The Pharmacist Flashcards
P medicine and examples
Covered by authorization that it has to be available only from a pharmacy: Night nurse Contact capsules Tyrozets Chloramphenicol eye drops
Products only available from a pharmacy
Anthelmintics - for worms
Parenterals
Enemas
For irrigation or wounds, bladder, vagina or rectum
Aloxiprin or aspirin(>16) from admin to children
Examples of exemptions to POM that are P
Budesonide 200mg per nostril/ 10mg in pack Nasal admin only Prevention/treatment of hayfever Adults and children >12
Econazole
Vaginal candidiasis - vaginal use
Chlorine phosphate
Prophylaxis of malaria
Some controlled drugs if: One Specified max strength in form specified labelled to show dose
Liquid paraffin GSL and P differences
GSL = all P = nasal drops, sprays, inhalation’s, oral laxatives
Quinine classes POM ,GSL and P differences
POM
P = MD 100mg and MDD 300mg
GSL = MD 35mg
Cetrizine Hydrochloride GSL and P differences
P =MDD 10 mg
GSL = 30 tabs or 70ml of 1mg/ml (still 10mg MDD)
Beclometasone classes POM, GSL and P differences
POM=nasal spray
P=allergy nasal spray
GSL=Hayfever nasal spray
Aspirin GSL pack sizes
0-325mg 30 tablets
Up to 500mg 20 tablets
Non effervescent
Up to 75mg e/c, ONLY aspirin 28 tablets
Others 16 tablets
Paracetamol GSL pack sizes
Capsules 16
Powder or granules 10 sachets
Liquids for over 12’s is 160ml
Liquids for under 12’s is 100ml
Ibuprofen GSL pack sizes
16 tablets
16 capsules
12 sachets
100ml
What is criminal law
Between the individual and state
Regulation of human behaviour
What is penal law
Bodies of rules with the potential for severe impositions as punishment for failure to comply
What is civil law
Relationships between individuals (or a large organisation)
Compensation
Private disputes
Protects and enforces rights of an individual
Do pharmacists need professional indemnity insurance?
Yes - required by GPhC
What is a Primary Legislation?
Acts or parliment
Lay down general principles
No great detail
Examples of primary legislation?
Medicines act 1968
Misuse of drugs act 1971
Poisons act 1972
What is a secondary legislation?
Subsidiary to an act
Normally in the form of statutory instruments
Include regulations and orders
Who initiates a statutory instrument?
A government minister
When does a statutory instrument become law?
After laying on the table for 3 days
What do an act and a statutory instrument form?
Statutory law
What is Judicial Precedent?
Case law/common law/judge-made law
When no legislation on issue
Legislation is unclear
Statement of the legal position in a case based on previous courts decisions/similar cases
Who is the European union made up of and what are their roles?
European commission - initiates
Council of EU - makes ultimate decisions
European Parliament - directly elected chamber
European court of justice - Decisions by them must be accepted by courts in member states and there is no right of appeal
What are specified publications under HMR 2012
European Pharmacopoeia
British Pharmacopoeia
Cumulative list of recommended INN’s
What do the MHRA do
set standards for the quality of medicines
Ensure medical substances meet standards of safety, quality and efficacy
Ensure medicines and medical devices work and are acceptably safe
What is found in the monograph
Description Identification tests Physical constants Min purity Ingredients Limit tests Storage conditions
How is public protection achieved
Restricting public access to poisons and potent drugs/medicines
Prevent use for criminal purposes, self medication and gratification of addiction
What is the CHM
Commission on Human Medicines
Committee of MHRA - advise ministers
Advisory non-departmental public body
Membership - clinicians, pharmacists, lay members, expert advisory groups
What is a medicinal product
A substance or combination that has properties of preventing or treating disease in humans
Administered to:
Restore/correct/modify a physiological function by exerting a pharmacological/immunological/metabolic action
Make diagnosis
What is a authorised medicinal product
Medicine - marketing authorisation
Homeopathic’s - Certificate of registration
Herbals - Traditional herbal registration
What is a relevant medicinal product
A medicinal product with a marketing authorisation
What is a medicinal purpose
Treating/preventing disease
Diagnosing or ascertaining existence/degree/extent
Contraception
Anesthesia
Preventing or interfering with the normal operation of physiological function
When are medicinal products usually designated POM
Medical supervision require to prevent (in)direct damage to human health
Misused and danger
New active substance
For parenteral admin
Who can prescribe all POM’s
Doctor Dentist Pharmacist IP Nurse IP Supplementary prescriber
Who can supply restricted POM’s
Optomestrist IP Paramedic IP Physiotherapist IP Podiastrist IP Therapeutic Radiographer IP Community practitioner nurse prescriber
What can Optometrist IP’s prescribe
Any POM
No CD’s or parenterals
What can Chiropodist IP’s prescribe
Any POM Diazepam Dihydrocodeine Lorazepam Temazepam
What can Physiotherapist IP’s prescribe
Any POM Diazepam Dihydrocodeine Lorazepam Temazepam Fentanyl Oxycodone Morphine
What can Therapeutic radiographer IP’s prescribe
Any POM Codeine Fentanyl Morphine Oxycodone Tramadol Midazolam Temazepam
What can Paramedic IP’s prescribe
Any POM Codeine Fentanyl Midazolam Morphine
Community practitioner nurse prescriber can prescribe
Certain POM's - licensed with marketing authorisation Co-danthramer (caps, oral) Co-danthrusate Mebendazole Miconazole Nystatin Streptokinase and streptodornase topical powder Water for injections Dressing/appliances
What is supplementary prescribing
Voluntary partnership between doctor or dentist and a supp prescriber to implement an agreed PATIENT SPECIFIC clinical plan with patients agreement
Who can be a supplementary precriber
Pharmacist Registered midwife Registered nurse Chiropodist/Podiatrist Paramedic Physio Radiograoher Registered optom Registered dietician
What should a clinical management plan include
Name of patient Illnesses/conditions to be treated by SP Date of effect and review by IP Class of description of medicinal product Restrictions/limitations - strengths, doses, period of use Relevant warnings/patient difficulties Reporting or suspected/known ADR's When SP should seek IP help
Which drugs can be prescribed by supplementary prescribing?
