EVENT

Main information

  • Trade name:
  • EVENT 10 TAB
  • Pharmaceutical form:
  • TAB
  • Composition:
  • 10
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • EVENT 10 TAB
    India
  • Language:
  • English

Other information

Status

  • Source:
  • Central Drugs Standard Control Organization
  • Last update:
  • 09-08-2016

18-4-2018

The impact of global change on the emergence of plant diseases and pests in Europe

The impact of global change on the emergence of plant diseases and pests in Europe

The French Agency for Food, Environmental and Occupational Health and Safety (ANSES), in collaboration with the European Food Safety Authority (EFSA) and the European and Mediterranean Plant Protection Organization (EPPO), is organising a conference on 23-24 April 2018 in Paris. This two-day event will review the current state of scientific knowledge worldwide and provide a forum for sharing experiences on the reasons for the emergence of plant diseases and pests, as well as their impact on the environme...

France - Agence Nationale du Médicament Vétérinaire

4-4-2018

FDA Adverse Event Reporting System (FAERS): Latest Quarterly Data Files

FDA Adverse Event Reporting System (FAERS): Latest Quarterly Data Files

FDA Adverse Event Reporting System (FAERS) - Quarterly Data Extract (QDE): The Quarterly Data Extract files, contain raw data extracted from the FAERS database for the indicated time ranges (not cumulative), in ASCII or SGML formats.

FDA - U.S. Food and Drug Administration

15-3-2018

Louis Garneau Sports Inc. recalls Course LG1261 Cycling Helmets

Louis Garneau Sports Inc. recalls Course LG1261 Cycling Helmets

The plastic shell on the helmet can weaken over time causing the product to fail head impact testing. In the event of an accident, the helmet could fail to prevent head injuries, posing a hazard to consumers.

Health Canada

13-2-2018

ANSES at the 2018 Paris International Agricultural Show: collective expert appraisal devoted to health

ANSES at the 2018 Paris International Agricultural Show: collective expert appraisal devoted to health

Like every year, ANSES will be at the Paris International Agricultural Show (SIA), a key annual event providing the opportunity to meet with its partners and the general public. As an agency responsible for health risk assessment, ANSES participates fully in this event, to promote its work devoted to health and safety. The Agency invites visitors to find out more about its activities in food safety, animal health and welfare, and plant health. Language English

France - Agence Nationale du Médicament Vétérinaire

1-2-2018

Hongkong Sun Rise Trading Limited recalls Kobalt and Greenworks Cordless Electric Chainsaws

Hongkong Sun Rise Trading Limited recalls Kobalt and Greenworks Cordless Electric Chainsaws

In the event of chainsaw kickback, an affected chain brake guard could fail to activate the micro switch intended to stop the motor, which could allow the chain to continue moving. This can pose a risk of a laceration to the user or a bystander.

Health Canada

13-12-2017

Risks of ingestion of button batteries by young children: adopt the right reflexes in the event of an accident

Risks of ingestion of button batteries by young children: adopt the right reflexes in the event of an accident

(Soon in English) Language English

France - Agence Nationale du Médicament Vétérinaire

11-10-2017

Statement by FDA Commissioner Scott Gottlieb, M.D. on new steps by FDA to advance patient engagement in the agency’s regulatory work

Statement by FDA Commissioner Scott Gottlieb, M.D. on new steps by FDA to advance patient engagement in the agency’s regulatory work

The Food and Drug Administration is hosting a pioneering event today: the first meeting of the Patient Engagement Advisory Committee or PEAC. It’s a significant step forward in the FDA’s efforts to broaden its engagement with patients – and to deepen the involvement of patients in our regulatory activities.

FDA - U.S. Food and Drug Administration

11-10-2017

Parts Canada recalls Icon Motorcycle Helmets

Parts Canada recalls Icon Motorcycle Helmets

Due to a sewing problem in the chin strap, the faulty stitching may allow the D-rings to separate from the chin strap. In the event of a crash, the wearer of the helmet may not be adequately protected, increasing the risk of personal injury or death.

