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Contents |
Orlistat |
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Indications |
In conjunction with dietary modification in the management of obesity i.e. in
patients with BMI ≥25 kg/m2. Also, in patients with BMI ≥23 kg/m2
if there are associated risk factors e.g. hypercholesterolemia,
HTN and cardiovascular diseases. |
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Dosage |
1 cap tid. |
|
Administration |
Should be taken with food (Take immediately before or during or up to 1 hr after each main meal.
If a meal is missed or contains no fat, the dose may be omitted.). |
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Contraindications |
If taking cyclosporine. Chronic malabsorption syndrome or cholestasis; gallbladder problems;
undergone organ transplant; allergic reaction w/ orlistat. |
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Special Precautions |
Diabetic patients. Fat-soluble vit may be necessary during long-term therapy,
but should be taken at least 2 hr before or after an orlistat dose or at bed time.
Pregnancy & lactation. Childn <18 yr. |
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Adverse Drug Reactions |
GI disturbances eg fecal incontinence, flatulence, fatty stools or discharge. |
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Pregnancy Category (US FDA) |
Category B: Either animal-reproduction studies have not demonstrated a foetal
risk but there are no controlled studies in pregnant women or animal-reproduction
studies have shown an adverse effect (other than a decrease in fertility) that was
not confirmed in controlled studies in women in the 1st trimester
(and there is no evidence of a risk in later trimesters). |
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ATC Classification |
A08AB01 - Orlistat ; Belongs to the class of peripherally
acting antiobesity products. Used in the treatment of obesity. |
|
Poison Schedule |
Non-Rx |