Voxamin XR Capsule (Extended Release) 100 mg Uses, Dosage, Side Effects and more
Voxamin XR Capsule (Extended Release) 100 mg Uses, Dosage, Side Effects, Food Interaction and all others data.
Trade Name | Voxamin XR Capsule (Extended Release) 100 mg |
Generic | Fluvoxamine Maleate |
Weight | 100 mg |
Type | Capsule (Extended Release) |
Therapeutic Class | SSRIs & related anti-depressant drugs |
Manufacturer | Renata Limited |
Available Country | Bangladesh |
Last Updated: | January 7, 2025 at 1:49 am |
Uses
Maprotiline Hydrochloride is indicated in- Obsessive-Compulsive Disorder Depressive illness Panic Disorder Eating Disorders Chronic Tension HeadacheDosage
Voxamin XR Capsule (Extended Release) 100 mg dosage
Adults: The recommended starting dose for Voxamin XR Capsule (Extended Release) 100 mg Tablets in adult patients is 50 mg, administered as a single daily dose at bedtime. In the controlled clinical trials establishing the effectiveness of Voxamin XR Capsule (Extended Release) 100 mg Tablets in OCD, patients were titrated within a dose range of 100 to 300 mg/day. Consequently, the dose should be increased in 50 mg increments every 4 to 7 days, as tolerated, until the maximum therapeutic benefit is achieved, not to exceed 300 mg per day. It is advisable that a total daily dose of more than 100 mg should be given in two divided doses. If the doses are not equal, the larger dose should be given at bedtime.Pediatric Population (children and adolescents): The recommended starting dose for Voxamin XR Capsule (Extended Release) 100 mg Tablets in pediatric populations (ages 8-17 years) is 25 mg, administered as a single daily dose at bedtime. In a controlled clinical trial establishing the effectiveness of Voxamin XR Capsule (Extended Release) 100 mg Tablets in OCD, pediatric patients (ages 8-17) were titrated within a dose range of 50 to 200 mg/day. Physicians should consider age and gender differences when dosing pediatric patients. The maximum dose in children up to age 11 should not exceed 200 mg/day. Therapeutic effects in female children may be achieved with lower doses. Dose adjustment in adolescents (up to the adult maximum dose of 300 mg) may be indicated to achieve therapeutic benefit. The dose should be increased in 25 mg increments every 4 to 7 days, as tolerated until the maximum therapeutic benefit is achieved. It is advisable that a total daily dose of more than 50 mg should be given in two divided doses. If the two divided doses are not equal, the larger dose should be given at bedtime.Elderly or Hepatically Impaired Patients: Elderly patients and those with hepatic impairment have been observed to have a decreased clearance of fluvoxamine maleate. Consequently, it may be appropriate to modify the initial dose and the subsequent dose titration for these patient groups.