PRESCRIPTION
Ms. PRIYA TIWARI
Assistant Professor
Faculty of Pharmaceutical Sciences
Rama University
Kanpur
CONTENTS
INTRODUCTION OF PRESCRIPTION
PARTS OF PRESCRIPTION
TYPES OF PRESCRIPTION
LEGAL REQUIREMENT FOR VALID PRESCRIPTION
HANDLING OF PRESCRIPTION
ERROR IN PRESCRIPTION
ABRIVIATIONS
INTRODUCTION
 It is an order written by a physician, dentist,
  veterinarian or a registered medical practitioner
  (RMP) to a pharmacist to compound and dispense a
  specific drug for the patient. OR
 Prescription is a written order for medication, issued
  by physician or RMP. Prescription is relationship
  between physician and pharmacist.
Physician (RMP)          Pharmacist      patients
Cont…
 The word "prescription" is derived from the Latin
  term praescriptus.
    (Prae - 'before' and scribere- meaning 'to write').
 Prescription means 'to write before' which means
  prescription had to be written before a drug could be
  compounded and administered to a patient.
PARTS OF A PRESCRIPTION
A typical prescription consists of the following parts:
 1. Prescriber office information
 2. Date
 3. Patient information (Name, Age, Sex And Address Of The Patient)
4. Superscription (symbol ℞)
5. Inscription (Medication prescribed)- Main part of prescription
6. Subscription(Direction to Pharmacist/Dispenser )
7. Signatura or Transcription (Direction for Patient)
8. Renewal instructions
9. Prescriber’s signature and registration number.
1.Physician (Prescriber) office Information:
     Information about physician is essential so that the patient
     could be contact in emergency. Following information is
     mentioned on the prescription
i.     Doctor's or office name.
ii.     Address with phone number and e-mail.
iii. Prescription number, (required when calling the
       pharmacy for a refill)
2. Date
It helps a pharmacist to find out the date of
  prescribing.
It also helps in know when the medicines were last
  dispensed if the prescription is brought for
  redispens.
In case of habit forming drug the date prevents
  the misuse of the drug by the patient
3. Patient information
PATIENT INFORMATION (Name, Age, Sex and
 Address of the Patient)
Name and address of the patient for identification
 purpose.
Age and sex of the patient is required for child
 patient to check the prescribed dose.
4. SUPERSCRIPTION (symbol ℞)
It is represented by ℞ (Latin term) „recipe‟ which
  means „take thou‟ or „you take‟.
 In olden days, the symbol was considered to be
  originated from the sign of Jupiter.
Jupiter is the Greek God of healing.
 This symbol was use for requesting God for the quick
  recovery of the patient.
5. INSCRIPTION (Medication prescribed)
 It is the main part of the prescription.
 It contains the names and quantities of the prescribed
   medicaments.
The medicament may be official preparation or nonofficial
   preparation.
a.) Official preparation (i.e. from pharmacopoeia) – Only
   name of the preparation is written E.g. Piperazine Citrate
   Elixir IP
b.) Nonofficial preparation- Quantity of each ingredient
   will be given and type of preparation will also be given
6. SUBSCRIPTION (Direction to Pharmacist)
 In this part the prescriber gives direction to the
  pharmacista) Regarding the dosage form to be
  prepared.
 b) Number of doses to be dispensed.
7. SIGNATURA (Direction for Patient)
To be placed on the label.
It is usually written as „Sig.‟.
The signatura written in english and use some
 Latin abbreviations like t.i.d (thrice a day),
 b.i.d (twice a day) and o.d (once a day).
Cont..
Instructions should be written on the label of container so that
  the patient can follow them.
The instructions may include-
a) Quantity to be taken(dose of drug)
b) Frequency and timing of administration of the preparation
  (dose interval)
c) Route of administration
d) Special instruction (if any)
8. RENEWAL INSTRUCTIONS
The number of times a prescription is to be repeated is
 written by the physician.
