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Showing posts with label PHARM.D. Show all posts
Showing posts with label PHARM.D. Show all posts

Saturday, June 4, 2016

Elsevier Student Ambassador - 2016 : Apply Today

Dear Readers..!!! Thanks for visiting my blog...!!!

Elsevier is the world's leading information resource provider. Elsevier Student Ambassador (ESA) programme is one of the most thriving programmes of Elsevier South Asia giving you the chance to become a liaison between Elsevier and your college/University. The mandate of this programme is to have student ambassadors from health sciences community across South Asia who can connect with each other and open gates to unexplored opportunities in their fields.

Joining this programme empowers you to connect with your fellow ESA's across the South Asia, get access to the latest from Elsevier Information repository, and be a part of the team that will help in redefining the health care education in South Asia.


As a student ambassador, you will get many opportunities to upgrade your skills, connect with your peers and be the face of Elsevier. You would get an exclusive chance to become expert reviewers of Elsevier and also an opportunity to author with it. You would get to attend significant CMEs, author events, product launch events, conferences, group discussions etc., apart from having free trials of the rich Elsevier products once you are chosen as the ESA. And much more..

How to apply : "Become an ESA"

1) Register by entering your details

2) Login with your email id

3) Read the terms and conditions

4) Be a part of the medical quiz competition and answer 30 questions in 15 minutes and submit

5) Submit an Essay regarding the topic mentioned

6) Wait for the telephonic Interview

New Opportunities this year:
  1. Great Opportunity to Upgrade your skills through various Elsevier portals.
  2. Great opportunity to Author with Elsevier.
  3. Exclusive chance to become an expert Elsevier reviewer.
  4. Attend events, Product launch and Conferences. 


For those who want to skip Quiz; you need to get a referral from the already existing Ambassadors or Mentors.


Every year 10,000 students apply for this programme from various counties of which only 100 will be selected and get benefited, hope you will be one among them this year. All the best. 


Official Website: "Elsevier India"


Happy Blogging...!!!

Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Sunday, May 29, 2016

How to Become a Registered Pharmacist in India

Dear Readers..!!! Thanks for visiting my blog...!!!



Application Procedure : 

The candidate has to be Registered at your respective State Pharmacy Councils through this procedure


Happy Blogging...!!!

Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India

Elsevier Student Ambassador - South Asia

    Wednesday, May 25, 2016

    Good News for Pharm.D graduates : Tata Memorial Centre Fellowships

    Dear Readers..!!! Thanks for visiting my blog...!!!



    Apply Here

    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    Sunday, May 22, 2016

    New Study Reveals Tamoxifen Reduces Breast Cancer Rates by Nearly a Third for 20 Years

    Dear Readers..!!! Thanks for visiting my blog...!!!

    A new study has shown that the preventive effect of the breast cancer drug, tamoxifen, remains virtually constant for at least 20 years, with breast cancer rates reduced by around 30 percent. Median 16-year follow-up results from the IBIS-I (International Breast Cancer Intervention-I) trial show a 29% lower risk for developing breast cancer among women who had been randomly assigned to five years of tamoxifen than for women assigned to five years of placebo.


    “Tamoxifen is a well-established and effective treatment for certain breast cancers, but we now have evidence of its very long-term preventive benefits…" said Professor Jack Cuzick, IBIS-I lead author and Head of the Centre for Cancer Prevention at Queen Mary University of London. Professor Cuzick underscored the “strong and unabated” 20-year preventive effect of breast cancer resulting in a reduction in breast cancer rates of around a third. “We hope these results will stimulate more women, particularly younger women, to consider treatment options for breast cancer prevention if they have a family history of the disease or other major risk factors.”

    The IBIS-I results were presented on December 11, 2014 at the San Antonio Breast Cancer Symposium (SABCS 2014) in Texas and published simultaneously in The Lancet Oncology. SABCS is an international scientific symposium for interaction and exchange among basic scientists and clinicians in breast cancer.

