Prescriptions E-learning and other Flashcards

1
Q

Aseptic meaning:

A

free from contamination caused by harmful bacteria, viruses, or other microorganisms.

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2
Q

What are Medicines Policies and what are the four aims of it?

A

Four aims are:
- Principle: to highlight principles by which drugs are to be stored, supplied, transported and administered within a clinical setting and so closely reflect the HMR 2012
- People: aim to ensure all members of staff are aware of their roles, responsibilities and limitaations with respect to medicine
- Audit: aim to ensure an auditable trail for the handling of medicines including controlled drugs
- RIsk management: aim to help manage the risks that drugs can pose to patients, service users, residents and staff to ensure users recieve appropriately prescrived medicine safely and effectively

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3
Q

NHS hospitals

What is an Inpatient Drug Chart?

A

An ‘order’ for the administration of drugs to a patient. You would use these charts to document the drug treatement to be given to a patient during their inpatient stay. They are subject to regulations and standards of code.

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4
Q

NHS hospitals - Discharge summary

What are TTOs and TTAs

A

TTO (to take out) and TTA (to take away) are used to prescribe medication to be given to inpatients on discharge. You would prescribe sufficient medication to allow time for the discharge summary to reach the patient’s GP for medication to be continued. Recommended duration is 14 days.

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5
Q

How to know if a drug is controlled?

A

Schedule 2 and 3 preparations are identified by the symbols CD2 and CD3 respectively next to the drug in the BNF - You can also find it in Controlled drugs and drug dependence in the BNF

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6
Q

NICE guidance on controlled drugs

What to do when prescribing CDs

A
  • Document the indication and dosing regimen in the patient’s medical records
  • Assess the patient’s current clinical need and adjust prescription as appropriate
  • Discuss with the patient how their treatment will be reviewed and monitored.
  • Be able to discuss prescribing decisions with other HPs if required

Remember to tell their GP bout this

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7
Q

NICE guidance on CDs

What to do for ‘when required’ CDs

A
  • Document clear instructions for when and how to take or use the CD in the patient’s medical notes.
  • Annotate the dosage instructions on the prescription ie maximum dose and frequency
  • Consider any pre-existing supplies of the CD the patient may have at home before supplying on discharge

Remember to tell their GP bout this

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8
Q

NICE guidance for prescribing CDs

What to do when reviewing or amending a CD prescription

A
  • Adhere to local and national guidance when you prescribe, review or amend a CD prescription and take into account:
  • the apppropriate route
  • dose
  • formulation
    Clearly document any deviations from prescribing guidance in the patient’s medical notes.

Remember to tell their GP bout this

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9
Q

NICE guidance for prescribing CDs

What to do when needing to prescribe multiple routes of administration?

A
  • Prescribe each route as a separate item
  • Clearly document on the prescription when each route can be used
  • CLearly cross-reference to prevent any accidental overdose by dual administration via both routes

Remember to tell their GP bout this

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10
Q

What does GSL, P and POM mean

A

GSL (General sales list)- drugs available for general sale
P (Pharmacy medicines) - Drugs restricted to sale through pharmacies
POM (Prescription only medicines) - Prescribed by practiioners only. CDs included can only be prescribed by practitioners and restrictions apply to some NMPs

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11
Q

What is meant by an unlicensed medicine?

A

Medicines that have not been subject to the licensing process so doesn’t have a uK Marketing Authorisation from the MHRA. This may include:
- Clinical trial drugs
- Drugs awaiting MHRA approval
- ‘Specials’ products made specifically for a given purpose and sometimes a named patient
- A drug licensed in another country other than the UK.

The HMR allows for unlicensed drugs to be used if licensed ones aren’t available and the patient needs it

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12
Q

What is meant by off-label prescribing?

A

Drug that is licensed in the uK but is being used outside the terms of its Marketing Authorisation E.G
- Drug licensed only in adults which is being used for a child (e.g lansoprazole)
- Drug used for an indication not stated in the Marketing Authorisation
- Drug administered via a route other than stated in the licensed way.

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13
Q

Good practice in prescribing unlicensed or off-label drug, what to check?

