-75 should be treated regardless of baseline cholesterol.

In our next article we will look at the impact of diabetic medications on the cardiovascular outcome of the diabetic patient.

Dr Ernest Madu, MD, FACC and Dr Paul Edwards, MD, FACC are consultant cardiologists for the Heart Institute of the Caribbean (HIC) and HIC Heart Hospital. HIC is the regional centre of excellence for cardiovascular care in the English-speaking Caribbean and has pioneered a transformation in the way cardiovascular care is delivered in the region. HIC Heart Hospital is registered by the Ministry of Health and Wellness and is the only heart hospital in Jamaica. Send correspondence to info@caribbeanheart.com or call 876-906-2107.

1 year 9 months ago

Jamaica Observer

'Biggest health risk of the 21st century'

PRESIDENT of the Medical Association of Jamaica Dr Brian James has made an impassioned plea to health-care workers to do something about what he describes as the biggest health risk of the 21st century — climate change.

Speaking at the launch of MDLink Diagnostic Laboratory on Thursday, Dr James, while underscoring that laboratory services are a crucial aspect of medical decision-making, said this generation will have to do something about the impact of climate change on health as it does not bode well for vulnerable populations.

"Some of the health impacts of global warming include a one-degree rise in temperature which translates to 3.4 per cent increase in cardiovascular mortality, Dr James said. "Crime precipitates mental health concerns. At higher temperatures there is an increase in the risk of work-related injuries and illnesses among indoor and outdoor workers. Outdoor workers, women, children, athletes and the elderly are at increased risk of heat-related injury."

Further, Dr James said climate change presents an increased risk in vector capacity for the transmission of dengue and food-borne diseases like salmonella.

Moreover, he said the largest impact of climate change in the health industry is that large carbon footprint.

"This means it's an area with a significant opportunity to play a part in mitigating the effects of climate change and global warming," he said before giving suggestions for the greening of the diagnostic lab environment.

To make the lab environment green, Dr James suggested lab operators and health-care workers start the discussion and make climate change and global warming a part of the new culture of the health environment; reduce laboratory plastic waste by implementing recycling and reusing strategies to reduce carbon footprint; conserve water; reduce energy consumption; share resources; and use greener techniques.

He added that he was confident MDLink will become an active and committed partner in climate action.

1 year 9 months ago

Jamaica Observer

A new era for Alzheimer's treatment begins

A proven treatment to slow down the progression of Alzheimer's — a devastating disease that robs individuals of their personality, autonomy, and ultimately life — has long been out of reach.

But within the next year, Alzheimer's patients could conceivably have access to not just one such treatment, but two.

A proven treatment to slow down the progression of Alzheimer's — a devastating disease that robs individuals of their personality, autonomy, and ultimately life — has long been out of reach.

But within the next year, Alzheimer's patients could conceivably have access to not just one such treatment, but two.

This new era for Alzheimer's treatment began this week, when the Food and Drug Administration (FDA) granted full approval to a new Alzheimer's drug, lecanemab, which is being sold by its manufacturer Eisai under the brand name Leqembi. Memory clinics are already reporting increasing curiosity among patients about the new treatment, and they expect interest will only grow following the FDA's final sign-off.

In the next few weeks, new clinical trial results are also expected for another treatment candidate, donanemab, which has had impressive preliminary results.

Just two years ago, the Alzheimer's community was in turmoil. An earlier drug, called aducanemab and known by the brand name Aduhelm, had reported disappointing clinical trial results, but the FDA, over the objections of its scientific advisers, still decided to grant "accelerated approval" to the drug, which has a lower threshold for approval and is reserved for drugs that address an unmet need. The controversy cast a pall over the medication, Medicare severely limited coverage, and few prescriptions were written for a treatment once hoped to be a breakthrough.

People who work in the field describe a community at war with itself, as some advocacy groups pushed for more access to aducanemab even as many clinicians remained unconvinced.

Lecanemab could offer a fresh start. The clinical data appears more promising. The FDA's advisers endorsed it last month. The preliminary results from donanemab appear even more impressive, though they need to be confirmed in forthcoming reports.

It is still a fraught moment for providers and patients. The treatments require an extensive patient evaluation before being prescribed, regular infusions in their administration, and careful monitoring over time to catch potentially dangerous side effects — all a challenge for the US health system. Not enough doctors are trained in caring for patients with memory problems. There are not enough infusion centres. Medicare covers some of the scans that could be used to identify patients who may benefit from lecanemab, but not others.

The logistical challenges could be daunting, said Sanjeev Vaishnavi, a clinical neurologist at the Penn Memory Center who is helping to lead its planning efforts. The centre sometimes has a months-long waiting list from patients who are seeking more specialised care than their primary care doctor is able to provide. If the demand for lecanemab is high, new patients could end up waiting for years — at which point, they may no longer benefit from the drug.

"I think the concern is, how can we deliver appropriate care to the right individuals in a timely manner?" Vaishnavi said, articulating his fear that patients could end up "stuck in a morass of bureaucracy".

Nevertheless, he said, "it's an exciting time."

Alzheimer's afflicts at least six million Americans. While only a subset may benefit from lecanemab, it holds enormous promise for those patients and their families — and for the many Alzheimer's patients who will follow in the years to come, as the country's population ages. This disease is distinct not only for its prevalence but also for the way it works. Over time, it wears away a person's personality and sense of self. Ultimately, it is 100 per cent fatal.

Science has searched for an effective treatment; for decades, potential breakthroughs would show promise and then flame out. The failures led some researchers in recent years to question the entire premise of most Alzheimer's research, though lecanemab may prove to be a kind of validation of the amyloid hypothesis that has driven drug development.

Jason Karlawish, the co-director at the Penn Memory Center, described his colleagues, patients, and their families as "travellers who finally see they arrived at land after traversing a dangerous ocean."

"I'd much rather be in this place than where things were two or three years ago," he told me. "This is what we've been waiting for for decades."

This story first appeared on
Vox
.
com.
It was written by Dylan Scott who has covered health care for
Vox
. He has reported on health policy for more than 10 years, writing for
Governing
magazine, Talking Points Memo and STAT before joining
Vox
in 2017. Read more:

https://www.vox.com/policy/2023/7/7/23784663/alzheimers-drug-lecanemab-leqembi-full-fda-approval

1 year 9 months ago

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