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Wednesday, April 2, 2014

Cetirizine


Indication:

Seasonal Allergic Rhinitis, Perennial Allergic Rhinitis, Chronic Idiopathic Urticaria, and Pruritus. It is also used in allergen induced asthma.

Dosage and Administration:

Administered with or without food. Adults and Children 6 years and older : Tablet: 1 tablet daily. Syrup: 2 teaspoonfuls once daily or 1 teaspoonful twice daily. In patients with decreased renal function (Creatinine clearance 11-31 ml/min), patients on emodialysis (Creatinine clearance less than 7 ml/min) and in hepatically impaired atients , a dose of 1/2 tablet or 1 teaspoonful once daily is recommended. Children 2-6 years : Syrup: 1 teaspoonful once daily or 1/2 teaspoonful twice daily. Children 6 months - <2 years : Syrup: 1/2 teaspoonful once daily. The mg once daily for three consecutive days.Giardiasis - 400 mg once daily for five days. Hydatid disease (Echinococcosis) - 400 mg twice daily for 28 days. For cystic echinococcosis the 28-days course may be repeated after 14 days without treatment to a total of three treatment cycles. For alveolar echinococcosis, 400 mg twice daily for 28 days followed by 14 days without treatment may need to continue for months or years.

Contraindication & Precaution:

Should only be used in the treatment of echinococcosis if there is constant medical supervision with regular monitoring of serum transaminase concentrations and of leucocyte and platelet counts.

Side Effect:

Epigastric pain, diarrhoea, headache, nausea, vomiting, dizziness, constipation, pruritis & dry mouth.

Use in Pregnancy & Lactation:

 Should not be administered during pregnancy & in women thought to be pregnant.

Pediatric Use:

For children of 12 months & above.

Preparation:

 400 mg Tablet & 200 mg / 5ml Suspension.

Ketotifen


Indication

Symptomatic treatment of allergic conditions including rhinitis and conjunctivitis. Prophylactic treatment of
Bronchial asthma

Dosage and Administration

Adults : 1 mg twice daily with food. If necessary the dose may be increased to 2 mg twice daily in severe cases.
Children above 3 years: 1 mg twice daily with food. Patients known to be easily sedated should begin treatment with 0.5 to 1 mg at night for the first few days or as directed by the physician. Use in elderly: Same as adult dose or as advised by the physician.

Contraindication and Precaution

A reversible fall in the platelet count has been observed in a few patients receiving Ketotifen concomitantly should not be instilled while the patient is wearing lenses.

Side Effect

1-2%: Burning/stinging, punctuate corneal epithelial erosion. <1%: Blurring of vision upon drug instillation, dry eyes, eyelid disorder, conjunctivitis, eye pain, photophobia, subconjunctival haemorrhage.

Use in Pregnancy & Lactation

Systemic levels after ocular administration are much lower than after oral use. Caution should be exercised when prescribing to pregnant women.

Use in Children

Children under 3 years of age: Consult with a doctor.

Preparation

 0.025% Eye Drops.

Thursday, March 27, 2014

Cefuroxime




Indication

Cefuroxime is indicated  in the treatment  of
1. Upper respiratory tract infections: For example, ear, nose and throat infections such as otitis media, sinusitis, tonsillitis and pharyngitis.
2. Lower respiratory tract infections: For example, acute bronchitis, acute exacerbations of chronic bronchitis and pneumonia.
3. Skin and sft tissue infections: Such as furunculosis, pyoderma and impetigo.
4. Genilo-urinary tract infections: Such as pyelonephritis, urethritis and cystitis.
5. Gonorrhoea: Acute uncomplicated gonococcal urethritis and cervicitis.
6. Early lyme disease and subsequent prevention of late Lyme disease.

Pharmacology

Cefuroxime is a well-characterized and effective antibacterial agent, which has broad-spectrum  bactericidal activity against a wide range of common pathogens, including β-lactamase producing strains. Cefuroxime has good stability to bacterial β-lactamase and consequently, is active against many ampicillin-resistant and amoxycillin-resistant strains.

Composition  

Cefuroxime 125 mg tablet: Each film coated tablet contains Cefuroxime 125 mg as Cefuroxime axetil BP.
Cefuroxime 250 mg tablet: Each film coated tablet contains Cefuroxime 250 mg as Cefuroxime axetil BP.
Cefuroxime 500 mg tablet: Each film coated tablet contains Cefuroxime 500 mg as Cefuroxime axetil BP.
Cefuroxime powder for suspension (70 ml): Each 5 ml reconstituted suspension contains 125 mg Cefuroxime, as Cefuroxime axetil BP.
Cefuroxime 750 mg IM/IV injection: Each vial contains Cefuroxime 750 mg, as Cefuroxime sodium BP.
Cefuroxime 1.5 gm IV injection: Each vial contains Cefuroxime 1.5 gm, as Cefuroxime sodium BP.

