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Pharmacology of Quinolones

Total questions: 11

Worksheet time: 4mins

Name
Class
Date
1.

How different is the MOA of fluoroquinolones in G+ and G- microbes?

a)

In G+ve, more activity towards DNA gyrase

b)

In G-ve - more activity towards DNA gyrase

c)

In G+ve, more activity towards topoisomerase IV

d)

In G-ve, more activity towards topoisomerase IV

e)

No difference

2.

How many generations of quinolones that have been currently listed?

a)

Two (2)

b)

Three (3)

c)

Four (4)

d)

Five (5)

3.

Which of the following is NOT the mechanism of resistance to fluoroquinolones?

a)

Alterations in DNA gyrase

b)

Alterations in topoisomerase IV

c)

Increase influx of drugs

d)

Decrease uptake of drug

4.

The first drug under quinolone group is

a)

clavulanic acid

b)

fluoroacetic acid

c)

nalidixic acid

d)

naxidilic acid

5.

Which of the following is the primary excretion route for most fluoroquinolones?

a)

Renal

b)

Liver

c)

Skin

6.

Which of the following agent is not primarily excreted via renal?

a)

Ciprofloxacin

b)

Norfloxacin

c)

Levofloxacin

d)

Moxifloxacin

7.

Which of the following agent should be highly monitored in patients with kidney impairment?

a)

Levofloxacin

b)

Moxifloxacin

c)

Grepafloxacin

8.

Multivalent cation-containing products may reduce the absorption of fluoroquinolones.

a)

True

b)

False

9.

CIprofloxacin and pefloxacin may interact with theophylline through involvement of CYP450.

a)

True

b)

False

10.

Which of the agents have effect on cardiovascular?

a)

Levofloxacin

b)

Sparfloxacin

c)

Moxifloxacin

d)

Gatifloxacin

11.

What type of cardiovascular effect do some of the fluoroquinolone cause?

a)

Increased blood pressure

b)

Reduced heart rate

c)

Prolonged QTc interval