prescriptions and drug classes and exemptions Flashcards

(41 cards)

1
Q

what does the legal classes of medicines determine?

A
  • affect how patients can obtain them
  • who can order, give AND administer medicines
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2
Q

three legal classes

A

GSL = General sale list (e.g. in gas stations etc)

P = Pharmacy meds

POM = Prescription only medicine (only under authorised prescriptions)

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3
Q

what is pgd, under pom’s

A

under POMS →some are PGD = Patient group direction: can be given to patients without needing prescriptions e.g. flu vaccine

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4
Q

what are po meds

A

legally classified as a GSL med, but usually advice needed to be given with them, so can only be sold from a pharmacy

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5
Q

why are medicines classified in this way?

A

To enable access to medicines without having to see a doctor
Allow people to self-care and manage their conditions.
Limit overdose risk, limit access to medicines that could cause addiction
Ensures that medicines are supplied with appropriate advice
Safety – Some medicines are too unsafe to be on general sale (cytotoxic)

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6
Q

examples of POM-P Switch meds

A
  • Amorolfine Nail Laquer: fungal nail infections
  • Levonorgestrel and ulipristal: emergency contraceptives
  • Proton Pump Inhibitors (Omeprazole, pantoprazole): acid reflux
  • Sumatriptan: migraines
  • Tranexamic acid: heavy menstrual bleeding
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7
Q

how long are prescriptions valid for

A

6 months

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8
Q

what are prescriptions

A
  • document details medicine to be dispensed
  • individual named patient
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9
Q

prescriptions are written by who

A
  • written by authorised prescriber / practitioner
  • each medicine listed = prescription item
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10
Q

a prescription fulfils what 3 roles

A

clinical document, legal document, invoice

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11
Q

prescriptions come in what forms

A

electronic or paper

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12
Q

examples of prescribers

A

PRESCRIBERS
|
|– Doctors
|
|– Dentists
|
|– Vets
|
|– Non-medical prescribers
|
|– Pharmacists
|
|– Nurses
|
|– Opticians
|
|– Specialists with training

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13
Q

main 3 types of prescription

A

community, hospital and private

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14
Q

traits of NHS community prescriptions

A
  • only to be used for NHS patients
  • differ in colour and format by devolved nation
    FP10 - GPs = green prescription
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15
Q

traits of NHS hospital prescriptions

A
  • only to be used for NHS patients:
    -> Inpatient (STAY IN HOSPITAL) & outpatient (VISITING E.G FOR A CLINIC)
  • May include electronic prescribing systems → format varies
    -Drug chart (known as the prescription) also includes administrative record.
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16
Q

traits of private prescriptions

A

mostly same info as nhs scripts, just no set template
- no standard format except controlled drugs
- has qualifications of the prescriber e.g. doctors etc
- all vet prescriptions

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17
Q

NHS prescription journey - community

A
  • Patient visits GP
    • Prescription is issued as appropriate
    • Patient takes to community pharmacy or accessed electronic prescription
    • Prescription is clinically checked and medicines dispensed & accuracy checked, plus check details e.g. DOB, if they’re medically exempt
      • Patient counselled and takes medicines away
18
Q

what happens after the patient is counselled

A

Prescription goes to NHS Business Services Authority (NBSA) for pricing & payment

19
Q

prescription legal requirements: (7)

A
  1. signature of appropriate practitioner (indelible ink)
  2. Address of the appropriate practitioner
  3. Appropriate Date on which signed
  4. Particulars of the prescriber
  5. Patient NAME
  6. Patient Address
  7. Patient Age if under 12 years old
20
Q

do the same reqs apply to private and public prescriptions

21
Q

where are medical exemptions shown

A

(all shown on the back of the prescription AKA its receipt)

