Exercise No 2
Exercise No 2
Exercise No 2
2
MEDICATION ORDER AND DRUG LABELS
I. OBJECTIVES
1. To master the meaning of latin abbreviations used in the medication order.
2. To be able to interpret the labels of the medications.
II. DISCUSSION
MEDICATION ORDER
Prescription is an order of medication issued by a physician, dentist, veterinarian, or other
properly licensed medical practitioner. It contains the following information; patient’s name,
name of the drug, the dose, route of administration, and frequency of administration. In a
hospital setting, the forms are somewhat different and they are referred to as medication order.
Frequency:
a.c. before meals q.i.d four times a day
p.c. after meals min. minute
ad. lib. As desired, freely h hour
p.r.n. when necessary q.h. every hour
h.s.* hour of sleep, at bed time q.2h every two hours
stat immediately, at once q.3h every three hours
q.d.* once a day, everyday q.4h every four hours
q.o.d.* every other day q.6h every six hours
b.i.d. twice a day q.8h every eight hours
t.i.d. thrice a day q.12h every twelve hours
MISCELLANEOUS ABBREVIATION:
AMA against medical advice
ASAP as soon as possible
BP blood pressure
BPM breaths/beats per minute
D/C or dc discontinue
KVO keep vein open
NKA no known allergies
P pulse
R respiration
DRUG LABELS
Drug labeling refers to the printed information that accompanies a drug, including the label, the
wrapping and the package insert. Drug labeling is regulated by the Food and Drug
Administration (FDA). This regulation applies to prescription drugs, over-the-counter (non
prescription) drugs, and dietary supplements.
The FDA requires that drug labeling be balanced and not misleading. The label must be
scientifically accurate and provide clear instruction to health care practitioners for prescription
drugs and to consumers for over-the-counter drugs and supplements. Labeling regulations
require that the statement of ingredients must include all ingredients, in order in which they are
used in the drug. These ingredients must also be identified by their established name.
The Generic Name of the drug must be identified in all drug labels. Some Brand Names are
followed by the ® sign, meaning the name is registered occasionally; only the Generic name
appears.
Other pertinent information included in drug label is as follows;
1. Therapeutic use of the medication
2. Potency/Dosage Strength-weight of the active drug
3. Dosage Form-tablet, capsule, powders, suspension, solution, etc.
4. Supply Dosage- dosage strength ad form which usually reads together
e.g. 20mg/mL; 100,000 USP Units ML
5. Total Volume- of liquid in containers
6. Indication
7. Administration Route- like oral, sublingual, injection, rectal, vaginal, IV, IM use. (Unless
otherwise specified, tablets, capsules, and caplets are intended for oral use)
8. Direction for reconstitution/mixing- for powdered form of drugs
9. Name of the manufacturer
10. Expiration Date- medications should either be used or discarded, or returned to the
pharmacy by this date
11. Lot and registration number
Before dispensing the drug, the pharmacist should compare the order and label; the secret to drug
safety is to CHECK and CHECK AGAIN. He should carefully compare the drug’s label with
each part of the medication administration record and hold the label next to the administration
record to ensure accuracy
The following are reminders to a pharmacist before a drug is given, e.g. Furosemide (Lasix)
40mg P.O. tablet.
3. Check drug names
Read the drug’s generic name on the administration record and compare it to the generic
name on the label. They both should indicate furosemide
Exercise No. 2
Medication Order and Drug Labels
Interpret the Medication order and provide the information needed below.
LNU HOSPITAL
Mendiola, Manila
DATE TIME A.M. Rm.101 10/25/10
10/27/10 10 P.M Cristina Diaz
12-14-60
Matimtiman St. CARITAS
Diabenese 0.1g po qd ac breakfast Malolos City ROMAN CATHOLIC
ORDERS NOTED:
Date: 10/27/10 Time: 10:05 am
Nurses signature: ________________
_____________________________________________________________
Identify the information requested:
Label A:
Manufacturer: _______________________________________________________________
Label B:
Generic Name: _______________________________________________________________
Brand Name: _________________________________________________________________
Dosage Strength: ______________________________________________________________
Quantity of Drug: ______________________________________________________________
Expiration Date: _______________________________________________________________
Special Instructions: ____________________________________________________________
Auxilliary label: _______________________________________________________________
Total dose to be given to a child per day: ____________________________________________
Label C:
Manufacturer: _______________________________________________________________
Label D:
D. Generic Name: ____________________________________________________________
Manufacturer: _______________________________________________________________
b. Expiration Date
c. Route of administration
d. Manufacturer
3. What is/are the effect(s) on the drug and on the patient if the instructions for storage
conditions were not followed?