MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988...

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MODULE 5 Pharmaceutics

Transcript of MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988...

Page 1: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

MODULE 5 Pharmaceutics

Page 2: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

1. RA 8203 was signed into law on:

A. September 4, 1996B. September 13, 1988C. October 4, 1996

D. September 13, 1986E. September 4, 1992

Page 3: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

2. A complete pharmacy internship program based on RA 5921 article III section 18c shall consist of at least: A. 480 hours

B. 960 hoursC. 160 hours

D. 980 hoursE. 940 hours

Page 4: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

3. This means a method of secret writing that substitutes other letters or characters for the letter intended, or transpose the letter after arranging them in blocks or squares.

A. CodeB. CipherC. Secret Keys

D. SubstitutionE. NOTA

CODE – system of words or other systems arbitrarily used to present wordsSECRET KEYS – characteristic styles or symbols kept from the knowledge of others or disclosed confidentially to only one or a few

Page 5: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

4. RA 3720 is also known as:

A. Pharmacy LawB. Consumer Act of the PhilippinesC. Food, Drugs, Cosmetics and Devices ActD. Senior Citizens ActE. Special Law on Counterfeit Drugs

Page 6: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

5. Amount of morphine subject to life imprisonment to death penalty and a fine of 500,000 pesos to 10M pesos:

A. 500gB. 50gC. 10g

D. 1gE. 20g

MARIJUANA – 500 g SHABU – 50 g

Page 7: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

6. Ratio of the weight of a substance to the weight of an equal volume of another substance taken as a standard.

A. DensityB. Specific gravity

C. Optical ActivityD. Refractive index

Page 8: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

7. Compute for the specific gravity of potassium dichromate (K2Cr2O7) if its weight t in air =5.76g and its weight in oil 3.08g. The sp.gr of the oil is 0.86.

A. 1.86B. 1.85

C. 1.87D. 1.88

Sp. Gr = [ wt. in air/ (wt. in air – wt. in oil)] x sp. Gr of oil

Page 9: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

8. Floatation method for the determination of specific gravity is based on whose scientist’s principle?

A. AristotleB. Newton

C. EinsteinD. Archimedes

Page 10: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

9. A type of hydrometer which is used to determine the alcohol strength of any liquid containing only alcohol and water.

A. Falle’s hydrometerB. Baume hydrometer

C. Thalles’ hydrometerD. Nicholson’s hydrometer

Baume hydrometer – used for liquid heavier or lighter than waterNicholson’s hydrometer – type of hydrometer with constant depth of immersion but variable weight. Other examples of such will be Fahrenheit hydrometer, Lovi’s bead

Page 11: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

10. A method of expressing concentration where in concentration is directly proportional to the moles of solute and inversely proportional to the volume of solution

A. %w/vB. %w/w

C. MD. m

M – symbol for MOLARITYm – symbol for MOLALITY

Page 12: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

11. The pH value is calculated mathematically as the:

A. Log of the hydroxyl ion (OH-) concentration.B. Negative log of the OH- concentration.C. Log of the hydrogen ion (H+) concentration.D. Negative log of the H+ concentration.E. Ratio of H+ /OH- concentration.

Page 13: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

12. Which property is classified as colligative?

A. Solubility of a soluteB. Osmotic pressureC. Hydrogen ion (H+) concentrationD. Dissociation of a soluteE. Miscibility of the liquids

Page 14: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

13. Which equation is used to predict the stability of a drug product at room temperature from experiments at accelerated temperatures?

A. Stokes equationB. Young equationC. Arrhenius equationD. Michaelis-Menten equationE. Hixson-Crowel l equation

Page 15: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

14. The pH of a buffer system can be calculated with the:

A. Noyes-Whitney equationB. Henderson-Hasselbalch equationC. Michaelis-Menten equationD. Young equationE. Stokes equation

Page 16: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

15. Based on the relation between the degree of ionization and the solubility of a weak acid, the drug aspirin (pKa 3.49) will be most soluble at

