Famoloc
Generic Name
famoloc-40-mg-suspension
Manufacturer
Square Pharmaceuticals Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
Variant | Unit Price | Strip Price |
---|---|---|
famoloc 40 mg suspension | ৳ 50.00 | N/A |
Description
Overview of the medicine
Famoloc-40-mg-suspension contains Famotidine, an H2-receptor antagonist that reduces stomach acid production. It is used to treat and prevent various conditions like stomach and duodenal ulcers, gastroesophageal reflux disease (GERD), and Zollinger-Ellison Syndrome.
Uses & Indications
Dosage
Adults
Active Duodenal Ulcer: 40 mg orally once daily at bedtime or 20 mg twice daily for 4-8 weeks. GERD: 20-40 mg orally twice daily for up to 12 weeks. Zollinger-Ellison Syndrome: Initial 20 mg every 6 hours; dosage may be increased up to 160 mg every 6 hours. Pediatric (1-16 years) GERD: 1 mg/kg/day divided twice daily, max 40 mg twice daily.
Elderly
No specific dose adjustment is generally required, but caution is advised in elderly patients, especially those with renal impairment, due to potential for increased plasma levels.
Renal_impairment
In patients with creatinine clearance <30 mL/min, the dose should be reduced to 20 mg at bedtime or the dosing interval should be prolonged to every other day.
How to Take
For oral administration. Shake the bottle well before each use. Can be taken with or without food. Use a measuring device for accurate dosing.
Mechanism of Action
Famotidine competitively blocks histamine at the H2-receptors on the gastric parietal cells, leading to a reduction in gastric acid secretion (both basal and stimulated) and pepsin output. This action helps to heal ulcers and reduce symptoms of acid reflux.
Pharmacokinetics
Onset
Within 1 hour
Excretion
Primarily renal; 65-70% of an oral dose is excreted unchanged in urine.
Half life
2.5-3.5 hours (increases in renal impairment)
Absorption
Rapidly absorbed from the gastrointestinal tract. Bioavailability is approximately 40-45% after oral administration and is not significantly affected by food.
Metabolism
Minimal hepatic metabolism, forming an inactive sulfoxide metabolite.
Side Effects
Contraindications
- Hypersensitivity to famotidine or other H2-receptor antagonists (e.g., cimetidine, ranitidine, nizatidine).
- Acute porphyria (theoretical risk, but generally avoided).
Drug Interactions
Cefpodoxime
Reduced absorption due to increased gastric pH.
Atazanavir, Rilpivirine
Reduced plasma concentrations of these antiretroviral drugs may occur. Concomitant use with famotidine should be avoided or carefully monitored.
Ketoconazole, Itraconazole
Famotidine can significantly increase gastric pH, leading to reduced absorption of these drugs. Administer these drugs at least 2 hours before famotidine.
Calcium Carbonate/Magnesium Hydroxide (antacids)
Separate administration by at least 1-2 hours to avoid potential interference with famotidine absorption.
Storage
Store below 30°C in a dry place, away from direct sunlight and moisture. Do not freeze. Keep out of reach of children.
Overdose
Symptoms of overdose may include hypotension, tachycardia, vomiting, and central nervous system effects (e.g., restlessness, confusion). Management should be symptomatic and supportive, including gastric lavage or activated charcoal if recent ingestion. Hemodialysis may be considered for severe renal impairment.
Pregnancy & Lactation
Pregnancy Category B. Famotidine should be used during pregnancy only if clearly needed. Famotidine is excreted in human breast milk; therefore, caution should be exercised when administered to a nursing mother.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
24-36 months from manufacturing date, check specific product label for expiry. Once reconstituted, typically 30 days.
Availability
Pharmacies, Hospitals
Approval Status
Approved by regulatory authorities
Patent Status
Off-patent
WHO Essential Medicine
YesClinical Trials
Famotidine has undergone extensive clinical trials demonstrating its efficacy and safety in the treatment of peptic ulcers, GERD, and hypersecretory conditions. Studies have shown comparable efficacy to other H2-blockers and proton pump inhibitors in certain indications.
Lab Monitoring
- Regular monitoring of renal function in patients with kidney impairment.
- Liver function tests (LFTs) may be considered during prolonged therapy or if liver enzyme elevations occur.
Doctor Notes
- Ensure to rule out gastric malignancy before starting therapy for suspected gastric ulcer, as symptomatic response to famotidine does not preclude the presence of malignancy.
- Consider dose reduction in patients with moderate to severe renal impairment to prevent accumulation and potential adverse effects.
- Counsel patients on lifestyle modifications to complement drug therapy for GERD and peptic ulcer disease.
Patient Guidelines
- Take the medicine exactly as prescribed by your doctor.
- Do not stop taking the medication abruptly, even if symptoms improve, without consulting your doctor.
- Report any new or worsening symptoms, or unusual side effects, to your doctor.
Missed Dose Advice
If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and resume your regular dosing schedule. Do not take a double dose to make up for a missed one.
Driving Precautions
Famoloc may cause dizziness in some individuals. Patients should be advised to exercise caution when driving or operating machinery until they know how the medication affects them.
Lifestyle Advice
- Avoid foods and drinks that trigger heartburn or indigestion (e.g., spicy foods, caffeine, alcohol, fatty foods).
- Elevate the head of your bed if you experience nighttime GERD symptoms.
- Maintain a healthy weight, avoid smoking, and reduce stress to manage acid reflux.
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