22
Q

examples of exemptions

A
  • low income
  • benefits
  • medical conditions like diabetes
  • maternity leave / after birth
  • armed forces
  • age e.g. under 18 & full time education
23
Q

medical abbreviations: time

A
  • x /7 indicates a number of days
  • x/52 indicates a number of weeks
  • x/12 indicates a number of months
24
Q

latin dosage abbreviations

A
  • 1 od – omni die – one each day
  • 1 om – omni mane – one each morning
  • 1 on – omni nocte – one at night
  • b.d or b.i.d – bis die / bis in die – twice a day
  • t.d.s – ter die sumendus – three times a day
  • q.d.s – quarter die sumendus – four times a day
25
What is a clinical check of a prescription?
“The purpose of a clinical check by a pharmacist is to ensure that the medicine supplied is both safe and effective for use by a particular patient in relation to the risk and benefit to the patient”
26
Aspects of a clinical check: what do we look out for?
- is the medicine right for the presenting patient - is the medicine right for the presenting condition - is the dosage appropriate - is the formulation appropriate - are there any interactions with the patients existing meds
27
THE 3 KEY ELEMENTS OF A CLINICAL CHECK
1. the patient 2. the medication 3. administration and monitoring of the prescribed medication
28
things we look at when considering administration of med
- route suitable - does the prescribed preparation exist - does it need to be taken with food - any adherence aids needed? - does any monitoring need to happen during treatment - any extra devices to get the best out of their medicine e.g. spacer for inhaler
29
Patient factors: the type of patient
- who are they? do they fall into a group where treatment is cautioned or contra-indicated - specific patients that fall into these groups = children, pregnant/breastfeeding, and elderly - consider gender, certain ethnic groups, and past or present drug use - consider intolerences / preferences: allergies, dietary intolerances & religious beliefs - if there are any co-morbidities (conditions to check as we may have to adjust doses etc)
30
cautioned meaning
when the drug should be used with care to avoid any danger or personal risk
31
contra-indicated meaning
when the drug should not be used because it may be harmful to the patient: can be relative & absolute
32
medication factors - what do we look at:
- whether the medication has any interactions with the patients other drugs, maybe even antagonistic ones - it’s indication of the medication, whether treatment is appropriate, if its within recommended guidelines - if the prescription or it’s strength or dose has changed
33
checking if the dose, freq & strength is appropriate includes looking at
- age - renal or hepatic function - weight - lifestyle patterns - co-morbidities - other drug treatments - whether it’s appropriate for the formulation
34
GSL medicines are medicinal products that can be sold or supplied to the public without a prescription or pharmacist supervision, provided they are what?
pre-packed and sold from premises that can be closed to exclude the public.
35
What are the legal storage requirements for GSL medicines?
Stable at ambient temperatures Stored in a clean, tidy environment Protected from direct sunlight and moisture Kept in their original packaging Have facilities that can be locked when premises are closed
36
What sales restrictions apply to GSL medicines?
GSL medicines: Must be pre-packed by the manufacturer Are subject to legal maximum pack size limits (e.g., 16 tablets for paracetamol in supermarkets) Cannot be sold if expired or damaged Must have patient information leaflets included Must be sold in child-resistant packaging where required by law
37
What are the legal requirements for P medicines?
Must be sold under the supervision of a registered pharmacist Must be sold from registered pharmacy premises Require the pharmacist to be available on the premises Cannot be self-selected by customers in most cases (must be requested)
38
How must P medicines be stored in a pharmacy?
Stored behind the pharmacy counter or in areas inaccessible to the public Kept in appropriate temperature-controlled environments (typically 2-25°C) Protected from unauthorized access Stored according to manufacturer specifications Subject to regular stock rotation and expiry date checks
39
What criteria determine if a medicine receives POM classification?
They may present a direct or indirect danger if used without medical supervision They are frequently used incorrectly They require further investigation into effects or side effects They are administered parenterally (by injection) They contain substances which activity/adverse reactions require further investigation They are new medicinal products containing a substance not included in previously authorized medicines
40
What are the storage requirements for POM medicines?
Stored in the dispensary or other secure area Kept in temperature-controlled conditions as specified by manufacturer Some require refrigeration (2-8°C) Controlled drugs (certain POMs) must be stored in a locked controlled drug cabinet Protected from unauthorized access at all times
41
What is the legal framework governing medicine classification in the UK?
The Medicines Act 1968 and subsequent Human Medicines Regulations 2012 provide the legal framework. The MHRA (Medicines and Healthcare products Regulatory Agency) oversees medicine classification, with the Commission on Human Medicines advising on changes to legal categories.