Guidance on prescribing Flashcards

1
Q

Do biologics need to be prescribed by brand name and if so why?

A

> Yes and automatic substitution of brands at point of dispensing is not appropraite
Size, complexity and way they are produced can result in a degree of natural variability

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2
Q

What information is important when reporting adverse reaction to yellow card scheme for biologic meds?

A

Brand name and batch number

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3
Q

Is it appropriate to abbreviate titles of drugs?

A

No- in general should be written in full to avoid misinterpretation

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4
Q

Is it appropriate to use generic names in prescribing?

A

> Yes- and they should generally be used to allow any suitable product to be dispensed- saving delay
Unless there is difference in clinical effect between manufacturers and brand name is needed (e.g. Qvar vs Clenil)

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5
Q

When should an oral syringe be given?

A

When oral liquid med prescribed in doses other than multiples of 5–> if Rx in 5ml doses then spoon given

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6
Q

What constitutes a ‘sugar-free’ oral liquid prep?

A

> Liquids that don’t contain fructose, glucose sucrose

> Also those that have hydrogenated glucose syrup, mannitol, maltitol, sorbitol or xylitol

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7
Q

Why is the presence of benzyl alcohol in injections indicated in the BNF?

A

It has been associated with fatal toxic syndrome in preterm neonates

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8
Q

Why is the presence of polyoxyl castor oil in injections indicated in the BNF?

A

It has been associated with severe anaphylactoid reactions

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9
Q

Why is the presence of propylene glycol in oral or parenteral meds indicated in the BNF?

A

> It can cause adverse effects if elimination impaired e.g. renal failure, neonates, young children and slow metabolisers
Can also interact with disulfram and metronidazole

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10
Q

At what sodium level is a medicine considered ‘sodium-free’?

A

<1mmol per dose

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11
Q

At what sodium level is a medicine considered ‘high-sodium’?

A

> 17mmol per dose (this is about 20% of total daily recommended WHO amount)

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12
Q

What are the requirements if extemporaneous product needs to be made in absence of authorised product?

A

> Must be ‘freshly prepared’ (i.e. not more than 24hrs before use)
Should be used within 4 weeks if stored at 15-25C
Fresh clean water should be used (either from tap or boiled and cooled)

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13
Q

What do prescribers need to tell patients when given them meds that can impair driving?

A

> Let them know it will likely affect driving
Warn them of potentiating effects with alcohol
Advise them to carry evidence to show med was Rx and not illegal with instructions of how it’s taken

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14
Q

When can a med not be put in a child-resistance container?

A

> Med is in original packet
Patient won’t be able to open child resistant container
Specific request made not to have it in child-resistant container
No suitable container available

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15
Q

What is legally required to appear on dispensing label?

A
  1. Name of patient
  2. Name and address of pharmacy
  3. Date of dispensing
  4. Name of med
  5. Directions for use
  6. Precautions relating to use of med
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16
Q

What is ‘recommended’ by RPS appears on label?

A
  1. ‘Keep out of sight and reach of children’

2. Use medicine only on your skin

17
Q

Can pharmacists dispense Rx’s from EEA or Switzerland and if so what are the limits?

A

Yes- except Sch 1, 2, 3 or ones without UK marketing auth