It is very important for the case of habit forming drugs
 to prevent its misuse.
9. PRESCRIBER’S SIGNATURE AND
REGISTRATION NUMBER
The prescription must be signed by the prescriber by
  his / her own hand.
 Registration number should be written in the case of
  dangerous and habit forming drugs.
TYPES OF PRESCRIPTION
Prescriptions can be classified as
             a) Compounded prescription
          b) Noncompounded prescription
a). Compounded prescription-
Also known as extemporaneous prescription.
 It is an order that requires mixing of one or more
  ingredients (active medicaments).
It contains several ingredients which are divided into
  the following parts:
(a) Base: The active medicaments (Produce the
    therapeutic effect).
(b) Additives-1) It enhances the action of the drug.
Cont…
2) It makes the preparation more elegant (attractive)
  and palatable.
(c) Vehicle: It is the main carrier of the drug. E.g. -In
  liquid preparations solvent (water) used as vehicle.
 Now a day’s compounding is omitted from
  prescription.
E.g.       Sodium bicarbonate -3g
                  Simple Syrup -6ml
           Purified Water (q.s.)- 100ml
b).Non-compounded prescription
Does not require compounding of pharmaceutical
 product.
Precompounded drugs supplied by a pharmaceutical
 company by its official or proprietary name.
Legal Requirements for a Valid Prescription
1. Prescription should be written in indelible (can not
   erased) ink (may be handwritten or computer
   generated)
2. Prescription must be signed in indelible ink by the
   practitioner using his own name.
3. Prescription must be dated by the prescriber.
4. Prescription should state address of the practitioner
5. if issued by a dentist the words „for dental use only
Cont…
 6. Prescription always writes legibly.
 7. Prescription always space out words and numbers
 to avoid confusion.
 8. Prescription always contains complete medication
 orders.
 9. Avoid abbreviations.
CONT…
Now a day’s electronic prescriptions use, to minimize
medication errors.
The use of Latin word in prescription writing is
traditional.
Now a day’s Latin has slowly gone.
example
Latin Terms Latin term / phrases
Abbreviation
Semel in die or omne in      o.d.         Once a day
          die
   Bis in die, Bis die       b.d          Twice a day
   Ter in die, Ter die       t.i.d        Thrice a day
     Quartar in die       q.i.d., q.d   Four times a day
      Si opus sit           s.o.s       When required
HANDLING OF PRESCRIPTION
The following procedures should be adopted by the
   pharmacist while handling the prescription for
   compounding and dispensing:
 I. Receiving
II. Reading and checking
III. Collecting and weighing the materials
 IV. Compounding, packaging and labeling
I. Receiving
The prescription should be received by the pharmacist.
 While receiving a prescription, a pharmacist should
 not change his/her facial expression.
  It gives an impression that he/she is confused or
 surprised after seeing the prescription.
II. Reading and checking
After receiving the prescription it should be screened
  behind the counter.
Prescription authenticity should be checked.
The signature of the prescriber and the date of prescription
  should be checked.
The pharmacist should read all the lines and words of the
  prescription.
He/she must not guess any word.
If there is any doubt, the pharmacist should consult with
  the other pharmacist or the prescriber over telephone.
(III). Collecting and weighing the material
Before compounding a prescription all the materials
  should be collected from the shelves or drawers.
 All the materials kept in the left hand side of the
  balance. After measuring each material should be
  kept on the right hand side of the balance.
Cont…
After compounding of the prescription materials are
 replaced back to the shelves / drawers. While
 compounding every container of material should be
 checked thrice in the following manner:
(i) When collected from the shelves/drawers.
(ii) When the materials are measured.
(iii) When the containers are replaced back to the
 shelves/drawers.
IV. Compounding, packaging and labeling
Only one prescription should be compounded at a time.
 Compounding should be done on a clean table.
All equipment required should be cleaned and dried.
 The preparation should be prepared according to the
 direction of the prescriber or as per methods given in
 pharmacopoeia or formulary.