    It was organized by the Cancer Therapy & Research Center at UT Health Science Center San Antonio, the American Association for Cancer Research, and Baylor College of Medicine. The IBIS-I study, which began recruitment in 1992, enrolled 7,154 pre- and post-menopausal women aged from 35 to 70 years at high risk for breast cancer primarily because of a family history. They were randomly assigned to receive either tamoxifen 20 mg daily for five years (3,579) or placebo (3,575).

    Hormone replacement therapy was allowed during the trial and was used by 49.5% in the placebo group, and approximately 35% of women in each group had had a hysterectomy. The median age at enrollment was 50.8 years in each group. At a median of 16 years of follow-up (longest follow-up 22 years), there were 601 breast cancers reported, 251 (7.0%) occurring in women who took tamoxifen, and 351 (9.8%) in women who took placebo.

    In subanalysis, the most pronounced reductions in risk were seen for invasive estrogen-receptor-positive (ER+) breast cancer and ductal carcinoma in situ. However, tamoxifen did not significantly reduce the risk for invasive estrogen-receptor-negative (ER-) breast cancer. The extended analysis of the IBIS-I trial was announced a year after the first results of the IBIS-II trial were released, which found taking the breast cancer drug anastrozole (an aromatase inhibitor) for five years reduced the chances of post-menopausal, high-risk women developing the disease by 53% compared with women who took a placebo. Professor Cuzick concludes: “For most post-menopausal women, an aromatase inhibitor such as anastrozole should be the drug of choice, as it is more effective than tamoxifen and has fewer side effects. However… “…for most premenopausal, high-risk women, tamoxifen remains the only drug of choice for breast cancer prevention and it is a good one, as shown by this new evidence.”

    Most Filipino patients cannot afford cost of breast cancer screening, treatment

    In the Philippines, which has the highest rate of breast cancer in Asia, low awareness may not be the main reason why the majority of breast cancer cases are not diagnosed early. “Most Filipino patients cannot afford the cost of diagnostic tests and treatments for breast cancer,” states the 2010 Philippine Cancer Facts and Estimates, a document published by the Department of Health and Philippine Cancer Society.

    Experts recommend that women, starting at the age of 30, perform monthly self breast examination (SBE) and undergo an annual clinical breast examination (CBE) performed by a healthcare professional. Annual mammogram is recommended for women beginning age 40. According to the 2010 Philippine Cancer Facts and Estimates, national breast cancer awareness campaigns which do not include the provision of diagnosis and treatment are outdated and ineffective. It recommended that each province, city, municipality and barangay should establish and implement its own program for breast cancer diagnosis and treatment.

    For such a program to succeed and be sustainable, local government officials, insurance providers, NGOs and civic-minded individuals and organizations, health workers and medical specialty societies must work together in providing access to breast cancer screening and treatment.

    References:





    4. http://www.philhealth.gov.ph/news/2012/z_benefits.html

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    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    Friday, May 20, 2016

    Mercy killing - A new lease of life : Palliative Medicine

    Dear Readers..!!! Thanks for visiting my blog...!!!

    Our Sincere Thanks to Dr. Gayatri Palat, MD for sharing with us.  


    Addressing the contentious issue of mercy killing, the government has come up with a draft Bill on passive euthanasia which will give a patient the right to withhold from medical treatment in case they are terminally ill.


    The Union Health Ministry has drafted and put up ‘The Medical Treatment of Terminally Ill Patients (Protection of Patients and Medical Practitioners) Bill’ in the public domain for consultation with stakeholders.


    The Bill intends to provide protection to patients and medical practitioners from liability in the context of withholding or withdrawing medical treatment, including life support systems, from those who are terminally ill. According to the Bill, every “competent” person, including minors aged over 16, has a right to decide on withholding or withdrawing medical treatment and to allow nature to take its own course or for starting medical treatment in case of terminal illness.

    The Bill goes on to say that such a decision will be binding on the medical practitioner. He or she has to inform the spouse, parents or any other close relative of the patient and desist from carrying out the decision for a period of three days after informing them.