A
  • Be satisfied that there are no suitable licensed alternatives that would meet the patient’s clinical needs
  • Be satisfied that there is sufficient evidence base and/or experience for its use
  • Be prepared to take responsibility for prescribing and overseeing the patient’s care (including monitoring)
  • Document your decision in the medical notes, including the rationale for the precription
  • Make sure that off-label is approved (indicated in the BNF)
  • Only prescribe unlicensed drugs with advice from and under the supervision of a senior clinician
  • Inform your patient and gain consent where possible for the used of the drug
  • Some medicines are routinely used outside the terms of their license. In this case it may be sufficient to describe why the drug isn’t licensed for the proposed use or patient.
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14
Q

What to do when reviewing prescriptions?

A
  • REview all medicaiton regularly
  • Stop any unnecessary medicine
  • Consider documenting review dates, both within the patient’s notes and on the inpatient charts
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15
Q

What to do when cancelling a prescription on an inpatient drug chart?

A
  • Cross through the entire entry
  • Annotate the entry with your signature and a date
  • Do not obliterate the entry in its entirety as the medicine is still part of your patient’s medical history
  • Document any changes to your patient’s prescribed therapy in the medical notes, including the rationale for change
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16
Q

Which practitioners are permitted to prescribe with accredited postgraduate training or upon graduation?

A

Pharmacist Independent Prescribers: They can prescribe medicines in both hospital wards and clinics after completing accredited postgraduate training.
Prescribing Pharmacists: Work in specialty clinics (e.g., oncology, renal transplant) or during surgical pre-operative processes​

17
Q

What is the difference between supplementary and independent non-medical prescribers?

A
  • Independent Non-Medical Prescribers: Prescribe autonomously without doctor supervision, managing patient medications within their clinical role.
  • Supplementary Prescribers: Prescribe in partnership with a doctor or dentist, following an agreed patient care plan
18
Q

What are the legal requirements of a prescription?

A
  • Legal: Includes prescriber’s and patient’s details.
  • Safe: Considers contraindications, interactions, and allergies.
  • Effective: Evidence-based for clinical needs.
  • Rational and Practical: Appropriate for the patient, including dosage and administration​
19
Q

What are the five rights of a safe prescription?

A

Right drug
Right dose
Right route
Right time
Right patient​

20
Q

What are the types of FP10 NHS prescriptions and who is permitted to prescribe on them?

A
  • FP10NC: GPs, hospital doctors, and independent nurse prescribers.
  • FP10HNC: Hospital-based doctors and authorized prescribers.
  • FP10SS: Independent and supplementary prescribers, such as pharmacists and nurses.
  • FP10MDA: For controlled drugs, used in substance misuse cases.

Restrictions: Some drugs, especially controlled substances, are limited to specific healthcare professionals​

21
Q

How do prescriptions in secondary care differ from those in primary care?

A
  • Secondary care: Uses electronic prescribing (EP) systems with clinical decision support for complex cases requiring integration across departments.
  • Primary care: Often uses FP10 forms or simpler electronic systems for outpatient treatment with less frequent medication changes
22
Q

What are the two key components of Integrated Care Systems (ICSs)?

A
  • Integrated Care Board (ICB): Responsible for NHS services, health outcomes, and financial performance for the ICS area.
  • Integrated Care Partnership (ICP): Brings together the NHS, local government, and other providers to produce an integrated care strategy
23
Q

What is the pharmacist’s role during inpatient care?

A
  • Clinically screen inpatient drug charts.
  • Ensure safe supply of medications to clinical areas.
  • Conduct drug histories and medication reconciliations.
  • Process medications for discharge (TTOs).
  • Complete ward-based audits (e.g., controlled drugs)
24
Q

What are some responsibilities of a ward-based technician?

A
  • Undertake complete drug histories.
  • Identify discrepancies and assist with medicines reconciliation.
  • Check patients’ own drugs (PODs) for appropriateness.
  • Ensure sufficient medication supply for inpatients and on discharge.
  • Support with ward-based audits​
25
Q

What are some reasons why an accurate drug history is important?

A
  • Aid in diagnosis (e.g., indicators for specific diseases).
  • Avoid adverse drug effects.
  • Prevent masking of clinical signs.
  • Identify drug interactions.
  • Guide future treatment, including identifying beneficial or harmful medicines​
26
Q

What is the role of a hospital pharmacist during the patient journey?