Health Canada

4-10-2017

ANSES celebrates science

ANSES celebrates science

The annual Fête de la Science (Science Festival) is the ideal event for promoting scientific research and its various professions. As a health agency with eleven research and reference laboratories, ANSES participates fully in this festival, giving the public a special insight into the work of its scientists and their passion for science devoted to health and safety. Various events will thus be on offer all over France from 6 to 15 October 2017, enabling the population to discover or rediscover ANSES's e...

France - Agence Nationale du Médicament Vétérinaire

2-10-2017

Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s Adverse Event Reporting System (FAERS) and new search tool

Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s Adverse Event Reporting System (FAERS) and new search tool

Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s Adverse Event Reporting System (FAERS) and new search tool

FDA - U.S. Food and Drug Administration

28-9-2017

FDA improves access to reports of adverse drug reactions

FDA improves access to reports of adverse drug reactions

The U.S. Food and Drug Administration today launched a new user-friendly search tool that improves access to data on adverse events associated with drug and biologic products through the FDA’s Adverse Event Reporting System (FAERS). The tool is designed to make it easier for consumers, providers, and researchers to access this information.

FDA - U.S. Food and Drug Administration

25-9-2017

TAH-t Companion 2 Driver System (C2) and Freedom Driver System by SynCardia Systems:  Letter to Health Care Providers - Mortality and Neurological Adverse Event Results

TAH-t Companion 2 Driver System (C2) and Freedom Driver System by SynCardia Systems: Letter to Health Care Providers - Mortality and Neurological Adverse Event Results

UPDATED 09/25/2017. Most recent interim results from the ongoing SynCardia TAH-t post-approval study looking at mortality and neurological adverse events.

FDA - U.S. Food and Drug Administration

11-9-2017

Hurricane Season: Be Prepared

Hurricane Season: Be Prepared

It's important to safeguard your food, water, and medicine before, during and after any severe weather event.

FDA - U.S. Food and Drug Administration

3-7-2017

Adverse event reports for centrally authorised veterinary medicinal products should not be sent to the DKMA

Adverse event reports for centrally authorised veterinary medicinal products should not be sent to the DKMA

The Danish Medicines Agency no longer requests the direct transfer of serious and unexpected third-country adverse event reports for centrally authorised veterinary medicinal products.

Danish Medicines Agency

3-7-2017

 Adverse event reports for centrally authorised veterinary medicinal products should not be sent to the DKMA

Adverse event reports for centrally authorised veterinary medicinal products should not be sent to the DKMA

The Danish Medicines Agency no longer requests the direct transfer of serious and unexpected third-country adverse event reports for centrally authorised veterinary medicinal products. Consequently, the reports should only be sent to EVVET (EudraVigilance Veterinary – the European, veterinary adverse event database administered by the EMA).

Danish Medicines Agency

6-4-2018

It’s #NationalPublicHealthWeek and the FDA wants you to be informed on how to report adverse events when using medical devices. Check out the FDA’s Safety Information and Adverse Event Reporting Program  https://go.usa.gov/xQ4Kd 

It’s #NationalPublicHealthWeek and the FDA wants you to be informed on how to report adverse events when using medical devices. Check out the FDA’s Safety Information and Adverse Event Reporting Program https://go.usa.gov/xQ4Kd 

It’s #NationalPublicHealthWeek and the FDA wants you to be informed on how to report adverse events when using medical devices. Check out the FDA’s Safety Information and Adverse Event Reporting Program https://go.usa.gov/xQ4Kd 

FDA - U.S. Food and Drug Administration

5-4-2018

Adverse events (‘side effects’) reporting survey

Adverse events (‘side effects’) reporting survey

Short survey to help us improve the way we collect and use adverse event reports to safeguard all Australians

Therapeutic Goods Administration - Australia

19-3-2018

News and press releases:  Workshop on Paediatric Regulation – stakeholders to discuss how to boost development of medicines for children

