Internship Exercises 8-10
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Transcript of Internship Exercises 8-10
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By: Nelson T. Tubon; B.S. Pharm.; B.S.S.Ed; R.Ph.;M.S. Pharm.;Ph.D. B.M.
INTERNSHIP 1
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Exercise 8
Labeling Prescription
and Medications
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Key Terms
Labeling- means all labels and other
written, printed or graphic matter (1)
upon any article or any of its
containers or wrappers (2)
accompanying such articles
Outer labelmeans the label on or
affixed to the outside package of anarticle. Examplecarton label
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KeyTerms
Principal display panelmeans the part of
the label that is most likely to be displayed,
presented, shown, or examined under
customary conditions of display for retail sale Cosmeticsmeans articles intended to be
rubbed, poured, sprinkled, or sprayed on,
introduced into or otherwise applied to the
human body or any part thereof for cleansing,beautifying, promoting attractiveness, or
altering appearance
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Key Terms
Auxiliary labelsare placed on drug productcontainers to give the patient, healthcareprovider important information needed forusing the product
Labelmeans a display of written, printed orgraphic matter upon any article or any of itscontainer or wrappers or attached to oraccompanying such article
Inner labelmeans the label on or affixed toan immediate container
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Inpatient
Label of single unit packages should include
1. name of the drug
2. route of administration, unless oral3. strength, if applicable, volume of the product,
expressed when possible in the metric system
4. control number and expiration date
5. if repackaged, identification of the repackager
6. special storage conditions, if needed
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Multiple dose
1. identification of the dispensing
pharmacy
2. patients name
3. date of dispensing
4. name of the drug
5. strength
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Auxiliary labels
Shake well
Keep in the refrigerator, Do not Freeze
Do not use after
Refrigerate, Shake well, Discard After
External Use Only
May cause drowsiness; Alcohol and Operating Car or Machine Warning Do not Drink Alcohol
Avoid Sun Exposure
Take with food
Take on an Empty Stomach
Finish all this medication
Do not take Aspirin Keep Out of the Reach of Children
This prescription May be Refilled _____________ Times
Cancer Chemotherapy, Dispose of Properly
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Terms generally employed in
storage labeling
1. Cold20C to 80C
2. Cool80C to 150C
3. Room temperature200C to 250C
4. Warm300C to 400C
5. Excessive heatabove 400C
6. Protection from freezing
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By: Nelson T. Tubon; B.S. Pharm.; B.S.S.Ed; R.Ph.;M.S. Pharm.;Ph.D. B.M.
INTERENSHIP 1
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Exercise 9
Drug Labels and
Packaging
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KEY TERMS
Active Ingredientmeans any substance
of a drug which is intended to furnish
pharmacologic activity
Strengthmeans concentration of knownactive drug substance in formulation
Brand namerefers to the proprietary,
trade name assigned to the product by the
drug establishment
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Pharmacologic categoryrefers to the
classification of the product based on its
therapeutic action as specified in the product
registration Indicationrefers to the approved clinical
use of the product based on substantial and
scientifically supported evidence of the
safety and efficacy of the drug in the givendosage form
Key Terms
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Expirationsrefers to the date after which
the product is not expected to retain its
claimed safety, efficacy and quality or
potency or after which it is not permissibleto sell, distribute or use said product
Net Contentrefers to the total
amount/quantity/number of the dosage form
in a certain container of a productexpressed in metric system
KEY TERMS
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Batchmeans a specific homogeneous
quantity of a drug or in a case of drug
produced according to single manufacturing
order during the same cycle of manufacture Lot numbermeans any distinctive
combination of letters or numbers, or both,
by which the complete history of the
manufacture, control, packaging anddistribution of a batch or lot of a drug is
determined
KEY TERMS
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Materials approved unitmeans an
organizational element having the authority
and responsibility to approve or reject raw
materials, in process materials, packagingcomponents, and final product
Generic namerefers to the identification of
drugs and medicines by their scientifically and
internationally recognized active ingredient asdetermined by the BFAD of DOH
KEY TERMS
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Mode of administrationrefers to the site
and manner the product is to be introduced
into or applied on the body
Precautionsrefers to the instructions andspecial care required in the use of product to
avoid undesired effects and to ensure the
safe and effective use of the drug
KEY TERMS
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KEY TERMS Storage conditionsrefers to the
prevailing specified range of temperature,humidity, and other environmental factorswithin optimal stability of the product isensured based on laboratory data
Date of manufacturefor products otherthan biological products means the date(month and year) during which theprocessing of the product, from which thegoods are to be filled, is completed
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POWDERS for external use are usually
described as dusting powders, usually
contain starch, talc, and zinc stearate
DRESSINGSexternal applicationsresembling ointment usually used as a
covering or protection.
CREAMSviscous liquid or semi-solid
emulsions of either the oil in water or
water in oil type
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1. D
2. J
3. G
4. I
5. A
6. C
7. H
8. B
9. E
10. F
A.Drug Packaging