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Nitazoxanide (Monograph)

Brand name: Alinia
Drug class:
Chemical name: 2-acetyloxy-N-(5-nitro-2-thiazolyl)benzamide
Molecular formula: C12H9N3 O5 S
CAS number: 55981-09-4

Medically reviewed by Drugs.com on Apr 10, 2024. Written by ASHP.

Introduction

Antiprotozoal; nitrothiazolyl-salicylamide derivative.1 17

Uses for Nitazoxanide

Cryptosporidiosis

Treatment of diarrhea caused by Cryptosporidium parvum in immunocompetent adults, adolescents, and children ≥1 year of age.1 134 Designated an orphan drug by FDA for treatment of cryptosporidiosis.13

Recommended as drug of choice for treatment of cryptosporidiosis.134

Although safety and efficacy not established for treatment of diarrhea caused by C. parvum in HIV-infected or other immunodeficient patients, nitazoxanide has been used for treatment of cryptosporidiosis in such individuals.1 CDC, NIH, IDSA, and others state that the most appropriate treatment for cryptosporidiosis in HIV-infected individuals is potent antiretroviral therapy (to restore immune function) and supportive care and symptomatic treatment of diarrhea.6 155 156 These experts state that adjunctive use of nitazoxanide can be considered for treatment of cryptosporidiosis in HIV-infected adults, adolescents, or children [off-label] receiving effective antiretroviral therapy; however, do not use nitazoxanide in HIV-infected patients not receiving antiretroviral therapy.155 156

Giardiasis

Treatment of diarrhea caused by Giardia intestinalis (also known as G. lamblia or G. duodenalis) in immunocompetent adults, adolescents, and children ≥1 year of age.1 Designated an orphan drug by FDA for treatment of intestinal giardiasis.13

Metronidazole, tinidazole, and nitazoxanide are the drugs of choice for treatment of giardiasis;134 alternatives include paromomycin (especially in pregnant women), furazolidone (no longer commercially available in US), or quinacrine (not commercially available in US).134 292

Safety and efficacy not established for treatment of diarrhea caused by Giardia in HIV-infected or other immunodeficient patients.1 CDC, NIH, and IDSA state that tinidazole and nitazoxanide are drugs of choice for treatment of giardiasis in HIV-infected infants and children [off-label] and metronidazole is the preferred alternative in these patients.156

Amebiasis

Has been used for treatment of amebiasis caused by Entamoeba [off-label].17 18 19 134 292 Designated an orphan drug by FDA for treatment of intestinal amebiasis.13

Regimen of choice for symptomatic intestinal amebiasis or extraintestinal disease is treatment with a nitroimidazole derivative (tinidazole or metronidazole) followed by treatment with a luminal amebicide (iodoquinol or paromomycin).134 292

Although nitazoxanide has been effective in some patients with mild to moderate intestinal amebiasis,17 18 134 292 data are limited and some clinicians state that additional study is needed.18 19

Isosporiasis (Cystoisosporiasis)

Has been used in some patients for treatment of isosporiasis [off-label] (also known as cystoisosporiasis) caused by Isospora belli (Cystoisospora belli).17 292

Co-trimoxazole is drug of choice for treatment of infections caused by I. belli (C. belli);134 155 156 292 pyrimethamine and ciprofloxacin are recommended alternatives.134 155

Although data are limited, some experts state that nitazoxanide is a potential alternative for treatment of isosporiasis (cystoisosporiasis) in HIV-infected infants and children [off-label] who cannot tolerate co-trimoxazole.156

Cestode (Tapeworm) Infections

Has been used for treatment of hymenolepiasis caused by Hymenolepis nana (dwarf tapeworm).14

Praziquantel is drug of choice for infections caused by H. nana;20 134 niclosamide (not commercially available in US) and nitazoxanide are recommended as alternatives.20 134

Nematode (Roundworm) Infections

Has been used for treatment of ascariasis caused by Ascaris lumbricoides.14 Albendazole, mebendazole, and ivermectin are the drugs of choice for ascariasis.134

Has been used for treatment of trichuriasis caused by Trichuris trichiura (whipworm).14 Albendazole is drug of choice for trichuriasis;134 recommended alternatives are mebendazole and ivermectin.134

Trematode (Fluke) Infections

Has been used for treatment of fascioliasis caused by Fasciola hepatica (sheep liver fluke).17 134

Triclabendazole is considered drug of choice for fascioliasis and bithionol (not commercially available in US) and nitazoxanide are recommended as alternatives.134