A. pH 1.0B. pH 2.0C. pH 3.0

D. pH 4.0E. pH 6.0

Page 17: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

16. Normally, how many % of water is contained in a hard gelatin capsule?

A. 8-10B. 12-16C. 20-25

D. 2-5E. 5-10

Page 18: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

17. The largest size of hard, empty gelatin capsule that can be swallowed is:

A. 00B. 000C. 1

D. 5E. 0

The smaller the number the bigger the capsule

Page 19: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

18. This chemical agent is used to render the capsule opaque

A. Titanium dioxideB. SorbitolC. Magnesium oxide

D. SilicaE. Lactose

Page 20: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

19. This is a method of preparing tablets in which the powder mixture is compacted in large pieces and subsequently broken down or sized into granules

A. Wet granulationB. Dry granulationC. Direct compression

In dry granulation, the powder mixture is slugged or compressed into large flat tablets or pellets of about 1 inch in diameter. The slugs are broken up by hand or by the mill and pass through a screen.

Page 21: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

20. The following statement/s is/are true for wet granulation method:

I. Liquid binder is added to the powder mixture to facilitate the adhesion of the powder particles

II. Over-wetting of the powder can result in granules that are too soft for proper tableting and under wetting can result in tablets that are too hard and tend to crumble

III. Granules may be dried in thermostatically controlled ovens which constantly record the time, temperature and humidity

Page 22: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

21. Amount of shabu subject to life imprisonment to death penalty and a fine of 500,000 pesos to 10M pesos:

A. 10gB. 20gC. 50g

D. 100gE. 5000g

Page 23: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

22. An ordinary prescription shall be preserved for a period of_______.

A. 5 yearsB. 1 year

C. 3 yearsD. 2 years

5 years – POISON1 year – DANGEROUS DRUGS

Page 24: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

23. When the generic name and brand name are NOT legible, this is a/an___________ prescription.

A. ViolativeB. Erroneous

C. ImpossibleD. NOTA

Impossible prescription:•Only the generic name is written but is NOT legible•Generic name does NOT correspond with the brand name•Both generic and brand name are NOT legible•Drug product prescribed is NOT registered with the BFAD

Page 25: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

24. Supplies or medicines to be given to senior citizen should not exceed

A. One day supplyB. One week supply

C. One month supplyD. One year supply

Page 26: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

25. Most biological are stored at this temperature:

A. 2 – 8°FB. 12 – 8°F

C. 2 – 8°CD. 12 – 8°C

Page 27: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

26. LAL stands for:

A. Limulus Antibiotic LysateB. Lyophilized Antibiotic LysateC. Limulus Amoebocyte LysateD. Lyophilized Amoebocyte Lysate

Page 28: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

27. The normal moisture content of hard gelatine capsules:

A. 2 -5%B. 12 – 16%

C. 20 – 24%D. 25 – 30%

Page 29: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

28. When the generic name is not written in a prescription, this is a case of:

A. Violative prescriptionB. Erroneous prescription

C. Impossible prescriptionD. NOTA

Violative prescription:

•Generic name is NOT written•Generic name is NOT legible and brand name is legible•Brand name is INDICATED and instructions added (e.g. “NO SUBSTITUTION”)

Page 30: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

29. “Rule of Thumb” is the principle applied for testing:

A. AmpulesB. Implantations

C. VialsD. Compressed Tablets

Page 31: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

30. It refers to the release or movement of the components of the plastic container into the contents:

A. SorptionB. Absorption

C. AdsorptionD. Leaching

Sorption and Absorption – refers to the binding of drug molecules to the polymer material of the plastic container

Page 32: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

31. It states that vapor pressure of component is equal to its mole fraction times vapor pressure in the pure state at that same temperature.

A. Raoult’s lawB. Henry’s law

C. Charles’ lawD. Fick’s law

Page 33: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

32. Which of the following is not a colligative property?

A. Boiling point elevationB. Freezing point depressionC. Vapor pressure elevationD. Osmotic pressure

- vapor pressure LOWERING

Page 34: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

33. Dissociation constant for substances that dissociates into 5 ions

A. 4.2B. 1.8

C. 3.4D. 2.6

B – 2 ionsC – 4 ionsD – 3 ions

Page 35: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

34. Compute for the E value of Papaverine sulfate HCl (MW 376) which is a 2 ion electrolyte dissociating 80% in a given concentration.