A
  • Admission: Drug history and medicines reconciliation.
  • Inpatient Stay: Clinical screening of drug charts, advising on prescribing.
  • Discharge: Clinical screening of discharge prescription, patient counseling, and medication supply
27
Q

What is medicines reconciliation and its benefits?

A

Medicines Reconciliation: Ensures that patients’ medication lists are accurate and up to date when transferring between care settings.
Benefits:
* Reduces medication errors and adverse drug events.
* Prevents missed doses.
* Reduces hospital admissions/re-admissions due to medication-related harm.
* Improves communication between healthcare professionals​

28
Q

What is the role of an eP Pharmacist?

A
  • Maintaining the drug dictionary: Ensuring all medications are accurately listed and updated in the system.
  • Developing decision support: Creating tools to improve clinical decision-making and optimize treatment.
  • Developing new functionality: Enhancing the prescribing system to meet evolving clinical needs.
  • Investigating incidents: Identifying and resolving issues within the prescribing system that could affect patient safety
29
Q

What must all medicine packaging and containers be according to HMR 2012?

A

Legible, comprehensible, indelible, and provided in English.

30
Q

What are the legal requirements for packaging and labeling medicines for human use?

A

Packaging and labeling must meet HMR 2012 standards: legibility, indelibility, inclusion of specific product details (name, strength, active ingredients, usage instructions), expiry date, and appropriate warnings.

31
Q

What packaging and labeling safety features does the MHRA recommend for MA holders?

A

MHRA recommends features to minimize errors: consistent strength notation (e.g., no trailing zeros), “micrograms” spelled out, clear differentiation for drug types, full product name on at least three sides of packaging, and appropriate color use.

32
Q

How can you locate patient information leaflets (PILs), and why are they important?

A

PILs can be found on the packaging or online via MHRA resources. They are essential for educating patients on usage, precautions, interactions, and potential side effects, promoting safe medicine use.

33
Q

What is the difference between legal requirements and good practice for the packaging and labeling of prescription medicines?

A

Legal requirements (HMR 2012) mandate essential information (e.g., product name, dosage, warnings) and safety features. Good practice, guided by MHRA, includes additional labeling for clarity, such as full patient names and detailed administration instructions to enhance patient safety.

34
Q

Labelling requirements MA holders

What are all 18 requirements for medicine

A
  1. Name of medicinal product (must also be in Braille)
  2. Strength & pharmaceutical form
  3. Whether intended for babies, children or
    adults (where appropriate)
  4. Active substance common name
    (for up to 3 active substances)
  5. Qualitative & quantitative expression of the
    active substance (common name) per
    dosage unit or for a given volume or weight
  6. Pharmaceutical form & contents by
    weight, volume or number of doses
  7. The method of administration
  8. Where appropriate, space for the
    prescribed dose to be indicated (i.e.,
    POMs require space for a dispensing label)
  9. A warning that the product must be
    stored out of the reach & sight of children
  10. Any applicable special warnings
  11. Any applicable storage precautions
  12. Expiry date (month and year)
  13. Manufacturer’s batch number (lot no.)
  14. Name & address of MA holder
  15. Marketing Authorisation number
    (Product licence no.)
  16. Legal category if P or POM and if not
    a POM, instructions for use
  17. Any special disposal precautions
  18. A list of
    A) all excipients for injectable, topical or eye products
    B) in any other case, excipients with a recognised
    action or effect
35
Q

Whaat are the requirements for MA Holder leaflets

A

▪ Name of medicinal product
▪ Strength & pharmaceutical form
▪ Whether intended for babies, children or adults (where appropriate)
▪ Active substance common name (for up to 3 active substances)
▪ Drug pharmaco-therapeutic group or type of activity (lay language)
▪ Therapeutic indications
▪ A list of
− Contraindications (e.g., pregnancy, breastfeeding)
− Precautions
− Interactions (medicines and other substances)
− Special warnings (e.g., possible effects on ability to drive & operate machinery)
▪ Instructions for use (e.g., dose, route, frequency etc)
▪ Adverse reactions (i.e., ALL known side-effects in descending order of frequency)
▪ Reference to expiry date, storage requirements, active ingredients &
excipients, name & address of MA holder, name & address of manufacturer
▪ Information on adverse event reporting
▪ Date last revised
▪ Additional requirements for
− Paracetamol, codeine & dihydrocodeine products (warnings)
− Radiopharmaceuticals