Article Contents ::
- 1 Details About Generic Salt :: Loperami
- 2 Main Medicine Class:: Antidiarrheal
- 3 (low-PEHR-uh-mide HIGH-droe-KLOR-ide) Diar-aid, Imodium, Imodium A-D, Kaopectate II Caplets, Maalox Anti-Diarrheal, Neo-Diaral, Pepto Diarrhea Control, Alti-Loperamide, Apo-Loperamide, Diarr-Eze, Novo-Loperamide, PMS-Loperamide Hydrochloride Class: Antidiarrheal
- 4 Drugs Class ::
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
Details About Generic Salt :: Loperami
Main Medicine Class:: Antidiarrheal
(low-PEHR-uh-mide HIGH-droe-KLOR-ide)
Diar-aid, Imodium, Imodium A-D, Kaopectate II Caplets, Maalox Anti-Diarrheal, Neo-Diaral, Pepto Diarrhea Control, Alti-Loperamide, Apo-Loperamide, Diarr-Eze, Novo-Loperamide, PMS-Loperamide Hydrochloride
Class: Antidiarrheal
Drugs Class ::
Action Slows intestinal motility, affects water and electrolyte movement through intestine, inhibits peristalsis, reduces daily fecal volume, increases viscosity and bulk density of stool, diminishes loss of fluid and electrolytes.
Indications for Drugs ::
Indications Control and symptomatic relief of acute non-specific or chronic diarrhea; reduction in volume of ileostomy output.
Drug Dose ::
Route/Dosage
Acute Diarrhea
ADULTS: PO 4 mg followed by 2 mg after each unformed stool; not to exceed 16 mg/24 hr. CHILDREN 8 TO 12 YR (> 30 KG): 2 mg tid. 6 to 8 YR (20 to 30 KG): 2 mg bid. 2 to 5 YR (13 to 20 KG): First day: 1 mg tid. May decrease to adjust for nutritional and hydration status after 24 hr; usually 0.1 mg/kg after each loose stool but do not exceed total first day dosing recommendations on any day.
Chronic Diarrhea
ADULTS: PO 4 to 8 mg qd or bid.
Contraindication ::
Contraindications Pseudomembranous colitis due to antibiotic use; acute diarrhea associated with organisms that penetrate intestinal wall (eg, toxigenic Escherichia coli, Salmonella, and Shigella); conditions in which constipation should be avoided; bloody diarrhea; fever; acute ulcerative colitis (potential for toxic megacolon).
Drug Precautions ::
Precautions
Pregnancy: Category B. Lactation: Undetermined. Children: Not recommended for children < 2 yr. Use with caution in young children. Acute ulcerative colitis: Agents that inhibit intestinal motility or delay intestinal transit time may induce toxic megacolon. Discontinue if abdominal distention or other untoward symptoms occur. Hepatic impairment: Hepatic coma may be precipitated in patients with advanced hepatorenal disease or hepatic dysfunction.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
CNS: Fatigue; drowsiness; dizziness. DERM: Rash. GI: Abdominal pain; distention or discomfort; constipation; nausea; vomiting; dry mouth.
Drug Mode of Action ::
Action Slows intestinal motility, affects water and electrolyte movement through intestine, inhibits peristalsis, reduces daily fecal volume, increases viscosity and bulk density of stool, diminishes loss of fluid and electrolytes.
Drug Interactions ::
Interactions None well documented.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies.
- Assess frequency and consistency of stools.
- Assess bowel sounds before and throughout course of therapy.
- Monitor I&O, fluid and electrolyte balance and skin turgor for signs of dehydration.
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Drug Storage/Management ::
Administration/Storage
- Administer as ordered, usually after each unformed stool.
- Store at room temperature.
Drug Notes ::
Patient/Family Education
- Instruct patient to record number and consistency of stools.
- Inform patient that medication may cause dry mouth. Encourage patient to drink plenty of clear fluids to help prevent dehydration that may accompany diarrhea.
- Advise patient to notify physician if diarrhea persists > 48 hr or if fever develops.
- Inform patient that drug may cause drowsiness or dizziness and to use caution while driving or performing other tasks requiring mental alertness.