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Praziquantel (Biltricide)

Category:

  • Miscellaneous

Description:

  • Anthelmintic

Indications:

  • Schistosomiasis caused by Schistosoma spp. pathogenic to humans

  • Clonorchiasis and opisthorchiasis (liver flukes)

  • Cysticercosis (non FDA approved)

  • Intestinal cestode (tapeworm) infections (non FDA approved)

Contraindications:

  • Ocular cysticercosis

Precautions:

  • Pregnancy category B; do not nurse on day of treatment and during the subsequent 72 hours

  • Children <4 years

  • Cerebral cysticercosis (hospitalize patient for duration of therapy)

Adverse Reactions (Side Effects):

  • CNS: dizziness, drowsiness, fever, headache

  • GI: abdominal discomfort, minimal increases in liver enzymes

  • SKIN: urticaria

  • MISC: malaise

 

 

Dosage:

Administered orally

  • Adult and child:  

    • Schistosomiasis: PO 20 mg/kg/dose 2-3 times daily for 1 day at 4-6 hour intervals

    • Clonorchiasis and opisthorchiasis: PO 75 mg/kg/day divided every 8 hours for 1-2 days

    • Cysticercosis: PO 50 mg/kg/day divided every 8 hours for 14 days (administer steroids prior to starting praziquantel for neurocysticercosis)

    • Cestodes: PO 10-20 mg/kg as a single dose (25 mg/kg for Hymenolepsis nana)

Special considerations:

  • Swallow tablets unchewed with some liquid during meals

  • May cause drowsiness

  • Use caution driving or performing tasks requiring mental alertness

The information contained here is an abbreviated summary. For more detailed and complete information, consult the manufacturer's product information sheets or standard textbooks.

Source: Operational Medicine 2001,  Health Care in Military Settings, NAVMED P-5139, May 1, 2001, Bureau of Medicine and Surgery, Department of the Navy, 2300 E Street NW, Washington, D.C., 20372-5300

OB-GYN 101: Introductory Obstetrics & Gynecology
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