    However, despite withdrawing the medical treatment, the said doctor can keep administering palliative care to the patient. The draft Bill gives legal cover to both patients and medical practitioners.

    The Medical Council of India has been given the authority to formulate guidelines from time to time for the guidance of medical practitioners and might review and modify the guidelines periodically.

    In case any patient is not competent enough to take a decision then his or her next of kin, including spouse, parents or sibling, can approach the High Court, which will have to take a decision within a period of one month.

    The government first attempted to formulate a law in 2006, based on a report of the Law Commission. However, the ministry had at that time decided not to take any action. The Supreme Court had laid down comprehensive guidelines in the Aruna Shanbaug case to process passive euthanasia. Active euthanasia is different from the passive form and involves injecting the patient with a lethal substance causing death in a painless manner.

    The Aruna Shanbaug story

    The debate on euthanasia caught the public attention in Aruna Shanbaug’s case. Aruna died in 2015 after being in a Permanent Vegetative State for over 40 years. While rejecting the plea for her mercy killing, SC laid out the first set of guidelines for euthanasia

    What happened to Aruna?

    Aruna, a nurse at King Edward Memorial Hospital in Mumbai, was sexually assaulted by a sweeper in 1973. He choked her with a dog chain causing severe brain damage. She was discovered only the next day.



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    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    Friday, March 25, 2016

    Indian Pharmacovigilance : What is known is just Half -Glass Full

    Dear Readers..!!! Thanks for visiting my blog...!!!

    Background

    Spontaneous or voluntary reporting of suspected adverse drug reactions (ADRs) is one of the vital roles of all health professionals. In India, under-reporting of ADRs by health professionals is recognized as one of the leading causes of poor ADR signal detection. Therefore, reviewing the literature can provide a better understanding of the status of knowledge, attitude and practice (KAP) of Pharmacovigilance (PV) activities by health professionals.



    Methods

    A systematic review was performed through Pubmed, Scopus, Embase and Google Scholar scientific databases. Studies pertaining to KAP of PV and ADR reporting by Indian health professionals between January 2011 and July 2015 were included in a meta-analysis.

    Results

    A total of 28 studies were included in the systematic review and 18 of them were selected for meta-analysis. Overall, 55.6% (95% CI 44.4–66.9; p<0.001) of the population studied were not aware of the existence of the Pharmacovigilance Programme in India (PvPI), and 31.9% (95% CI 16.3–47.4; p<0.001) thought that "all drugs available in the market are safe". Furthermore, 28.7% (95% CI 16.4–40.9; p<0.001) of them were not interested in reporting ADRs and 74.5%, (95% CI 67.9–81.9; p<0.001) never reported any ADR to PV centers.

    Conclusion

    There was an enormous gap of KAP towards PV and ADR reporting, particularly PV practice in India. There is therefore an urgent need for educational awareness, simplification of the ADR reporting process, and implementation of imperative measures to practice PV among healthcare professionals. In order to understand the PV status, PvPI should procedurally assess the KAP of health professionals PV activities in India.



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    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    Thursday, March 10, 2016

    Drugs acting on Cardiovascular System : Classification at tips

    Dear Readers..!!! Thanks for visiting my blog...!!!









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    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India

    Elsevier Student Ambassador - South Asia

    Vacancies for PharmD and M.Pharm freshers

    Dear Readers..!!! Thanks for visiting my blog...!!!


    For more Updates, follow us on Facebook

    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    Friday, February 26, 2016

    Vacancies in Indian Pharmacopoeia Commission (IPC) : Pharm.D Freshers

    Dear Readers..!!! Thanks for visiting my blog...!!!

    The Indian Pharmacopoeia Commission (IPC) is an Autonomous Body under Ministry of Health & Family Welfare, Govt. of India primarily with the objectives of regularly updating the Indian Pharmacopoeia by publishing new edition and its addenda, National Formulary of India and other related tasks such as preparing, certification and distribution of reference substances & functions as National Coordination Centre (NCC) for Pharmacovigilance Programme of India (PvPI). We are looking forward for qualified personnel to fill up 40 posts of Technical Associates (for NCC & ADR Monitoring Centres) in PvPI on Contract basis having Master’s Degree in Pharmaceutical Sciences or M.B.B.S/ B.D.S/ Pharm. D or equivalent. Preference will be given to young, dynamic personnel having experience in Pharmacovigilance and proficiency in Computer Applications. Consolidated emolument @ Rs. 25,000/- per month will be paid by IPC. 