Nitazoxanide Dosage and Administration

Administration

Oral Administration

Administer orally twice daily with food.1

Do not use nitazoxanide 500-mg tablets in pediatric patients ≤11 years of age;1 amount of drug contained in the tablets exceeds recommended dosage in this age group.1

Reconstitution

Reconstitute powder for oral suspension at time of dispensing by adding 48 mL of water according to the manufacturer's directions.1 Tap the bottle to loosen the powder and add the water in 2 portions;1 shake vigorously after each addition.1

Reconstituted suspension contains 100 mg/5 mL.1

Shake suspension well prior to administration of each dose.1

Dosage

Nitazoxanide tablets and oral suspension are not bioequivalent.1

Pediatric Patients

Cryptosporidiosis
Oral

Children 1–3 years of age: 100 mg every 12 hours for 3 days.1 134

Children 4–11 years of age: 200 mg every 12 hours for 3 days.1 134

Children ≥12 years of age: 500 mg every 12 hours for 3 days.1 134

HIV-infected pediatric patients receiving optimized antiretroviral regimen: CDC, NIH, and IDSA recommend 100 mg twice daily in those 1–3 years of age, 200 mg twice daily in those 4–11 years of age, and 500 mg twice daily in those ≥12 years of age.156 Recommended duration is 3–14 days.156

Giardiasis
Oral

Children 1–3 years of age: 100 mg every 12 hours for 3 days.1 134

Children 4–11 years of age: 200 mg every 12 hours for 3 days.1 134

Children ≥12 years of age: 500 mg every 12 hours for 3 days.1 134

HIV-infected pediatric patients: CDC, NIH, and IDSA recommend 100 mg every 12 hours in those 1–3 years of age, 200 mg every 12 hours in those 4–11 years of age, and 500 mg every 12 hours in those ≥12 years of age.156 Recommended duration is 3 days.156

Isosporiasis (Cystoisosporiasis)†
Oral

HIV-infected pediatric patients: CDC, NIH, and IDSA recommend 100 mg every 12 hours in those 1–3 years of age, 200 mg every 12 hours in those 4–11 years of age, and 500 mg every 12 hours in those ≥12 years of age.156 Recommended duration is 3 days.156

Cestode (Tapeworm) Infections†
Hymenolepiasis†
Oral

Children 1–3 years of age: 100 mg twice daily for 3 days.14 292

Children 4–11 years of age: 200 mg twice daily for 3 days.14 292

Children ≥12 years of age: 500 mg twice daily for 3 days.292

Nematode (Roundworm) Infections†
Ascariasis†
Oral

Children 1–3 years of age: 100 mg twice daily for 3 days.14 292

Children 4–11 years of age: 200 mg twice daily for 3 days.14 292

Children ≥12 years of age: 500 mg twice daily for 3 days.292

Trichuriasis†
Oral

Children 1–3 years of age: 100 mg twice daily for 3 days.14

Children 4–11 years of age: 200 mg twice daily for 3 days.14

Trematode (Fluke) Infections†
Fascioliasis†
Oral

Children 1–3 years of age: 100 mg twice daily for 7 days.134

Children 4–11 years of age: 200 mg twice daily for 7 days.134

Children ≥12 years of age: 500 mg twice daily for 7 days.134

Adults

Cryptosporidiosis
Oral

500 mg every 12 hours for 3 days.1 134

HIV-infected adults receiving optimized antiretroviral regimen: CDC, NIH, and IDSA recommend 0.5–1 g twice daily for 14 days.155

Giardiasis
Oral

500 mg every 12 hours for 3 days.1 134

Cestode (Tapeworm) Infections†
Hymenolepiasis†
Oral

500 mg twice daily for 3 days.292

Trematode (Fluke) Infections†
Fascioliasis†
Oral

500 mg twice daily for 7 days.134

Cautions for Nitazoxanide

Contraindications

Warnings/Precautions

General Precautions

Immunodeficiency

Has not been more effective than placebo for treatment of diarrhea caused by C. parvum in HIV-infected or other immunodeficient individuals.1

Not evaluated for treatment of diarrhea caused by Giardia in HIV-infected or other immunodeficient individuals.1

Specific Populations

Pregnancy

Data not available on use of nitazoxanide in pregnant women to inform a drug-associated risk.1

In animal reproduction studies, no evidence of teratogenicity or fetotoxicity when nitazoxanide was given to pregnant rats and rabbits during organogenesis at exposures 30 and 2 times, respectively, the human exposure at recommended human dosage of 500 mg twice daily based on body surface area.1

Lactation

Not known whether distributed into human milk, affects milk production, or affects breast-fed child.1

