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Vaistų   reguliavimo   tendencijos Vaistų   reguliavimo   tendencijos

Vaistų reguliavimo tendencijos - PowerPoint Presentation

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Uploaded On 2020-08-04

Vaistų reguliavimo tendencijos - PPT Presentation

pacientų akimis LR Seimas 20180 9 19 Akcentai 2 IDEALIAME PASAULYJE 3 NaUJA SENA diskusija apie priemokas 4 NaUJA SENA diskusija apie priemokas 5 Aktualijos Lietuvoje 2018 m ID: 797047

quality patients medical generics patients quality generics medical diskusija protection payment design improve response case record switching priemokas apie

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Presentation Transcript

Slide1

Vaistų

reguliavimo

tendencijos pacientų akimisLR Seimas 2018-09-19

Slide2

Akcentai2

Slide3

IDEALIAME PASAULYJE3

Slide4

NaUJA / SENA diskusija apie priemokas

4

Slide5

NaUJA / SENA diskusija apie priemokas

5

Slide6

Aktualijos Lietuvoje 2018 m.6

Slide7

Rezonansiniai atvejai

7

Slide8

PACIENTAMS KYLANTYS klausimai8

Slide9

Priemokos nereceptinIAMs vaistams9

Slide10

Receptinių VS nERECEPTINIŲ VAISTŲ VARTOJIMAS

10

Slide11

Percentage co-payments + limited protectionVHI covering co-paymentsCaps on co-paymentsPoor people exemptFlat co-paymentsSource: WHO Barcelona Office 2018Financial protection is closely linked to co-payment design (medicines)

Improve co-payment design

Stronger financial protection

Slide12

Case Example from Blood Cancer Field(TKI generics):Patients welcome that generics may improve patient access to more affordable therapies in many countries. However, we also raise concerns about impact on the treatment outcomes when switched between different products for non-medical reasons, if equivalence of these products’ is still uncertain in terms of quality and efficacySee statement of the CML Advocates Network as of 21 May 2014:http://www.cmladvocates.net/133-generics/35412Patients ask for:reliable proof of quality and equivalence of pharmacokinetics and bioavailabilitycollection of comparative clinical data to ensure comparable efficacyno switching for non-medical reasons in optimal response and toleranceno switching between products of same compound more frequently than once a year to allow consistent follow-up, and in case of loss of response or increased toxicity, switch back or switch treatmentmore frequent monitoring (must: PCR tests, optional: plasma level

testing)

Slide13

Recommendations that Do not Cost: by Patients to Patients Record the date when started taking biosimilarTrack and record any changes of quality of life on biosimilarReport any noticeable adverse events to your treating physicianTell your physician that you have been switched to biosimilarBe willing to share your experience with patients communityEvery time you are renewing your prescription ask for the same biosimilar from the same manufacturer. Be ready to show the label / picture of the packaging to the pharmacist13

Slide14

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