A. 0.1554B. 0.1555

C. 0.1556D. 0.1557

E= (MW NaCl/i NaCl) x (i substance/ MW substance)E= (58.5/1.8) x (1.8/376)E= 0.15558 /0.1556

Page 36: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

35. A simplication of the White-Vincent method where the weight of the drug is fixed in 0.3g for one fluidounce of a 1% solution.

A. Modified White-Vincent methodB. Scowle’s methodC. Sprowl’s methodD. Cryoscopic method

Page 37: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

36. Dosage form made by compression or molding

A. TabletsB. Capsule

C. SyrupD. Suspension

Page 38: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

37. A characteristic of material for compression which describes the way the material flow thru the hopper

A. FluidityB. Compressibility

C. DrynessD. Particle size

Page 39: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

38. Spray drug lactose when used in direct compression can hold how many % of active ingredient?

A. 18%B. 15%

C. 20%D. 30%

It can hold 20-25% of the active ingredient

Page 40: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

39. Which of the following is not a glidant?

A. CAB-O-SILB. DL-Leucine

C. SyloidD. Talc

- It is solely used as an anti-adherent. (A), (C), & (D) are used as both glidant and anti-adherent. Glidants - improve flow property. Anti-adherent - prevents sticking & picking.

Page 41: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

40. Clays are limitedly used for what type of tablets due to its tendency to cause unwanted appearance?

A. White tabletsB. Colored tablets

C. BothD. NOTA

Page 42: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

41. Which solution is used as an astringent?

A. Strong iodine solution USPB. Aluminum acetate topical solution USPC. Acetic acid NFD. Aromatic ammonia spirit USPE. Benzalkonium chloride solution NF

Aluminum acetate - used as antiperspirants and wet dressings for contact dermatitisStrong iodine and Benzalkonium chloride – topical antibacterial solutionsAcetic acid - acidifierAromatic ammonia spirit – respiratory stimulant

Page 43: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

42. The particle size of the dispersed solid in a suspension is usually greater than

A. 0.5 μmB. 0.4 μmC. 0.3 μm

D. 0.2 μmE. 0.1 μm

A suspension is a two-phase system that consists of a finely powdered solid dispersed in a liquid vehicle

Page 44: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

43. In the extemporaneous preparation of a suspension, levigation is used to:

A. reduce the zeta potentialB. avoid bacterial growthC. reduce particle sizeD. enhance viscosityE. reduce viscosity

Levigation is the process of blending and grinding a substance to separate the particles, reduce their size, and form a paste.

Page 45: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

44. Which compound is a natural emulsifying agent?

A. acaciaB. lactoseC. polysorbate 20

D. polysorbate 80E. sorbitan

monopalmitate

Page 46: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

45. Rectal suppositories intended for adult use usually weigh approximately

A. 1 gB. 2 gC. 3 g

D. 4 gE. 5 g

Page 47: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

46. In the fusion method of making cocoa butter suppositories, which substance is most likely to be used to lubricate the mold?

A. Mineral oilB. Propylene glycolC. Cetyl alcohol

D. Stearic acidE. Magnesium silicate

Page 48: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

47. A very fine powdered chemical is defined as one that

A. completely passes through a #80 sieve.B. completely passes through a #120 sieve.C. completely passes through a #20 sieve.D. passes through a #60 sieve and not more than

40% through a #100 sieve.E. passes through a #40 sieve and not more than

60% through a #60 sieve.

Page 49: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

48. Which technique is typically used to mill camphor?

A. triturationB. levigationC. pulverization by

intervention

D. geometric dilutionE. attrition

Pulverization by intervention is the milling technique that is used for drug substances that are gummy and tend to re-agglomerate or resist grinding (e.g. camphor , iodine)

Page 50: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

49. The dispensing pharmacist usually blends potent powders with a large amount of diluent by

A. spatulationB. siftingC. trituration

D. geometric dilutionE. levigation

Page 51: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

50. Which type of paper best protects a divided hygroscopic powder?

A. waxed paperB. glassineC. white bond

D. blue bondE. vegetable parchment

Hygroscopic and volatile drugs are best protected by waxed paper , which is waterproof.

Page 52: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

51. This process is a form of pelletization, which refers to the formation of spherical particles from wet granulation

A. SpheronizationB. SluggingC. Spray chilling

D. Moist heatingE. Dry heating

•Slugging - a process in which the powder mixture is compressed into large flat tablet or pellet.

Page 53: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

52. Which excipient/s is/are used in the preparation of sugar-free chewable tablets?

I. Lactose II. Dextrose III. Xylitol

A. I onlyB. III onlyC. I and IID. II and IIIE. I, II, III

Page 54: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

53. This problem corresponds to the filling-in of the score line or indented logo on the tablet by the film.

A. PeelingB. PickingC. Orange peel effect

D. Mottling E. Bridging

•Peeling - appearance of large amounts of film fragments flaking from the tablet.

Picking – appearance of small amounts of film fragments flaking from the tablet.

Orange Peel Effect- pertains to the roughness of the tablet surface due to failure of spray droplets to coalesce.

Mottling- uneven distribution of color on the tablet surfaceBridging- Filling in of the score line or indented logo on the tablet by the

film.

Page 55: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

54. This type of dosage form allows a reduction in dosing frequency to that presented by a conventional dosage form

A. Extended releaseB. Delayed releaseC. Repeat Action

D. Modified ReleaseE. Targeted Release

Delayed release- designed to release the drug from the dosage form at a time other than promptly after administration.Repeat Action- Usually contains 2 doses of medication one for immediate and the second for delayed release.Targeted release - describes drug release directed towards isolating or concentrating a drug in a body region, tissue or site for absorption or for drug action.

Page 56: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

55. Yellow ointment is an example of

A. Hydrocarbon baseB. Oleaginous baseC. Absorption base

D. Water removable base

E. A & B

Hydrocarbon base is Oleaginous base

Page 57: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

56. The following ointment base/s is/are classified as hydrocarbon base/s

I. PetrolatumII. White ointmentIII. Polyethylene Glycol Ointment

A. I onlyB. I & IIC. I & IIID. III onlyE. I, II, III

Page 58: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

57. Polyethylene glycol Ointment, NF is:

A. Hydrocarbon baseB. Water Soluble baseC. Absorption base

D. Water Removable baseE. Oleaginous base

Page 59: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

58. These ointment base resembles cream in appearance

A. Hydrocarbon baseB. Water Soluble baseC. Absorption base

D. Water Removable base

E. Oleaginous base

Water removable bases are oil-in-water emulsion resembling creams in appearance. They are easily washed from skin and often called “water washable” base.

Page 60: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

59. These are semi-solid adhesive masses spread upon a backing material paper, fabric, moleskin or plastic

A. CreamB. PlasterC. Paste

D. OintmentE. Lotion

Page 61: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

60. The factor/s which play/s a part in percutaneous absorption is/are:

I. Molecular WeightII. Partitioning coefficientIII. Solubility

A. I onlyB. II onlyC. I & IID. II & IIIE. I, II, III

Page 62: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

61. In sugar coating of tablets, the greatest increase in the size of the tablet occurs at what stage of the process?

A. SealingB. SmoothingC. Color coating

D. Sub coatingE. Polishing

Page 63: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

62. Uneven distribution of color on the surface of tablets is:

A. PeelingB. MottlingC. Capping

D. LaminationE. Picking

Page 64: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

63. Strength of a product is expressed in terms of:

A. PotencyB. ActivityC. Toxicity

D. Therapeutic doseE. Lethal dose

Page 65: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

64. An example of a tetragonal crystal system is:

A. UreaB. Iodoform

C. IodineD. Sodium chloride

Iodoform – hexagonalIodine – rhombic

Sodium chloride - cubic

Page 66: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

65. These are properties which are dependent on the arrangement and to a lesser extent on the number and kind of atoms within a molecule:

A. IntensiveB. Colligative

C. ConstitutiveD. Extensive

Extensive – DEPENDENT on the quantity of matter in a systemIntensive – INDEPENDENT of the quantity of substance in the system (e.g. temperature, density, pressure, surface tension, viscosity)Colligative - e.g. Osmotic pressure elevation, vapor pressure lowering, Freezing point depression, and boiling point elevation

Page 67: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

66. These are solvents which are capable of acting both as proton acceptor and proton donor:

A. ProtophilicB. Protogenic

C. AmphiproticD. Aprotic

•Protophilic – solvents which are capable of accepting protons from the solute•Protogenic – solvent characterized to be proton-donating compound•Aprotic – solvents that neither accepts nor donate proton

Page 68: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

67. If a substance dissolves in a hundred to a thousand parts of solvent such substance is characterized to be:

A. SolubleB. Sparingly soluble

C. Slightly solubleD. Very slightly soluble

SOLUBILITY

Soluble 10 – 30 parts

Sparingly soluble 30 - 100 parts

Slightly soluble 100 – 1000 parts

Very slightly soluble 1000 – 10000 parts

Page 69: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

68. This is also known as the “shear thinning systems”

A. PseudoplasticB. Dilatant

C. ThixotrophicD. Rheopectic

Dilatant – “shear thickening system”Thixotrophic – gels and magmas when standing form semisolids and on shaking become fluid

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69. A phenomenon where in a gel takes up liquid without an observable increase in volume:

A. SweatingB. Syneresis

C. SwellingD. Imbibition

Syneresis – phenomenon in which the liquid portion of a gel is pressed outSwelling – process which involves the taking up of liquid by a gel with an observable increase in its volume

Page 71: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

70. This type of solution has a solute concentration equivalent to its limit of solubility

A. UnsaturatedB. Saturated

C. SupersaturatedD. NOTA

Page 72: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

71. Breaking down of materials by rubbing action between 2 surfaces.

A. AttritionB. Rolling

C. ImpactD. Scratching

Rolling - uses heavy rolling to crush materials. Impact - employs hammer/bars at high speed to break material.

Page 73: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

72. All are type of plastic containers, EXCEPT;

A. PVCB. PET

C. PPD. PD

PVC - polyvinyl chloridePET – polyethylenePP - polypropylene

Page 74: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

73. At what percent is is benzalkonium chloride used?

A. 0.2%B. 0.1%

C. 0.001%D. 0.002%

Page 75: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

74. A cool place would be

A. <8CB. 2-8C C. 8-15C

D. -20 - -15C

Page 76: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

75. Composition of the council of pharmaceutical education, EXCEPT;

A. Secretary of EducationB. Dean of UP College of PharmacyC. BFADD. DOST Secretary

Page 77: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

76. Qualification for Board examination, except;

A. Citizen of the PhilippinesB. Moral characterC. Completed internshipD. BS Pharmacy graduateE. NOTA

Page 78: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

77. Revocation of LTO may be due to the following except;

A. Selling of drug with “not for sale” markB. Failure to properly record dangerous drugsC. Absence of pharmacistD. AOTAE. NOTA

Page 79: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

78. RA 7432

A. Senior Citizen’s ActB. Pharmacy Law

C. Generic’s ActD. Dangerous Drugs Act

Page 80: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

79. RA 6425

A. Senior Citizen’s ActB. Pharmacy Law

C. Generic’s ActD. Dangerous Drugs Act

Page 81: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

80. RA 6675

A. Senior Citizen’s ActB. Pharmacy Law

C. Generic’s ActD. Dangerous Drugs Act

Page 82: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

81. A certain drug is considered counterfeit if it contains less than how many percent of the active ingredient it purports to posses?

A. 80B. 75C. 60

D. 85E. 90

Counterfeit drug/medicine refers to a drug which contains no amount of, or different active ingredients or less than eighty percent of the active ingredient it purports to possess (RA 8203, Section3)

Page 83: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

82. For how many years shall the Chairman and members of the Board of Pharmacy hold office after appointment?

A. 3B. 4C. 5

D. 6E. 2

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83. Any person who shall be employed as detailman by any pharmaceutical establishment shall be required to register with the:

A. PRCB. BFADC. Board of PharmacyD. DOHE. Council of Pharmaceutical Education

Page 85: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

84. Every prescription for external use filled in the drugstore shall bear what label?

A. Red labelB. White labelC. Red label showing in blank ink the components

and the word “External Use Only”D. White label showing red ink the Word “External

Use Only”E. NOTA

Page 86: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

85. The pharmacist examination shall consist of the theoretical examination on the subjects in:

A. ChemistryB. Biological ScienceC. Pharmacy

D. A and C OnlyE. AOTA

Page 87: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

86. The book kept for the purpose of recording the sale of poisons shall be open at all timed for inspection and shall be preserved for a period of at least __________ years after the last entry.

A. 1B. 2C. 3

D. 5E. 7

Page 88: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

87. The following substances are included in the list of violent poisons stated in RA 5921:

A. AtropineB. NitrobenzeneC. Strychnine

D. B and C onlyE. AOTA

Also include in the list are arsenical preparations, phosphorus, corrosive sublimate, hydrocyanic acid or prussic acid and such other poisonous substances which may be classified as violent by BFAD (RA 5921, Article IV, Section 34)

Page 89: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

88. This means a system of words or other systems arbitrary used to present words.

A. CodeB. CipherC. Secret Keys

D. SubstitutionE. NOTA

Page 90: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

89. The term Secretary, in RA 3720, means:

A. Secretary of DOHB. Secretary of Dept of Commerce and IndustryC. Secretary of EducationD. Secretary of Department of Agricultural

ResourcesE. AOTA

Page 91: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

90. Under RA 3720, if a food bears or contains any poisonous or deleterious substances which may render it injurious to health, it is deemed to be:

A. PoisonB. AdulteratedC. Misbranded

D. CounterfeitE. Hazardous

Page 92: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

91. If the seized drug was found to be counterfeit, the business establishment must be directed for preventive closure for a period of:

A. 15 daysB. 10 daysC. 30 days

D. 20 daysE. 60 days

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92. If the counterfeit drug is the proximate cause of death of the victim who unknowingly purchased and took the counterfeit drug, the penalty to be imposed shall be:

A. Life imprisonmentB. Fine of 500,000 to 5M PesosC. Fine of 100,000 to 10M PesosD. A & B OnlyE. A & C only

Page 94: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

93. The council of Pharmaceutical Education was created for the implementation of RA 5921. This council is composed of:

A. Secretary of Education B. BFAD administrator C. Chairman of the Board of PharmacyD. A & CE. AOTA

Other members are Undersecretary of Health Service, Dean of UP College of Pharmacy, Deans of the Colleges of Pharmacy representing duly, accredited private schools of pharmacy and a representative of a bona fide national pharmaceutical organization of the Philippines.

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94. If found guilty of neglect of duty, incompetence, malpractice or unprofessional or dishonorable conduct, after having been given the opportunity to defend himself in an administrative investigation, the Chairman or members of the Board may be removed by:

A. President of the PhilippinesB. Chairman of the Council of Pharmaceutical

EducationC. BFAD administratorD. PRC ComissionerE. Civil Service Commissioner

Page 96: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

95. Any person who shall be employed as detailman by any pharmaceutical establishment shall be required to register with the

A. PRCB. BFADC. Board of PharmacyD. DOHE. Council of Pharmaceutical Education

Page 97: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

96. Every prescription for external use filled in the drugstore shall bear what label

A. Red labelB. White labelC. Red label showing in black ink the component

and the words “For external use only”D. White label showing in red ink the word “For

external use only”E. NOTA

Page 98: MODULE 5 Pharmaceutics. 1. RA 8203 was signed into law on: A.September 4, 1996 B.September 13, 1988 C.October 4, 1996 D.September 13, 1986 E.September.

97. The book kept for the purpose of recording the sale of poisons shall be open at all times for the inspection and shall be preserved for a period of at least ____ years after the last entry

A. 1B. 2C. 3

D. 5E. 7

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98. RA 3720 was signed into law on:

A. June 22, 1963B. June 22, 1969C. June 23, 1969

D. July 22, 1969E. July 22, 1963

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99. Prescription of Dangerous Drugs are written in:

A. DuplicateB. Triplicate C. One copy

D. Four copiesE. NOTA

one original, 2 duplicates ( Original- pharmacist, 1 copy- patient, 1 copy- practitioner)

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100. Head of the PDEA

A. Secretary of HealthB. Director GeneralC. NBI Chief

D. PNP ChiefE. BFAD Director