Consider developmental and health benefits of breast-feeding along with the mother's clinical need for nitazoxanide and potential adverse effects on the breast-fed infant from the drug or the underlying maternal condition.1

Pediatric Use

Safety and efficacy not established in children <1 year of age.1

Nitazoxanide oral suspension: Safety and efficacy for treatment of diarrhea caused by C. parvum or Giardia established in pediatric patients 1–17 years of age.1

Nitazoxanide tablets: Safety and efficacy for treatment of diarrhea caused by C. parvum or Giardia established in pediatric patients 12–17 years of age.1 Do not use the 500-mg tablets in pediatric patients ≤11 years of age since the tablets contain a greater amount of the drug than is recommended in this age group.1

Geriatric Use

Experience in those ≥65 years of age insufficient to determine whether they respond differently than younger individuals.1

Consider the greater frequency of decreased hepatic, renal, and/or cardiac function and of concomitant disease or drug therapy in this age group.1

Hepatic Impairment

Use with caution;17 pharmacokinetics not evaluated.1

Renal Impairment

Use with caution;17 pharmacokinetics not evaluated.1

Common Adverse Effects

Abdominal pain, headache, chromaturia, nausea.1

Drug Interactions

Protein-bound Drugs

Possible pharmacokinetic interactions with other highly protein-bound drugs; monitor closely if used concomitantly with highly protein-bound drugs with a narrow therapeutic index.1 (See Specific Drugs under Interactions.)

Drugs Metabolized by Hepatic Microsomal Enzymes

Does not inhibit CYP isoenzymes.1

Specific Drugs

Drug

Interaction

Comments

Warfarin

Possible competition for protein binding sites1

Avoid concomitant use1

Nitazoxanide Pharmacokinetics

Absorption

Bioavailability

Following oral administration, nitazoxanide is rapidly hydrolyzed to an active metabolite, tizoxanide, which is converted to tizoxanide glucuronide.1

Peak plasma concentrations of tizoxanide and tizoxanide glucuronide usually attained within 1–5 and 2–8 hours, respectively;1 nitazoxanide undetectable in plasma.1

The tablets and oral suspension are not bioequivalent.1 Bioavailability of the oral suspension is 70% relative to that of the tablet.1

Food

Administration of nitazoxanide with food increases tizoxanide and tizoxanide glucuronide AUCs.1

Distribution

Plasma Protein Binding

Tizoxanide: >99%.1

Elimination

Metabolism

Rapidly hydrolyzed to tizoxanide;1 tizoxanide subsequently undergoes conjugation, primarily by glucuronidation.1

Elimination Route

Tizoxanide eliminated in urine, bile, and feces;1 tizoxanide glucuronide eliminated in urine and bile.1

Half-life

Nitazoxanide: 6 minutes.17

Tizoxanide: 1.2–1.5 hours after single dose with food;17 1.8–6.4 hours after repeated doses with food.

Tizoxanide glucuronide: 1.9–2.9 hours after single dose with food;17 3.5–5.6 hours after repeated doses with food.17

Special Populations

Pharmacokinetics not studied in patients with hepatic or renal impairment.1

Stability

Storage

Oral

For Suspension

25°C (may be exposed to 15–30°C).1

After reconstitution, store at room temperature;1 discard after 7 days.1

Tablets

25°C (may be exposed to 15–30°C).1

Actions and Spectrum

Advice to Patients

Preparations

Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.

Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.

Nitazoxanide

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Oral

For suspension

100 mg/5 mL

Alinia

Romark

Tablets

500 mg

Alinia

Romark

AHFS DI Essentials™. © Copyright 2024, Selected Revisions April 10, 2024. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814.

† Off-label: Use is not currently included in the labeling approved by the US Food and Drug Administration.

References

1. Romark Laboratories. Alinia (nitazoxanide) tablets and powder for oral suspension prescribing information. Tampa, FL: 2017 Apr.