Dosage and Administration
 
Adults: Most infections well respond to 250 mg b.i.d. In mild to moderate lower respiratory tract infections e.g bronchitis 250 mg b.i.d. should be given. For more severe lower respiratory tract infections or if pneumonia is suspected then 500 mg b.i.d. should be given.
For urinary tract infections a dose of 125 mg b.i.d. is usually adequate, in pyelonephritis the recommended dose is 250 mg b.i.d. A single dose of one gram is recommended for the treatment of uncomplicated gonorrhea.
Lyme disease in adults and children over the age of 12 years: The recommended dose is 500 mg b.i.d. for 20 days.
Children: The usual dose is 125 mg b.i.d. or 10 mg/kg b.i.d. to a maximum of 250 mg daily.
For otitis media, in children less than two years of age the usual dosage is 125 mg b.i.d. or 10 mg/kg b.i.d. to a maximum of 250 mg daily and in children over two years of age 250 mg b.i.d. or 15 mg/kg b.i.d. to a maximum of 500 mg daily.
There is no experience in children under three months of age. The usual course of therapy in seven days. Cefuroxime should be taken after food for optimum absorption.

Parental Dosage

Adults: Cefuroxime 750 mg to 1.5 g IM or IV every 8 hourly, usually 50 to 10 days.
Preoperative prophylaxis: For clean contaminated or potentially contaminated surgical procedures, administer 1.5 g IV prior to surgery ( half to one hour before ). Thereafter, give 750 mg iV or IM every 8 hours when the procedure is prolonged.
Infants and Children (>3 months): 50 to100 mg/kg/day in equally divided doses every 6 to 8 hours. Use 100 mg/kg/day (not to exceed the maximum adult dose) for more severe or serious infections.
Bone and Joint Infections: 150 mg/kg/day (not to exceed the maximum adult dose) in equally divided doses every 8 hours.
Bacterial meningitis: Initially 200 to 240 mg/kg/day IV in divided doses every 8 hours.
Direction for Reconstitution

Cefuroxime 750 mg intramuscular Injection: Add 3 ml water for injection BP and shake gently for dispersion

For 750 mg intravenous injection: Add 6 ml water for injection BP and shake gently for dispersion.
For 1.5 mg intravenous injection: Add 16 ml water for injection BP and shake gently for dispersion.
For Suspension: shake the bottle well before adding water. Then add 35 ml of boiled and cooled water (with the help of the provided cup from different company) to the bottle. Then continue shaking the bottle until the powder is dissolved property.

Contraindication

Cefuroxime is contraindicated in patients with known allergy to Cephalosporins.

Side Effect

Cefuroxime has been associated with nausea and vomiting in a small number of patients.

Acute Over dosage

Excessively large dosage of all cephalosporins can cause cerebral irritation and may cause convulsions. This complication is unlikely to occur in routine practice unless the patient is in renal failure hemodialysis or peritoneal dialysis can remove Cefuroxime.

Precaution

As with antibiotics, prolonged use of Cefuroxime may result in the over growth of non-susceptible organisms (e.g. Canada enterococci, Clostridium difficult), which may require interruption of treatment.

Use in Pregnancy and Lactation

While all antibiotics should be avoided in the first trimester if possible. Cefuroxime has been safety used in later pregnancy to treat urinary and other infections. The placental transfer of Cefuroxime into the fetus was studied in 20 women and therapeutically active concentrations were found in the serum of infants for up to 6 hours after delivery. Cefuroxime is excreted in human milk and consequently caution should be exercised when Cefuroxime is administered to a nursing mother.

Drug Interaction

No potentially hazardous interactions have been reported.

Storage Condition

Tablet: Store below 30 degree C, protected from light and moisture.
Suspension: Store below 25 degree C, protected from light and moisture.
Injection: Store below 25 degree C, protected from light and moisture. Use reconstituted solution immediately. The reconstituted solution is stable for 2 hours at room temperature and for 12 hours when refrigerated at 2 degree to 8 degree Celsius.

How Supplied from different companies

Cefuroxime 125 mg tablet: Box containing 20 tablets in blister pack.
Cefuroxime 250 mg tablet: Box containing 20 tablets in blister pack.
Cefuroxime 500 mg tablet: Box containing 20 tablets in blister pack.
Cefuroxime powder for suspension (70 ml): Bottle containing 70 ml suspension (after reconstitution).

Cefuroxime 750 mg IM/IV injection: Pack of 1 vial containing Cefuroxime 750 mg as Cefuroxime sodium BP accompanied by a solvent ampoule of 10 ml water for injection. It also contains a complementary pouch comprised of disposable syringe (10 ml) needle, alcohol pad and first aid bandage.

Cefuroxime 1.5 gm IV injection: Pack of 1 vial containing Cefuroxime 1.5 gm as Cefuroxime sodium BP accompanied by two solvent ampoule of 10 ml water for injection in each. It also contains a complementary pouch comprised of disposable syringe (20 ml) needle alcohol pad and first aid bandage.