    The job description of the post is:- 
    • Collection of ADR Reports.
    • Follow up with the reporter/patient for Completeness as per SOPs. Data Entry in VigiFlow.
    • Reporting to NCC-PvPI through VigiFlow with the source data (Original) attached each ADR case.
    • Training/Sensitization/Feedback to physicians through news letter circulated by the NCCPvPI.
    Other activities as assigned by competent authority from time to time. Applications are invited from citizens of India on the application format which can be downloaded from the website: www.ipc.gov.in of the Commission together with the attested copies of supporting documents within 15 days from the date of advertisement. The competent authority reserves the right to increase or decrease the number of vacancies and rejection and/or all applications received without assigning any reason. Selected candidates shall be posted in any of the AMCs under PvPI across the country/NCC-PvPI, IPC, Ghaziabad.


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    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    Monday, February 22, 2016

    How to Become a Registered Pharmacist in U.K

    Dear Readers..!!! Thanks for visiting my blog...!!!

    General Pharmaceutical Council (GPhC) governing the pharmacist registration in UK, and as an Overseas pharmacist we have to fulfill these requirements.


    Step 1: An Overseas Pharmacists Assessment Programme (OSPAP)
    Step 2: 52 weeks of Pre-registration training approved by the GPhC 
    Step 3: The registration assessment Examination.

    Step 1: Overseas Pharmacists' Assessment Programme (OSPAP):



    OSPAP is a one-year post graduate diploma course designed to ensure that those who have qualified overseas receive the appropriate education and training to prepare them for UK Practice and entry to Pre-registration training. Entry to these course needs English language proficiency of IELTS testing at level 7 in each category at a single test.

    • Aston University (Birmingham) 
    • University of Brighton
    • Kingston University
    • Robert Gordon University (Aberdeen)
    • University of Sunderland
    Step 2: 52 weeks of Pre-registration training approved by the GPhC:

    On graduation you will be eligible to apply for preregistration training for a one-year period prior to taking up the registration examination of the General Pharmaceutical Council (GPhC).

    Step 3: The registration assessment Exam:

    There are two examination papers; an open-book and a closed book paper. Questions are based on practice-based situations and are designed to test the thinking and knowledge which lie behind any action.

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    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    Sunday, February 21, 2016

    How to Become a Registered Pharmacist in Australia

    Dear Readers..!!! Thanks for visiting my blog...!!!


    Australian Pharmacy Council (APC) governing the pharmacy Exam in Australia.



    Step 1: Document Evaluation.
    Step 2: English Competency Examination.
    Step 3: KAPS (Knowledge Assessment of Pharmaceutical Exam)
    Step 4: Pharmacy Board of Australia (PBA) requirements for registration.

    Step 1: Document Evaluation:

    An initial assessment of a candidate’s qualifications and associated documents is undertaken to determine an applicant's eligibility to undertake the secondary assessment which is the knowledge assessment (KAPS) for Stream A or the competency assessment (CAOP) for Stream B.

    Step 2: English Competency Examination:

    An overall Band score of at least 7.5(with a minimum score of 7.0 in each of the four components) at the Academic level of IELTS is an essential prerequisite for enrollment in the KAPS (as used in Stream A).

    Step 3: Knowledge Assessment of Pharmaceutical Sciences (KAPS)

    The KAPS consists of two papers of multiple choice questions covering pharmaceutical chemistry, pharmaceutics, pharmacology and physiology, and therapeutics. It is held in Australia and overseas in March and September each year.

