Givotan Actions

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How do you administer this medicine?
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Actions of Givotan in details

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The antiprotozoal activity of Givotan is believed to be due to interference with the pyruvate:ferredoxin oxidoreductase (PFOR) enzyme-dependent electron transfer reaction which is essential to anaerobic energy metabolism. Studies have shown that the PFOR enzyme from Giardia lamblia directly reduces Givotan by transfer of electrons in the absence of ferredoxin. The DNA-derived PFOR protein sequence of Cryptosporidium parvum appears to be similar to that of Giardia lamblia. Interference with the PFOR enzyme-dependent electron transfer reaction may not be the only pathway by which Givotan exhibits antiprotozoal activity.

How should I take Givotan?

Dosing

The dose of Givotan will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of Givotan. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

It is important to take Givotan with food.

It is very important to shake the oral suspension for of the medicine well before measuring each dose.

For the oral suspension dosage form: Use a specially marked measuring syringe or spoon to measure each dose accurately. The average household teaspoon may not hold the right amount of liquid.

Missed Dose

If you miss a dose of Givotan, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.

Storage

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

The suspension may be stored for 7 days. Any unused suspension must be disposed of after 7 days.

Givotan administration

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Take Givotan exactly as directed by your doctor. If you do not understand these instructions, ask your pharmacist, nurse, or doctor to explain them to you.

Take Givotan with food.

Shake the suspension well before measuring a dose. To ensure that you get the correct dose, measure the suspension with a dose-measuring spoon, dropper, or cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist where you can get one.

Store the suspension at room temperature. The suspension may be stored for 7 days, after which any unused portion must be discarded.

Givotan pharmacology

Mechanism of Action

Givotan is an antiprotozoal.

Pharmacokinetics

Absorption

Single Dosing:

Following oral administration of Givotan tablets or oral suspension, the parent drug, Givotan, is not detected in plasma. The pharmacokinetic parameters of the metabolites, tizoxanide and tizoxanide glucuronide are shown in Tables 2 and 3 below.

Table 2. Mean (+/- SD) plasma pharmacokinetic parameters of tizoxanide and tizoxanide glucuronide following administration of a single dose of one 500 mg Givotan tablets with food to subjects ≥12 years of age

Tizoxanide

Tizoxanide Glucuronide

Age

Cmax (μg/mL)

*Tmax

(hr)

AUCԏ

(μg•hr/mL)

Cmax

(μg/mL)

*Tmax

(hr)

AUCԏ

(μg•hr/mL)

12-17 years

≥18 years

9.1 (6.1)

10.6 (2.0)

4.0 (1-4)

3.0 (2-4)

39.5 (24.2)

41.9 (6.0)

7.3 (1.9)

10.5 (1.4)

4.0 (2-8)

4.5 (4-6)

46.5 (18.2)

63.0 (12.3)

* Tmax is given as a Mean (Range)

Table 3. Mean (+/- SD) plasma pharmacokinetic of tizoxanide and tizoxanide glucuronide parameter values following administration of a single dose of Givotan for oral suspension with food to subjects ≥1 year of age

Tizoxanide

Tizoxanide Glucuronide

Age

Dose

Cmax (μg/mL)

*Tmax

(hr)

AUCinf (μg•hr/mL)

Cmax (μg/mL)

*Tmax

(hr)

AUCinf (μg•hr/mL)

1-3 years

100 mg

3.11 (2.0)

3.5 (2-4)

11.7 (4.46)

3.64 (1.16)

4.0 (3-4)

19.0 (5.03)

4-11 years

200 mg

3.00 (0.99)

2.0 (1-4)

13.5 (3.3)

2.84 (0.97)

4.0 (2-4)

16.9 (5.00)

≥18 years

500 mg

5.49 (2.06)

2.5 (1-5)

30.2 (12.3)

3.21 (1.05)

4.0 (2.5-6)

22.8 (6.49)

* Tmax is given as a Mean (Range)

Multiple dosing:

Following oral administration of a single Givotan tablet every 12 hours for 7 consecutive days, there was no significant accumulation of Givotan metabolites tizoxanide or tizoxanide glucuronide detected in plasma.

Bioavailability:

Givotan for oral suspension is not bioequivalent to Givotan tablets. The relative bioavailability of the suspension compared to the tablet was 70%.

When Givotan tablets are administered with food, the AUCԏ of tizoxanide and tizoxanide glucuronide in plasma is increased almost two-fold and the Cmax is increased by almost 50%.

When Givotan for oral suspension was administered with food, the AUCԏ of tizoxanide and tizoxanide glucuronide increased by about 45-50% and the Cmax increased by ≤10%.

Givotan tablets and Givotan for oral suspension were administered with food in clinical trials and hence they are recommended to be administered with food.

Distribution

In plasma, more than 99% of tizoxanide is bound to proteins.

Elimination

Metabolism

Following oral administration in humans, Givotan is rapidly hydrolyzed to an active metabolite, tizoxanide (desacetyl-Givotan). Tizoxanide then undergoes conjugation, primarily by glucuronidation.

Excretion

Tizoxanide is excreted in the urine, bile and feces, and tizoxanide glucuronide is excreted in urine and bile. Approximately two-thirds of the oral dose of Givotan is excreted in the feces and one-third in the urine.

Specific Populations

Pediatric Patients

The pharmacokinetics of tizoxanide and tizoxanide glucuronide following administration of Givotan tablets in pediatric patients 12-17 years of age are provided above in Table 2. The pharmacokinetics of tizoxanide and tizoxanide glucuronide following administration of Givotan for oral suspension in pediatric patients 1-11 years of age are provided above in Table 3.

Drug Interaction Studies

In vitro studies demonstrated that tizoxanide has no significant inhibitory effect on cytochrome P450 enzymes.

Microbiology

Mechanism of Action

The antiprotozoal activity of Givotan is believed to be due to interference with the pyruvate:ferredoxin oxidoreductase (PFOR) enzyme-dependent electron transfer reaction which is essential to anaerobic energy metabolism. Studies have shown that the PFOR enzyme from G. lamblia directly reduces Givotan by transfer of electrons in the absence of ferredoxin. The DNA-derived PFOR protein sequence of C. parvum appears to be similar to that of G. lamblia.

Interference with the PFOR enzyme-dependent electron transfer reaction may not be the only pathway by which Givotan exhibits antiprotozoal activity.

Resistance

A potential for development of resistance by C. parvum or G. lamblia to Givotan has not been examined.

Antimicrobial Activity

Givotan and its metabolite, tizoxanide, are active in vitro in inhibiting the growth of (i) sporozoites and oocysts of C. parvum and (ii) trophozoites of G. lamblia.

Susceptibility Test Methods

For protozoa such as C. parvum and G. lamblia, standardized tests for use in clinical microbiology laboratories are not available.


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References

  1. DailyMed. "NITAZOXANIDE: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
  2. NCIt. "Nitazoxanide: NCI Thesaurus (NCIt) provides reference terminology for many systems. It covers vocabulary for clinical care, translational and basic research, and public information and administrative activities.". https://ncit.nci.nih.gov/ncitbrowser... (accessed September 17, 2018).
  3. EPA DSStox. "Nitazoxanide: DSSTox provides a high quality public chemistry resource for supporting improved predictive toxicology.". https://comptox.epa.gov/dashboard/ds... (accessed September 17, 2018).

Reviews

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Information checked by Dr. Sachin Kumar, MD Pharmacology

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