Antidiazox Overdose

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What happens if I overdose Antidiazox?

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Antidiazox suspension:

Store Antidiazox suspension at 77 degrees F (25 degrees C). Brief storage at temperatures between 58 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Throw away any unused medicine after 7 days. Keep Antidiazox suspension out of the reach of children and away from pets.

Overdose of Antidiazox in details

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Limited information on Antidiazox overdosage is available. Single oral doses of up to 4000 mg Antidiazox have been administered to healthy adult volunteers without significant adverse effects. In the event of overdose, gastric lavage may be appropriate soon after oral administration. Patients should be observed and given symptomatic and supportive treatment. There is no specific antidote for overdose with Antidiazox. Because tizoxanide is highly protein bound (>99.9%), dialysis is unlikely to significantly reduce plasma concentrations of the drug.

What should I avoid while taking Antidiazox?

There are no restrictions on food, beverages, or activity during treatment with Antidiazox unless otherwise directed by your doctor.

Antidiazox warnings

Antidiazox should be taken with food. Diabetic patients should be aware that the oral suspension contains 1.48 g of sucrose/5 ml.

What should I discuss with my healthcare provider before taking Antidiazox?

Some medical conditions may interact with Antidiazox suspension. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Antidiazox suspension. Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Antidiazox suspension may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Antidiazox precautions

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Nonclinical Toxicology

Carcinogenesis, Mutagenesis, Impairment Of Fertility

Carcinogenesis

Long-term carcinogenicity studies have not been conducted.

Mutagenesis

Antidiazox was not genotoxic in the Chinese hamster ovary (CHO) cell chromosomal aberration assay or the mouse micronucleus assay. Antidiazox was genotoxic in one tester strain (TA 100) in the Ames bacterial mutation assay.

Impairment Of Fertility

Antidiazox did not adversely affect male or female fertility in the rat at 2400 mg/kg/day (approximately 20 times the clinical adult dose adjusted for body surface area).

Use In Specific Populations

Pregnancy

Risk Summary

There are no data with Antidiazox in pregnant women to inform a drug-associated risk. No teratogenicity or fetotoxicity was observed in animal reproduction studies with administration of Antidiazox to pregnant rats and rabbits during organogenesis at exposures 30 and 2 times, respectively, the exposure at the maximum recommended human dose of 500 mg twice daily based on body surface area (BSA).

In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.

Data

Animal Data

Antidiazox was administered orally to pregnant rats at doses of 0, 200, 800 or 3200 mg/kg/day on gestation days 6 to 15. Antidiazox produced no evidence of systemic maternal toxicity when administered once daily via oral gavage to pregnant female rats at levels up to 3200 mg/kg/day during the period of organogenesis.

In rabbits, Antidiazox administered at doses of 0, 25, 50, or 100 mg/kg/day on gestation days 7 to 20.

Oral treatment of pregnant rabbits with Antidiazox during organogenesis resulted in minimal maternal toxicity and no external fetal anomalies.

Lactation

Risk Summary

No information regarding the presence of Antidiazox in human milk, the effects on the breastfed infant, or the effects on milk production is available. The development and health benefits of breastfeeding should be considered along with the mother's clinical need for Antidiazox and any potential adverse effects on the breastfed infant from Antidiazox or from the underlying maternal condition.

Pediatric Use

The safety and efficacy of Antidiazox for

Oral Suspension for the treatment of diarrhea caused by

G. lamblia or C. parvum in pediatric patients 1 to 11 years of age has been established based on three (3) randomized, controlled studies with 104 pediatric subjects treated with Antidiazox for

Oral Suspension 100 mg/5 mL. Furthermore, the safety and efficacy of Antidiazox for

Oral Suspension for the treatment of diarrhea caused by

G. lamblia or C. parvum in pediatric patients 12 to 17 years of age has been established based on two (2) randomized controlled studies with 44 pediatric subjects treated with Antidiazox for

Oral Suspension 100 mg/5 mL.

The safety and efficacy of Antidiazox Tablets for the treatment of diarrhea caused by G. lamblia or C. parvum in pediatric patients 12 to 17 years of age has been established based on three (3) randomized controlled studies with 47 pediatric subjects treated with Antidiazox Tablets 500 mg.

A single Antidiazox Tablet contains a greater amount of Antidiazox than is recommended for use in pediatric patients 11 years or younger..

Safety and efficacy of Antidiazox for

Oral Suspension in pediatric patients less than one year of age has not been studied.

Geriatric Use

Clinical studies of Antidiazox Tablets and Antidiazox for

Oral Suspension did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. In general, the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy in elderly patients should be considered when prescribing Antidiazox Tablets and Antidiazox for

Oral Suspension.

Renal And Hepatic Impairment

The pharmacokinetics of Antidiazox in patients with compromised renal or hepatic function has not been studied.

HIV-Infected Or Immunodeficient Patients

Antidiazox Tablets and Antidiazox for

Oral Suspension have not been studied for the treatment of diarrhea caused by G. lamblia in HIV-infected or immunodeficient patients. Antidiazox Tablets and Antidiazox for

Oral Suspension have not been shown to be superior to placebo for the treatment of diarrhea caused by C. parvum in HIV-infected or immunodeficient patients.

What happens if I miss a dose of Antidiazox?

Take the missed dose as soon as you remember. If you do not remember until it is time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take a double dose of the medication.


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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. DrugBank. "NITAZOXANIDE". http://www.drugbank.ca/drugs/DB00507 (accessed September 17, 2018).
  3. MeSH. "Antiparasitic Agents". https://www.ncbi.nlm.nih.gov/mesh/68... (accessed September 17, 2018).

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Information checked by Dr. Sachin Kumar, MD Pharmacology

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