    Step 4: Pharmacy Board of Australia (PBA) registration requirements

    1-Supervised practice in an Australian pharmacy under the direct supervision of a registered pharmacist (1824 hours)

    2-An intern training program.
    -attendance at seminars and workshops
    -completion of assessment tasks

    3-A written examination.

    4-A oral examination.


    Examination
    Expense per Exam


    Total
    2820 AUD
    Document Evaluation + IELTS
    500 + 200 AUD
    Stream A – Secondary Assessment – KAPS
    1600 AUD
    PBA Written Examination prepared and   delivered by APC
    550 AUD

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    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    How to Become a Registered Pharmacist in USA

    Dear Readers..!!! Thanks for visiting my blog...!!!


    National Association Board of Pharmacy (NABP) is conducting pharmacy Exam in USA. Refer: http://www.nabp.net/


    There are 3 steps to achieve NABP pharmacist certification for International students.

    Step 1: Document Evaluation by ECE
    Step 2: The Pharmacist Equivalence examination certification by FPGEC
    Step 3: The NAPLEX Examination

    Step 1: Document Evaluation by ECE:

    Evaluation Credential evaluation (ECE) is a separate non profit organization, evaluating you educational document equivalence with USA degree. Refer: http://www.ece.org/

    We easily qualify that by sending our PharmD degree and transcript according to their requirements.

    Step 2: The Pharmacist Equivalence examination certification by FPGEC:

    FPGEC is Foreign Pharmacist Graduate Equivalence Examination Certificate required by International students by fulfilling two requirements.

    1-FPGEE (Foreign Pharmacist Graduate Equivalence Exam) :

    2-TOEFL iBT (Computerized Based) requirement :
    Reading: 21
    Listening: 18
    Speaking: 26
    Writing: 24. 

    Step 3: The NAPLEX Examination :

    You must get FPGEC to qualify for the NAPLEX exam. NAPLEX is a nationwide exam used by boards of pharmacy as one component of pharmacist licensure.

    Examination
    Expense per Exam


    Total
    1365 USD

    Step 1 : ECE Evaluation
    80 USD
    Step 2 : FPGEE+ TOEFL iBT
    800 + 200 USD
    Step 3: NAPLEX
    485 USD

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    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

    How to Become a Registered Pharmacist in Canada

    Dear Readers..!!! Thanks for visiting my blog...!!!

    Pharmacy Examination are conducted under the control of PEBC 

    (Pharmacy Examination Board of Canada) : http://www.pebc.ca



    There are 3 steps for an International student to achieve PEBC pharmacist certification:

    Step 1: Document Evaluation.
    Step 2: The Pharmacist Evaluating Examination.
    Step 3: The Pharmacist Qualifying Examination, Part I (MCQ) and Part II (OSCE).

    Step 1: Document Evaluation:

    You must pass this evaluation of your educational and professional credentials to be eligible to write the Pharmacist Evaluating Examination (We easily qualify that).

    You must pass this written examination to be eligible for the Pharmacist Qualifying Examination –Parts I and II (You have to go through all pharmacy course once to pass this exam).

    Step 2: The Pharmacist Evaluating Examination:

    You must pass this written examination to be eligible for the Pharmacist Qualifying Examination –Parts I and II (You have to go through all pharmacy course once to pass this exam).

    Step 3: The Pharmacist Qualifying Examination, Part I (MCQ) (Written) and Part II (OSCE) (Verbal).

    Your final step to qualifying for certification with PEBC. When you have passed both Parts of the examination you will be certified and registered with PEBC as Qualified Pharmacist.

    For this portion you have to really work hard and proper understanding of Drug and therapeutics.

    Need 1000 hour of internship and IELTS 6.5 to get register with PEBC. Then after that job is not a issue, Drug store will be chasing you for Job.

    Examination
    Expense per Exam
    Step 1 : Document Evaluation
    530 CAD
    Step 2 : Pharmacist Evaluation Exam
    515 CAD
    Step3 : MCQs and OSCE
    400+1520 CAD

    Total
    2965 CAD

    For more Updates, follow us on Facebook

    Happy Blogging...!!!

    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia