Jurisprudence Flashcards
- Science of philosophy of laws
- A system of laws
JURISPRUDENCE
Define and regulate Pharmacy Profession and delimit
its practice
PHARMACY LAWS
- Science of morality
- Moral principle of practice
ETHICS
LEGAL and ETHICAL control governing PHARMACY PROFESSION
PHARMACEUTICAL JURISPRUDENCE AND ETHICS
RA5921
PHARMACY LAW
JUNE 23, 1969
RA10918
THE PHILIPPINE PHARMACY ACT
JULY 21, 2016
SPECIAL LAW ON COUNTERFEIT
DRUGS
SEPT 4, 1996
RA 8203
RA3720
FOOD DRUG DEVICES AND COSMETICS ACT
JUNE 22, 1963
PRICE ACT
RA 7581
MAY 27, 1992
FOOD AND DRUG ADMINISTRATION
ACT OF 2009
RA 9711
AUG 18, 2009
CONSUMERS ACT OF THE PHILIPPINES
RA 7394
APRIL 13, 1992
RA 6425
MARCH 30, 1972
DANGEROUS DRUG ACT OF 1972
SENIOR CITIZENS ACT
APRIL 23, 1992
RA 7432
RA 9165
JANUARY 23, 2002
COMPREHENSIVE DANGEROUS DRUG ACT 2002
EXPANDED SENIOR CITIZENS
ACT OF 2003
FEBRUARY 26, 2004
RA 9257
RA 9994
EXPANDED SENIOR CITIZENS
ACT OF 2010
FEBRUARY 15, 2010
GOVERNMENT PROCUREMENT
REFORM ACT
JANUARY 10, 2003
RA 9184
UNIVERSALLY ACCESSIBLE
CHEAPER AND QUALITY MEDICINES ACT 2008
RA 9502
JUNE 6, 2008
TOBACCO REGULATION ACT OF 2003
RA 9211
JUNE 23, 2003
RA 6675
SEPTEMBER 13,1988
GENERICS ACT OF 1988
RA 10354
RESPONSIBLE PARENTHOOD AND REPRODUCTIVE HEALTH BILL
DECEMBER 21, 2012
CONTINUING PROFESSIONAL
DEVELOPMENT OF 2016
RA 10912
JULY 21, 2016
RA 8432
TAMA
DECEMBER 9,1997
PRC MODERNIZATION ACT
DECEMBER 5, 2000
RA 8981
MILK CODE OF THE PHILIPPINES
Eo 51
OCTOBER 28, 1986
Initial Period (Initial Application)
1 year
ASIN LAW, SALT W/IODINE
DECEMBER 20, 1995
RA 8172
“ An act to ensure the safety and purity of foods and cosmetics, and the purity, safety, eficacy and quality of drugs and devices being made available to the public, vesting the BFAD with authority to administer and enforce the laws pertaining thereto, and for other purposes.”