Meds referred to in clinical management plan: GSL and P Appliances/devices Foods Borderlines All POM inc parenteral CD's Off license Unlicensed drugs as part of clinical trial
Is an EEA/Switzerland prescription valid in the UK?
Yes except CD 1-3
Must be a doctor, nurse (gen care), dentist, midwife, pharmacist, registered in the EEA or Switzerland
A valid UK rx must contain…
Patient name Patient address Patient age if under 12 Prescriber signature Prescriber particulars Prescriber address Appropriate date (7)
What is a repeatable prescription?
Contains direction that it may be dispensed more than once
Only PRIVATE
When must the first repeat of a POM repeatable prescription be done by?
Within 6 months of appropriate date
CD4=28 days
How many repeats of a repeatable prescription can be done if not specified?
One (so original then another)
For oral contraceptives = 5 times (so 6 altogether)
After the first repeat of a repeatable prescription, how long is it valid for?
There is no time limit unless specified
What are the requirements for EEA/Switzerland prescriptions?
Patients name, nurname, DOB (no address)
Prescriber name, surname, qualifications
Direct contact details - email, phone/fax (with international prefix), work address and country
Medicine details - name/brand, form, quantity, strength, dosage
Prescriber signiture
Date of issue - valid for 6 months
Green prescriptions
FP10NC GP Community practitioner nurse prescriber SP Hospital unit
Blue precription
FP10MDA (Installment) GP IP SP Hospital unit
Lilac Prescription
FP10P
Community practitioner Nurse Precriber
Nurse IP/SP
Yellow Prescription
FP10D
Dentists in primary care - only DPF list
Why is a fax not legally valid?
Not written in indelible ink
Not signed by appropriate practitioner
Can medicines be dispensed of a fax/ when can they be?
No - supply can only be made legally when original Rx has been received and checked
Steps to take when suspecting forged prescription
Scrutinise signature - check against known if possoble
Confirm details with prescriber (that this was what they intended)
Use contact details from directory ect , NOT prescription
When is an Electronic prescription valid?
Created in electronic form
Electronic signature - uniquely linked, identifies, can maintain, change is detectable
Sent to the person dispensing as an electronic communication
What are the laws around SUPPLY of POMs in hospitals ?
May be supplied against a written direction (PSD) of an appropriate prescriber
Prescription requirements not required - must be pateint specific
Permits sale/supply against a bedcard and patient notes
What are the laws around ADMIN of POMs in hospitals ?
Directions do not need to be in writing (Good practice)
Some have policies
Emergency requires 2 nurses checking each other
Carefully consider and agree
When does a POM record not need to be made?
NHS
Oral contraceptives
Already in CD register
Sale by wholesale dealing with order/invoice retained for 2 years
When must a POM record be made within?
How long should it be kept for?
That day or the following day
2 years
What should be in the POM record?
Patient name and address Prescriber name and address Date on prescription Date of supply Medicine details - name and quantity (form and strength if not apparent from name)
What is the fate of POM prescriptions?
Retain for 2 years
Unless:
NHS - sent off
Private CD 2/3 - Sent off
When can a pharmacist make changes to a prescription?
Name or common name of product
Directions for use
Precautions
Dose/duration (keep within cieling/timeframe)
What must be on a label of a broken bulk medicine?
Name of med Quantity in container Quantitative particulars of medicine Handling and storage requirements Expiry date Batch ref no.
What does a ‘use by’ or ‘use before’ date mean?
Product should be used before end of previous month
What does an expiry date mean?
Product should not be used by the end of that month
What conditions are needed in order to sell P meds?
GPhC registered pharmacy
Responsible pharmacist
Person selling/supplying = pharmacist or under pharmacist supervision