Denis Kibira/Patrick Mubangizi HEPS Uganda/HAI- Afica Access to Medicines
Jun 14, 2015
Denis Kibira/Patrick MubangiziHEPS Uganda/HAI-Afica
Access to Medicines
Objectives of presentation
To understand What is meant by Essential Medicines Components of access to Essential Medicines RUM Drug donations and promotions Generic Vs Branded
Apr-09MeTA CSO Workshop2
Definitions
Essential Medicines
Are medicines that satisfy the needs of the majority of the population and therefore should be available all the time. World Health Organisation
A selection of these medicines according to the needs and disease burden of the country makes the Essential Medicines List
Apr-093
Access to essential drugsWHO framework for action
Apr-094
1. Rationalselection
4. Reliablehealth and
supply systems
2. Affordableprices
3. Sustainablefinancing
ACCESS
Essential medicines are intended to be available within the contest of functioning healthcare systems at all times, in adequate amounts, in appropriate dosage forms, with assured quality, and at a price the individual and community can afford.
Access
Apr-095
Available
Accessibility
Acceptability
Affordability
Access
Apr-096
4 As
Available – On shelves for dispensing to patients
Accessible – geographical or physical location of medicines
Acceptable – answering need, quality, generic/brand
Affordable by the target group
Apr-097
Rational Use of Medicines (RUM)
Right medicine, Right time, Right dose, Right cost, Right information
Appropriate indication Appropriate medicine – safe, efficacious, effective
(quality) Appropriate administration, dosage, duration Appropriate patient Appropriate patient information Appropriate evaluation
Apr-098
Drug donation
Core Principles: Maximum benefit to the recipient Respect for the wishes and authority of the
recipient No double standards in quality Effective communication between donor and
recepient
Drug Promotion
This is the advertising of medicines through the media (radio, TV, print); use of medical representatives, symposia
It should be ethical, with useful and unbiased information
Should conform to WHO criteria: reliable, accurate, truthful, informative, balanced, up to date, capable to substantiation, in good taste
Generic Vs Branded
Branded medicine: this is an innovator/originator medicine
Generic medicine: this is a copy of originator medicine containing exact active ingredients
Generics are substantially cheaper than brands as there are no costs related to R&D
Counterfeits/Substandard medicines
a medicine which is deliberately and fraudulently mislabelled with respect to identity and / or source
counterfeiting can apply to both branded and generic products and counterfeit products
may include products with the correct ingredients or with the wrong ingredients, without active ingredients, with insufficient active ingredients, or with fake packagingwww.who.int/medicines
over- or under- concentration of ingredients contamination poor quality ingredients poor stability inadequate packaging
Why are there substandard medicines? low standards of manufacturing (e.g. for export) weak regulatory agencies
What are substandard medicines?
Thank you!
Questions, comments …????
Apr-09MeTA Uganda 14