FOODS, DRUGS, DEVICES & COSMETICS ACT
FOOD SAFETY ACT OF 2013
AUGUST 23, 2013
RA 10611
instrument, apparatus, or contrivances, including their components, parts, and accessories, intended:
- for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in man or animals
“DEVICE”
- 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 the appearance
- articles intended for use as a component of any such articles
“COSMETICS”
- articles used for food or drinks for man
- chewing gum
- articles used for components of such article
“ FOOD”
IMPLEMENTING AGENCY
- COUNCIL OF PHARMACEUTICAL EDUCATION
- BOARD OF PHARMACY
may render it injurious to health
Adulterated Food
- Articles recognized in the current oficial USP-NF, oficial Homeopathic Drug Formulary, or any supplement to any of them
- Articles intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in man or other animal
- Articles (other than food) intended to affect the structure or any function of the body of man of animals
“DRUG”
If its labeling is false or misleading
Misbranded Food
“An act to maximize the contribution of senior citizens to nation building, grant benefits, and special privileges and for other purposes”
SENIOR CITIZENS ACT
An act granting additional benefits and privileges to senior citizens amending for the purpose R.A. 7432
EXPANDED SENIOR CITIZENS ACT OF 2003
Subsequent Period (Renewal Application)
2 years
If it is offered for sale under the name of another food
Misbranded Food
any resident citizen of the Philippines at least 60 years old
SENIOR CITIZEN or ELDERLY
GROUNDS FOR NON – RENEWAL OF LTO
- Failure to comply or rampant violation of existing
laws, rules and regulations - Failure to assures the safety, eficacy & quality of its
drug products
If it purports to be or is presented for special dietary uses
Misleading
“An act prohibiting counterfeit drugs, providing penalties for violations and appropriating funds therefore”
Special Law on Counterfeit Drugs
engaged in operations
Drug manufacturer
If it is an imitation of another food
Misbranded Food
4S
- Segregate
- Seal
- Search warrant
- Seize
“ An act providing protection to consumers by stabilizing the prices of basic necessities and prime commodities and by prescribing measures against undue price increase during emergency situations and like occasions”
R.A. 7581
- DD/ Importer
- DD/Exporter
- DD/Wholesaler
Drug Distributor
Undue accumulation of any basic or prime commodities beyond its normal inventory level or refusal to dispose or sell stocks to the general public.
HOARDING
The generic name is not written
VIOLATIVE Rx
Selling of basic and prime commodity at a price in excess of its worth.
PROFITEERING
It is the policy of the state to protect the interest of the consumer, promote his general welfare and to establish standards of conduct for business and industry.
Approved: April 13, 1992
CONSUMER ACT OF THE PHILIPPINES
- registered owner of the drug product
- procures the raw materials & packing components
- engage in distribution & / or marketing
- sub-contractor
Drug trader
Agreement between 2 or more persons to unreasonably increase or manipulate its price
CARTEL
any person whether related to the senior citizens or not who takes care of him/her as a dependent
BENEFACTOR
What are the requirements to purchase the medicine and avail the 20% discount?
Present the National Identification Card and
his purchase slip booklet duly approved by
the OSCA chairman
Only the generic name is written but is not legible
IMPOSSIBLE Rx
is a simpler term for the scientifically recognized active ingredient of a drug
GENERIC NAME
means dispensing the patients’/ buyers’ choice among the generic equivalents, i.e. finished pharmaceutical products having the
same active ingredient(s) same
dosage form and same strength as the prescribed drug.
GENERIC DISPENSING
list of drugs that meet the health care needs of the majority of the population
CORE LIST
list of alternative drugs used when there is no response to the core essential drug, when there is hypersensitivity reaction or if it cannot be given
COMPLEMENTARY LIST
The generic name is the one in the parenthesis
ERRONEOUS Rx
The brand name is not in the parenthesis
ERRONEOUS Rx
Both generic name and the brand name are not legible
IMPOSSIBLE Rx
means dispensing less than the total number of units prescribed.
PARTIAL FILLING OF PRESCRIPTION
branch of medical science devoted to the study of the biological and physical changes and the diseases of old age
GERIATRICS
“An act to promote, require, and ensure the production of an adequate supply, distribution, use, and acceptance of drugs
and medicines identified by their generic name”
GENERICS ACT OF 1988
any person so defined in the National Internal Revenue Code,
as amended
HEAD of the FAMILY
- Shall not be filled
- Shall be kept & reported by the pharmacist to the nearest DOH office
- Pharmacist shall advise the prescriber of the problem
- Instruct the customer to get proper Rx
VIOLATIVE AND IMPOSSIBLE Rx
proprietary name given by the manufacturer to distinguish its production from those of competitors
BRAND NAME
The brand name precedes the generic name
ERRONEOUS Rx
An act instituting the Comprehensive Dangerous Drugs Act of 2002, repealing Republic Act No. 6425, otherwise known as the Dangerous Drugs Act of 1972, as amended, providing funds therefore, and for other purposes
R.A. 9165
PENALTY:
DANGEROUS DRUGS
Life imprisonment to death & a fine ranging from Php
500,000 to Php 10M
act by validly registered Pharmacist of filling a prescription or doctor’s order on the patient’s chart.
DISPENSING
The generic name is not legible and a brand that is legible is written
VIOLATIVE Rx
The brand name is indicated and instructions (such as the phrase “NO SUBSTITUTION”)
VIOLATIVE Rx
The generic name does not correspond to the brand name
IMPOSSIBLE Rx
- Shall be filled
- Shall be kept & reported to the nearest DOH office
ERRONEOUS Rx
PENALTY:
CONTROLLED PRECURSORS AND ESSENTIAL CHEMICALS
Imprisonment ranging from 12 years & 1 day to 20
years and a fine of Php 100,000
S LICENSES REQUIRED
for persons dealing in exempt Dangerous Drugs Preparation
S-1
S LICENSES REQUIRED
for compounders, producers and
manufacturers
S-5-C
S LICENSES REQUIRED
for physicians, dentist, and veterinarians, lawfully entitled to distribute, dispense or administer
any dangerous drugs.
S-2
S LICENSES REQUIRED
for retail dealers
S-3
S LICENSES REQUIRED
for wholesale dealers
S-4
S LICENSES REQUIRED
for importers of raw materials & finished products
S-5-1
S LICENSES REQUIRED
for persons not registered as importer, manufacturer, producer or compounders but lawfully entitled to obtain and use in a laboratory dangerous drugs for the purpose of research, instruction or analysis.
S-6
S LICENSES REQUIRED
for importer, manufacturer, producers or compounder of dangerous drugs in any form, their
salts, isomers, any material, compound, mixture or preparation which contains any quantity of dangerous drugs, and exempt preparation imported into or
produced in the Philippines
S-7
drug approved or sale to the general public without restriction other than usual
DRUG FOR GENERAL USE
FOOD AND DRUG ADMINISTRATION ACT OF 2009
R.A. 9711
An act providing for cheaper and quality medicines amending for the purpose republic act no 8293 or the intellectual property code, R.A. No. 6675 or the generics act of 1988 and republic act 5921 or pharmacy law.
R.A. 9502
An act creating the Philippine Institute of Traditional and Alternative Health Care (PITAHC) to accelerate the development of traditional and alternative health care in the Philippines, providing for a traditional and alternative health care development fund and for other purposes.
THE TRADITIONAL AND MEDICINE ACT OF 1997 (TAMA)
drug approved for sale to
the general public under certain conditions
DRUG FOR RESTRICTED USE
means the process of approval for the manufacture, importation, exportation, sale, offer for sale, distribution or transfer of pharmaceutical products containing active ingredient(s) of known chemical structure & properties to be safe, eficacious, and of good quality according to standards of BFAD
REGISTRATION
“ PRC Modernization Act of 2000”
R.A. No. 8981
RA 5921 was signed into law on
A. June 23, 1969
B. June 23, 1963
C. June 22, 1969
D. June 22, 1963
June 23, 1969
RA 5921 provides for and shall govern:
A. Standard’n & regulation of pharm education
B. Examination for registration of graduates of school of
pharmacy
C. Supervision, control & regulation of the practice of
pharmacy in the Phil.
D. A and C only
E. AOTA
E. AOTA
For the purpose of implementing RA 592 these were created:
A. Board of Pharmacy
B. Council of Pharm’l Educ.
C. PRC
D. A & B only
E. AOTA
D. A & B only
For how many years shall the chairman & members of the
board hold ofice?
A. 3
B. 4
C. 5
D. 6
A. 3
. To be appointed member of the Board has been in the
practice of Pharmacy for
A.5
B.7
C. 8
D. 10
D. 10
This is a requirement for the opening of d/s
A. Filipino registered pharmacist
B. 7x5 drugstore space
C. Drugstore label
D. Record books
A. Filipino registered pharmacist
Any of the f shall be a ground for reprimanding, suspending
or revoking the cert. of registration.
A. Immoral or dishonorable conduct
B. Fraud or deceit in the acquisition of cert.
C. Insanity
D. A & B only
E. AOTA
E. AOTA
Which Exec. Order abolished the Food & Drug Adm. and
created the BFAD?
A. EO 137
B. EO 851
C. EO 951
D. EO 147
B. EO 851
The division of BFAD which is in charge in the inspection and
licensing of the manufacturer of food, drug and cosmetics:
A. Regulation Division I
B. Legal Division
C. Product Service Div
D. Regulation Division II
D. Regulation Division II
This s a proof that a person is a licensed pharmacist:
A. Transcript of record
B. Diploma
C. Cert. of registration
D. Certificate of internship
Cert. of registration
To encourage the development of a botanical garden is one
function of:
A. Board of Pharmacy
B. BFAD
A. Board of Pharmacy
Age requirement in order to practice pharmacy
A. 18
B. 25
C. 21
D. 20
C. 21
Method of secret writing w/c substitutes other letters or
transposes the letter after arranging them in blocks
A. Cipher
B. Code
C. Secret keys
D. Any of the above
A. Cipher
Record for the sale of poisons must be kept for:
A. 5 years
B. 1 year
C. 3 years
D. 2 years
A. 5 years
RA 3720 was signed into law on:
A. June 22, 1963
B. June 22, 1969
C. June 23, 1969
D. July 22, 1969
A. June 22, 1963
A food shall be deemed to be adulterated if:
A. Prepared, packed, held under unsanitary condition
B. Damage or inferiority, concealed in any manner
C. Ofered for sale under the name of another food
D. A & B only
E. AOTA
D. A & B only
If the food is an imitation of another food:
A. Fake
B. Misbranded
C. Misleading
D. Adulterated
B. Misbranded
Among the prohibited act under RA 3720 are:
A. Manufacture for sale, distribute declared as banned
B. Adulteration or misbranding of any food, drug
C. Manufacture, sale, distribution of any drug not registered
with BFAD
D. B and C only
E. AOTA
D. B and C only
Shall provide for the certificate of batches of drugs
composed wholly or partially any kind of antibiotics
A. Secretary of Health
B. PRC Commissioner
C. BFAD Director
D. BFAD Administrator
A. Secretary of Health
Drugs are considered adulterated if:
A. Label is misleading
B. An imitation of a product
C. Differs from USP Std.
D. NOTA
C. Differs from USP Std.
RA 3720 was amended by EO:
A. 881
B. 851
C. 175
D. 170
C. 175
Any person who commits the following shall be penalize for
6mon-5 yrs imprisonment & fine >1000
A. Sale of any drug beyond its expiration date
B. Distribution of batches of drugs w/o batch cert.
C. Forging, counterfeiting w/o proper authority
D. A & C only
E. AOTA
E. AOTA
The Division of BFAD that certifies batches of antibiotics:
A. Product Services
B. Laboratory Services
C. Legal Info & Compliance
D. Inspection Services
B. Laboratory Services
A prevailing price be placed under automatic price control
except:
A. State of calamity
B. Declared under an emergency
C. Declare in a State of rebellion
D. Privilege of the writ
E. NOTA of habeas Corpus
A. State of calamity
D. Privilege of the writ
In order to manufacture, sell, distribute any drug, a license
to operate shld. be first secure from:
A. BFAD
B. DTI
C. PRC
D. Dept of Commerce
A. BFAD
Appoints the Sectoral representative of the Price
Coordinating Council:
A. Secretary of Trade & Industry
B. President of the Philippines
C. Secretary of DA
D. Secretary of DENR
B. President of the Philippines
Directing measures to prevent hoarding, profiteering and
price manipulation:
A. Letter of Instruction 1305
B. Letter of Instruction 1342
C. Letter of Instruction 1359
D. Letter of Instruction1349
C. Letter of Instruction 1359
Penalty for acts of illegal price manipulation is:
A. Imprisonment for 1 year and NMT 10 years.
B. Fine for NLT Php 5,000 and NMT 1 million.
C. Imprisonment for NLT 5 years and NMT 15 years.
D. Fine of NLT Php 500,000 and NMT 2 million.
C. Imprisonment for NLT 5 years and NMT 15 years.
FF conditions may impose a price ceiling except:
A. Existence of calamity
B. Existence of an emergency
C. Widespread illegal price Manipulation
D. NOTA
D. NOTA
- Factors in determining reasonable price ceiling:
A. Supply available in the market
B. Peso exchange rate
C. Change in the amortization cost
D. AOTA
D. AOTA
RA 7431 was signed into law on:
A. April 23, 1992
C. February 13, 1992
B. February 7, 1992
D. April 13, 1992
A. April 23, 1992
The government agency w/c issues National ID card and
purchase slip booklet:
A. DSWD
B. GSIS
C. OSCA
D. BFAD
C. OSCA
Any person maybe a relative or not who takes care of senior
citizen as dependent:
A. Head of the family
B. Relative
C. Benefactor
D. Care giver
C. Benefactor
The Expanded Senior Citizens Act of 2003 is also known as:
A. RA 9265
B. RA 9165
C. RA 9275
D. RA 9257
D. RA 9257
The discount privileges of the senior citizen shall be:
A. Non transferable
B. Transferable but limited for senior citizen
C. Limited and exclusive for senior citizen
D. Both A and C
D. Both A and C
The term “senior citizen” shall mean any resident citizen at
least ___ years old:
A. 50
B. 55
C. 60
D. 65
C. 60
OSCA refers to:
A. Office of Senior Citizen Affiliate
B. Office of Senior Citizen Affairs
C. Office of Senior Citizen’s Academy
D. NOTA
B. Office of Senior Citizen Affairs
Supplies of medicine to be given shld not exceed:
A. One day supply
B. One week supply
C. One month supply
D. One year supply
C. One month supply
RA 6675 was signed into law on:
A. Sept. 23,1998
B. Sept. 13, 1988
C. Sept. 4, 1988
D. Sept. 30, 1988
B. Sept. 13, 1988
Violation of any provision of senior citizen act is
punishable by:
A. Fine not exceeding 2,000 pesos
B. Imprisonment not exceeding 1mon & fine not exceeding
1,000 pesos
C. Imprisonment not exceeding 2 months
D. Both A and C
B. Imprisonment not exceeding 1mon & fine not exceeding
1,000 pesos
Which of the f shld be presented by senior citizen:
A. Purchase slip booklet
B. Prescription
C. Birth Certificate
D. National ID card
E. A, B & D
F. AOTA
E. A, B & D
Rules & regulations to implement dispensing requirement
under the Generics Act of 1988:
A. AO 63
B. AO 64
C. AO 65
D. AO 66
A. AO 63
Under the generics law, w/c of this Rx shall be filled.
A. Violative
B. Impossible
C. Erroneous
D. NOTA
C. Erroneous
If the brand name precedes the generic name, the Rx
A. Violative
B. Impossible
C. Erroneous
D. Coded
C. Erroneous
FF are the violations on the part of dispensers & outlet
A. Failure to record & keep Rx filled
B. Imposing a particular brand or product
C. Failure to report to the nearest DOH ofice
D. Both A and B
E. AOTA
E. AOTA
When the drug product prescribed is not registered w/ BFAD,
this is a case of:
A. Violative Rx
B. Impossible Rx
C. Erroneous Rx
D. Coded Rx
B. Impossible Rx
Generic prescribing is also known as:
A. AO 61
B. AO 62
C. AO 63
D. AO 64
B. AO 62
What is to be done with violative prescription:
A. Shall be filled & kept
B. Not be filled & report to nearest DOH
C. Shall be mark w/ red ink
D. torn
B. Not be filled & report to nearest DOH
Which if the f is an erroneous Rx.
A. Generic name is not legible & brand name is legible
B. Brand name is not in parenthesis
C. Only generic name is written but not legible
D. AOTA
Brand
name is not in parenthesis
Corelistmeans:
A. List of drugs that meet health care needs
B. List of drugs that meet the requirements established
by Pharmaceutical Assn
C. List of drugs with corresponding brand names.
D. AOTA
List of drugs that meet health care needs