The compounded preparations should be filled in
 suitable containers.
Label the container.
CARE REQUIRED IN DISPENSING PRESCRIPTION
 1.The prescription must be carried with the pharmacist while taking the
 medicine out of the shelves.
 2.The dispensing balance should always be checked before weighing any
 ingredient.
  3.All the chemicals should be replaced back in to their original positions in the
 shelf.
 4.Care should be taken to keep the balance clean after each measurement.
 5.Liquid preparations for external use the label must display FOR EXTERNAL
 USE ONLY in red ink
 6.Before handing over the medicine to the patient, again the preparation should
 be checked.
1. Abbreviation
In most of the prescriptions abbreviated terms are used
 by the prescriber that leads to major errors during
 interpretation by the pharmacists. E.g. „SSKI‟ is the
 abbreviated term of „Saturated Solution of Potassium
 Iodide‟.
It is preferable to avoid these types of misleading
 abbreviations.
2. Name of the drugs
Names of some drugs (especially the brand
 names) either look or sound alike. So any error
 in the name of a drug will lead to major danger
 to the patient. e.g. Althrocin – Eltroxin, Acidin
 – Apidin , Digoxin- Digitoxin etc.
3. Strength of the preparation
Drugs are available in the market in various strengths.
 So a drug must not be dispensed if the strength is not
 written in the prescription. E.g. Paracetamol tablet
 500mg should not be dispensed when no strength is
 mentioned in the prescription.
4. Communication failure
 Failures during the process of patient management -
 Includes    illegible   handwriting,    incomplete
 prescribing order. Common errors include: „g‟
 mistaken for „mg‟
5.Dosage form of the drug prescribed
Many drugs are available in more than one dosage
 forms. E.g. liquid, tablets, injections or suppositories.
 The dosage form intended for the patient must be
 mentioned in the prescription to reduce ambiguity.
6.Dose
If unusually high or low dose is mentioned in the
 prescription then it must be consulted with the
 prescriber. Some time a sustained release (SR) dosage
 form is prescribed thrice or more times daily.
 Actually SR dosage forms should be given once or
 twice a day.
7.Instructions to the patient
 Some times the instruction for a certain
 preparation is either omitted of mentioned
 partially. The route of administration should be
 mentioned clearly.
8. Incompatibilities
It is essential to check that there are no pharmaceutical
  or therapeutic incompatibilities in the prescription. If
  more than two medicines are prescribed then it is the
  duty of the pharmacist to see whether their
  interactions will produce any harm to the patient or
  not. Certain drugs have interactions with food. E..g,
  Tetracycline should not be taken with milk or antacid.
LABELING OF DISPENSED MEDICINES
 After dispensing the medicine in a container, a label is
  attached by adhesive. The label on the dispensed
  medicines      should   provide     the     following
  information:–
1. Name of the preparation-
   When the prescriber mentions the name in the
    prescription the same name must be displayed on
    the label.
Example
 PIPERAZINE CITRATE ELIXIR IP
 If it is a non-official preparation then the name of the
 dosage form should be given on the label.
 e.g. THE MIXTURE, THE EMULSION, THE
 DUSTING POWDER
Cont…
2. The strength of the medicine-
  The strength of the active ingredient in the
  preparation must be displayed if it is intended for
  internal (oral) purpose. The amount in each unit of
  dose should be mentioned.
  e.g. In case of oral liquids “Each 5ml contains
  250mg”
 e.g. In case of tablet “Each tablet contains 500mg”.
Cont..
 The values must be written in whole numbers and if
 decimal is not avoidable then a zero is placed before
 the decimal point. E.g. instead of 0.1g it should be
 100mg, and instead of .5% it should be 0.5%. In case
 of an official preparation the strength is not required
 to be given, because the name with reference to the
 pharmacopoeia is sufficient.
 E.g. CHLORAMPHENICOL ORAL SUSPENSION
 IP.