News and press releases: Workshop on Paediatric Regulation – stakeholders to discuss how to boost development of medicines for children

Event to be broadcast live on 20 March

Europe - EMA - European Medicines Agency

21-2-2018

Agenda:  Agenda - European Medicines Agency veterinary innovation day

Agenda: Agenda - European Medicines Agency veterinary innovation day

The objective of this meeting is to further raise awareness of the support available to facilitate innovation of veterinary medicines by giving an overview of the legislative framework and by describing the support offered by the European Medicines Agency (EMA ) and interactions with stakeholders. This event is open to all companies and stakeholders developing veterinary medicinal products.

Europe - EMA - European Medicines Agency

21-2-2018

Agenda:  Agenda - European Medicines Agency veterinary medicines innovation day

Agenda: Agenda - European Medicines Agency veterinary medicines innovation day

The objective of this meeting is to further raise awareness of the support available to facilitate innovation of veterinary medicines by giving an overview of the legislative framework and by describing the support offered by the European Medicines Agency (EMA ) and interactions with stakeholders. This event is open to all companies and stakeholders developing veterinary medicinal products.

Europe - EMA - European Medicines Agency

21-11-2017

MI Linked to Increased Vascular Dementia, Not Alzheimer's

MI Linked to Increased Vascular Dementia, Not Alzheimer's

A history of MI is associated with an increased risk of vascular dementia by as much as 35%, with the higher risk extending as far as 35 years after the event, results of a population-based study suggest[1].

US - RxList

31-10-2017

Scientific guideline:  Concept paper on the need for a paediatric addendum of the guideline on clinical investigation of medicinal products for the treatment and prophylaxis of venous thromboembolic disease, draft: consultation open

Scientific guideline: Concept paper on the need for a paediatric addendum of the guideline on clinical investigation of medicinal products for the treatment and prophylaxis of venous thromboembolic disease, draft: consultation open

A number of new European Medicines Agancy guidelines related to clinical investigation of medicinal products for the treatment and prophylaxis of venous thromboembolism (VTE) are already available [1,2,3], but recommendations are applicable only to adults. In contrast to adults, VTE in children is a rare event, but represents a significant management dilemma that requires therapeutic intervention. A paediatric addendum to the guidelines on clinical investigation of medicinal products for the treatment an...

Europe - EMA - European Medicines Agency

12-10-2017

Black Triangle Scheme

Black Triangle Scheme

Encouraging adverse event reporting helps us build the full picture regarding new medicines

Therapeutic Goods Administration - Australia

6-10-2017

Mammography Facility Adverse Event and Action Report: Jack County Hospital District dba Faith Community Hospital  https://go.usa.gov/xnchb 

Mammography Facility Adverse Event and Action Report: Jack County Hospital District dba Faith Community Hospital https://go.usa.gov/xnchb 

Mammography Facility Adverse Event and Action Report: Jack County Hospital District dba Faith Community Hospital https://go.usa.gov/xnchb 

FDA - U.S. Food and Drug Administration

5-10-2017

Mammography Facility Adverse Event & Action Report: Allen County Kansas Hospital dba Allen County Regional Hospital  https://go.usa.gov/xnc68 

Mammography Facility Adverse Event & Action Report: Allen County Kansas Hospital dba Allen County Regional Hospital https://go.usa.gov/xnc68 

Mammography Facility Adverse Event & Action Report: Allen County Kansas Hospital dba Allen County Regional Hospital https://go.usa.gov/xnc68 

FDA - U.S. Food and Drug Administration

22-8-2017

T3 To file an adverse event report with FDA go to  http://www.fda.gov/medwatch  #healthycontactschat

T3 To file an adverse event report with FDA go to http://www.fda.gov/medwatch  #healthycontactschat

T3 To file an adverse event report with FDA go to http://www.fda.gov/medwatch  #healthycontactschat

FDA - U.S. Food and Drug Administration