2. Amadi B, Mwiya M, Musuku J et al. Effect of nitazoxanide on morbidity and mortality in Zambian children with cryptosporidiosis: a randomised controlled study. Lancet. 2002; 360:1375-80. http://www.ncbi.nlm.nih.gov/pubmed/12423984?dopt=AbstractPlus

3. Rossignol J-F A, Ayoub A, Ayers MS. Treatment of diarrhea caused by Cryptosporidium parvum: a prospective randomized, double-blind, placebo-controlled study of nitazoxanide. J Infect Dis. 2001; 184:103-6. http://www.ncbi.nlm.nih.gov/pubmed/11398117?dopt=AbstractPlus

5. Scott KG, Meddings JB, Kirk DR et al. Intestinal infection with Giardia spp. reduces epithelial barrier function in a myosin light chain kinase-dependent fashion. Gastroenterology. 2002; 123:1179-90. http://www.ncbi.nlm.nih.gov/pubmed/12360480?dopt=AbstractPlus

6. Chen XM, Keithly JS, Paya CV et al. Cryptosporidiosis. N Engl J Med. 2002; 346:1723-31. http://www.ncbi.nlm.nih.gov/pubmed/12037153?dopt=AbstractPlus

7. Kosek M, Alcantara C, Lima AAM et al. Cryptosporidiosis: an update. Lancet Infect Dis. 2001; 1:262-9. http://www.ncbi.nlm.nih.gov/pubmed/11871513?dopt=AbstractPlus

9. Centers for Disease Control and Prevention. Diagnosis and management of foodborne illness. A primer for physicians. MMWR Morb Mortal Wkly Rep. 2001; 50(No. RR-2):1-69. http://www.ncbi.nlm.nih.gov/pubmed/11215787?dopt=AbstractPlus

10. Adagu IS, Nolder D, Warhurst DC et al. In vitro activity of nitazoxanide and related compounds against isolates of Giardia intestinalis, Entamoeba histolytica, and Trichomonas vaginalis . J Antimicrob Chemother. 2002; 49:103-14. http://www.ncbi.nlm.nih.gov/pubmed/11751773?dopt=AbstractPlus

11. Romark Laboratories, Tampa, FL: personal communication.

13. Food and Drug Administration. Search orphan drug designations and approvals. From FDA website. Accessed 2019 Feb 15. https://www.accessdata.fda.gov/scripts/opdlisting/oopd/

14. Juan JO, Lopez Chegne N, Gargala G et al. Comparative clinical studies of nitazoxanide, albendazole and praziquantel in the treatment of ascariasis, trichuriasis and hymenolepiasis in children from Peru. Trans R Soc Trop Med Hyg. 2002; 96:193-6. http://www.ncbi.nlm.nih.gov/pubmed/12055813?dopt=AbstractPlus

17. Reynoso D, White AC. Nitazoxanide. In: Grayson ML, ed. Kucers' the use of antibiotics: a clinical review of antibacterial, antifungal, antiparasitic, and antiviral drugs. 7th ed. Boca Raton, FL: CRC Press; 2018:3162-74.

18. Rossignol JF, Kabil SM, El-Gohary Y et al. Nitazoxanide in the treatment of amoebiasis. Trans R Soc Trop Med Hyg. 2007; 101:1025-31. http://www.ncbi.nlm.nih.gov/pubmed/17658567?dopt=AbstractPlus

19. Gonzales MLM, Dans LF, Sio-Aguilar J. Antiamoebic drugs for treating amoebic colitis. Cochrane Database Syst Rev. 2019; 1:CD006085. http://www.ncbi.nlm.nih.gov/pubmed/30624763?dopt=AbstractPlus

20. Centers for Disease Control and Prevention. Hymenolepsis. From CDC website. Accessed April 1, 2019. https://www.cdc.gov/parasites/hymenolepis/health_professionals/index.html

134. Anon. Drugs for parasitic infections. Treat Guidel Med Lett. 2013; 11:e1-31.

155. Panel on Opportunistic Infection in HIV-infected Adults and Adolescents. Guidelines for the prevention and treatment of opportunistic infections in HIV-infected adults and adolescents: recommendations from the Centers for Disease Control and Prevention, the National Institutes of Health, and the HIV Medicine Association of the Infectious Diseases Society of America (Accessed February 15, 2019). Updates may be available at HHS AIDS Information (AIDSinfo) website https://aidsinfo.nih.gov/contentfiles/lvguidelines/adult_oi.pdf

156. Panel on Opportunistic Infections in HIV-exposed and HIV-infected Children. Guidelines for the prevention and treatment of opportunistic infections in HIV-exposed and HIV-infected children: recommendations from the National Institutes of Health, Centers for Disease Control and Prevention, the HIV Medicine Association of the Infectious Diseases Society of America, and the Pediatric Infectious Diseases Society. (Accessed February 15, 2019). Updates may be available at HHS AIDS Information (AIDSinfo) website https://aidsinfo.nih.gov/contentfiles/lvguidelines/oi_guidelines_pediatrics.pdf

292. American Academy of Pediatrics. Red Book: 2018-2021 Report of the Committee on Infectious Diseases. 31st ed. Itasca, IL: American Academy of Pediatrics; 2018.