Answer the questions and click the"Finish Exam" button.

1. Medicines that do not require a prescription and may be

sold in non-pharmacy outlets:* 2.

Medicines Fraction V
Medicines Fraction I
Medicines Fraction VI
Medicines Fraction III
2. The elements to be contained in the refrigerator/freezer
record for the preservation of medicines are the
establishment data, folio and instrument data, temperature
range outside the specifications of the standard,
temperature range within the specifications of the
standard, and...*.

Signature of the person in charge of health care

Date and time
Bar code authorized by the Ministry of Health
Area where the temperature is recorded
3. The following are some of the elements that should be
included in the antibiotic registry in your control books:* 1.

Progressive internal number assigned to each retained prescription, complete

presentation, name of the laboratory responsible for the antibiotic.
Date of entry and exit, distinctive and/or generic name, complete presentation, name,
address and professional license number of the physician prescribing the antibiotic.
Distinctive and/or generic name, batch number and expiration date of the antibiotic
Prescribing physician's name and professional license number, patient's name, sanitary
registration of the laboratory
4. In the sanitary registers of medical devices, what code
did COFEPRIS assign to prostheses, orthoses, surgical and
healing material, dental supplies and hygienic products?
 C
H
E
R
5. Mexican Official Standard that establishes the guidelines
for the installation and operation of Pharmacovigilance:* 6.

NOM-220-SSA1-
2012
NOM-262-SSA1-
2012
NOM-264-SSA1-
2012
NOM-240-SSA1-
2012
6. In case of a suspected Adverse Drug Reaction, what are
the steps to follow to report it?

I. Go to www.ram.gob.mx, II. Download the Adverse Drug Reaction Report Form. III.
Fill out your report and submit it to your primary care physician.
I. Enter the COFEPRIS website, II. Locate in the Carousel of sites of interest the option
Did any medication harm you, III. Display the online Suspected Adverse Drug Reaction
Reporting Format.
I. Ask your physician for the Adverse Drug Reaction Report Form, II. Fill out your
report with the drug data, III. Send your format to ram@farmacovigilancia.gob.mx
I. Ask your physician for the Adverse Drug Reaction Report Form, II. Fill out your
report with the drug data, III. Send your format to reaccionesadversas@ram.gob.mx
7. According to Article 226 of the General Health Law, the
drugs in Groups I, II and III are referred to as follows

Controlled drugs
Magistral medicines
Drugs for sale and supply
Specialty drugs
8. They are toxic substances that have lost, lack or present
variation in the characteristics to be used, transformed or
commercialized with respect to the original design or
production standards:*

Hazardous waste
Biodegradable waste
Organic waste
Toxic waste
9. Is the correct final disposition for expired medicines:*.

A waste management plan authorized by the SEMARNAT

(SEMARNAT)
Destroy them and dispose of them down the drain.
Throw them away in a separate bag
Burning them in the open air
10. It is responsible for collecting, monitoring, investigating
and evaluating information on the effects of drugs,
biological products, medicinal plants and traditional
medicines, with the aim of identifying information on new
adverse reactions, knowing their frequency and preventing
harm to patients:*.

Adverse Event Reporting

Technovigilance
Health verification of
pharmaceuticals
Pharmacovigilance
11. These drugs should be stored in metal or solid wood
furniture, with a metal plate for their safekeeping and
custody, and should never be in self-service areas:*.

Controlled drugs
 OTC
Brand name drugs
Generic drugs
12. It is the maximum temperature variation range allowed
to preserve the properties of medicines and other health
supplies:*.

Between 4 °C and 10
°C
Between 2 °C and 8
°C
Between 2 °C and 6
°C
Between 3 °C and 7
°C
13. You have the responsibility to ensure that there is no
recurrence of an adverse incident involving the use of a
medical device.

The holder of the sanitary registration of the medical device

The Federal Commission for the Protection against Sanitary Risks
(COFEPRIS)
The establishment that markets the medical devices
The National Center for Pharmacovigilance
14. It is a requirement that must be fulfilled for the
prescription of medicines:*.

The prescription shall be only by means of a computerized system to ensure that it is

legible.
Contain acronyms, codes, secret signs, abbreviations or chemical symbols to prevent
forgery
The prescription shall be in Spanish language, in written and/or computerized form.
Prescribes duly authorized health personnel or any person to whom the duly authorized
health personnel or any person to whom the duly authorized health personnel or any person
to whom the duly authorized health personnel delegates this function
15. It is the medical prescription issued by authorized
professionals for the prescription of Group I drugs:*.

Ordinary
Special
Authorized
Customized
16. Prescriptions for controlled medications can only be
filled when issued by:*

Physicians, medical specialists, homeopaths, dental surgeons and veterinary doctors

Physician and medical representative
Physicians and pharmacy health manager
Medical specialists
17. The following are some susceptibility factors for which
an adverse drug reaction may occur:*.

Previous adverse drug reactions and blood transfusions

Diet, concomitant treatments, blood type
Allergies, hereditary diseases, infections
Age, gender, concomitant pathologies, general allergy history
18. It is an Adverse Drug Reaction that should be reported:*

Reaction that causes nausea effects.

Reaction to newly introduced therapeutic drugs.
Reaction that causes drowsiness effects.
Reaction that causes vertigo effects.
19. The following drugs are included in the classification
according to their preparation, pursuant to Article 224 of
the General Health Law:*.

Homeopathics, Herbalists, Allopathics

 Sections I, II, III, IV, V and VI
Innovators or reference products
Pharmaceutical, Magistral and Oficinal Specialties
20. It is the set of methods and observations that allow us
to detect adverse incidents during the use of a medical
device, which may cause harm to the patient, operator or
the surrounding environment.

Pharmacovigilance
Technovigilance
Sanitary verification of medical devices
Adverse reaction to medical devices
21. Medicines prepared in accordance with the guidelines
of the Pharmacopoeia of the United Mexican States, the
Herbal Pharmacopoeia of the United Mexican States, the
Homeopathic Pharmacopoeia of the United Mexican States
and the Supplement for establishments dedicated to the
sale and supply of medicines and other health supplies
are:*.

Oficinal Medicines
Herbal Medicines
Allopathic Medications
Magistral Medicines
22. For the sale of these drugs, which is retained in the
pharmacy and recorded in the control books:* 22.

Medicines Fraction II
Medicines Fraction I
Medicines Fraction IV
Medicines Fraction III
23. This drug corresponds to fraction VI and may be
dispensed in other establishments that are not
pharmacies:*

Lithium
carbonate
Omeprazole
Triazolam
Amoxicillin
24. It is a system designed by the pharmaceutical industry
for the management and final disposal of drug waste and
its packaging in the hands of the public:*

SINGREM
SMDMC
SNFV
SEMARNAT
25. The meaning of the acronym PNO is:*.

Standardized and Operational Process

Regulatory and Operational Process
Standard Operating Procedure
Regulatory and Operating Procedures
26. It is an effect caused by expired drugs:*.

Destroys pathogenic microorganisms

It generates resistance to pathogenic
microorganisms.
Changes color, but retains its properties
Keeps a bad odor, but retains its properties
27. It is defined as the supply or delivery of one or more
drugs and medical devices to a patient and the respective
information on their proper use by a health professional:*
27.
 Distribution of medicines
Marketing of medicines
Sale of medicines
Dispensing of medicines
28. Products made from plant material or any derivative
thereof whose main ingredient is the aerial or subway part
of a plant or extracts and tinctures, as well as juices,
resins, fatty and essential oils, presented in
pharmaceutical form, whose efficacy and safety have been
scientifically confirmed:*.

Herbal Remedies
Naturopathic Medicines
Homeopathic Medicines
Herbal Medicines
29. The Hydrotalcite, is part of the drugs of the:*.

Group I
Group
IV
Group II
Group V
30. The following are aspects to be taken care of by the
personnel working in a pharmacy:*.

Maintain safe and hygienic conditions, identify the product required and verify its
existence.
Have a service attitude and always recommend the most economical drugs.
Prescribe the appropriate medication for the patient's condition, be respectful and
courteous.
Greet customers courteously and prepare quality injectable mixtures if requested by the
user
31. Is the correct order of the stages of assistance in the
dispensing of medicines in pharmacies:*.

I. Customer service, II. User reception, III. Drug group identification, IV. Know the
labeling information, V. Promote the rational use of medicines.
I. User reception, II. Identification of the drug group, III. Know the labeling
information, IV. Customer service, V. Promote the rational use of medicines.
I. User reception, II. Customer service, II. Identification of the group of drugs. IV.
Promote the rational use of medicines, V. Know the labeling information.
I. User reception, II. Customer service, III. Promote the rational use of medicines, IV.
Know the labeling information, V. Identification of the group of drugs.
32. Medical devices whose designation key in the sanitary
registries according to their category of use is the letter
"R":*.

Dental supplies and hygienic products

Surgical and healing material
Prosthetics, orthotics and functional aids
Diagnostic agent
33. Prescription drugs that can be filled up to a maximum
of three times

Medicines Fraction III

Medicines Fraction V
Medicines Fraction II
Medicines Fraction I
34. Medicines that can be acquired only with a special
prescription issued by the Ministry of Health:* 34.

Medicines Fraction VI
Medicines Fraction I
Medicines Fraction III
Medicines Fraction V
35. Pharmaceutical products, drugs or medicinal
specialties whose administration does not require medical
authorization, since they are used by consumers under
their own initiative and responsibility are as follows

Over-the-counter (OTC) drugs

Similar drugs
Expired medicines
Generic drugs
36. In the sanitary registries of medicines, which code was
assigned by the Health Secretariat to the Allopathic
medicines?

M
F
P
A
37. It is the set of guidelines that, under the direction of
the health authority, aims to guarantee universal access to
and responsible consumption of high quality medicines and
other health supplies for the benefit of the population:*.

Internal Regulations for establishments engaged in the sale and supply of medicines
Drug Dispensing Agreement
Regulations for the dispensing of medicines
Pharmaceutical policy
38. This is the year in which the Agreement determining
the guidelines to which the sale and dispensing of
antibiotics shall be subject was published.

2008
2011
 2009
2010
39. Pursuant to Article 226 of the Health Supplies
Regulations, for their sale and supply, medicines are
classified as follows

6 fractions or groups
4 fractions or groups
3 fractions or groups
8 fractions or groups
40. It is defined as the thermal degree or level of a body or
the atmosphere and is the indicator of the amount of heat
energy accumulated in the air:* 40.

Atmospheric
pressure
Temperature
Thermal sensation
Humidity