Anda di sini
Formulari Ubat KKM (FUKKM)
# | Generic Name | MDC | Category | Indications | Pres. Restrictions | Dosage |
---|---|---|---|---|---|---|
421 | Degarelix 80mg Injection | L02BX02-000-P40-01-002 | A* | Treatment of adult male patients with advanced hormone- dependent prostate cancer. | Patients who are contraindicated to Gonadotrophin Releasing Hormone (GnRH) agonist | 240 mg administered as two consecutive subcutaneous injections of 120 mg each. Maintenance dose* – monthly administration: 80 mg administered as one subcutaneous injection *The first maintenance dose should be given one month after the starting dose. |
422 | Denosumab in 1.0 mL solution (60 mg/mL) Pre‐filled syringe (subcutaneous injection) | M05BX04000P4001XX | A* | Post-Menopausal Osteoporosis. | To be used by Orthopaedic Specialist, Rheumatologist, Endocrinologist and Geriatricians | A single subcutaneous injection of 60 mg administered once every 6 months. Patients should receive calcium and vitamin D supplements whilst undergoing treatment. |
423 | Desferrioxamine B Methanesulphonate 0.5g Injection | V03AC01-196-P30-01-XX | A | i) Acute iron poisoning in children. ii) Investigation and treatment of haemochromatosis. iii) Diagnosis and treatment of aluminium toxicity in patients with renal failure and dialysis iv) Chronic iron toxicity or overload | None | i) 2 g by IM immediately and 5 g by mouth after gastric lavage. ii) 0.5 - 1.5 g by IM injection daily. iii) Diagnosis: 5 mg per kg by slow intravenous infusion during the last hour of haemodialysis. Treatment: 5 mg per kg once a week by slow intravenous infusion during the last hour of dialysis iv) 30 - 50 mg/kg |
424 | Desflurane Liquid | N01AB07000L5001XX | A | i) Induction and maintenance of anaesthesia in adult ii) Maintenance of anaesthesia in infants & children | ADULT: Induction , initially 3% in oxygen or nitrous oxide/oxygen and increased by 0.5%-1% every 2-3 breaths or as tolerated (up to 11%), until loss of consciousness. Maintenance: 2.5%-8.5% with or without concomitant nitrous oxide CHILD: maintenance, inhaled in concentrations of 5.2%-10% with or without concomitant nitrous oxide | |
425 | Desloratadine 2.5mg/5ml syrup | R06AX27-000-L90-01-XXX | A* | Allergic rhinitis and chronic idiopathic urticaria. | For use in children 1-2 years old only. | For children only: 1-5 yrs: 2.5ml once a day (with or without meal) 6-11 yrs: 5ml once a day (with or without meal) |
426 | Desloratadine 5mg Tablet | R06AX27-000-T10-01-XXX | A* | Allergic rhinitis and chronic idiopathic urticaria | None | Adults and Adolescents (12 years of age and older): 5mg once a day regardless of mealtime. |
427 | Desmopressin 0.1 mg Tablet | H01BA02122T1001XX | A | i)Central diabetes insipidus ii)Primary nocturnal enuresis iii)Treatment of nocturia associated with nocturnal polyuria in adult | i)ADULT and CHILD : 0.1-0.2mg 3 times daily, up to 0.1-1.2mg daily ii) ADULT & Child≥5 yr 0.2-0.4mg at night iii)Initially 0.1 mg at night. May be increased to 0.2 mg and then to 0.4 mg by means of weekly increase | |
428 | Desmopressin 0.2 mg Tablet | H01BA02122T1002XX | A | i) Central diabetes insipidus ii) Primary nocturnal enuresis iii)Treatment of nocturia associated with nocturnal polyuria in adult | i)ADULT and CHILD : 0.1-0.2mg 3 times daily, up to 0.1-1.2mg daily ii) ADULT & Child≥5 yr 0.2-0.4mg at night iii)Initially 0.1 mg at night. May be increased to 0.2 mg and then to 0.4 mg by means of weekly increase | |
429 | Desmopressin 100mcg/ml Nasal Spray | H01BA02-122-A41-01-XXX | A | i) Central Diabetes Insipidus ii) Primary nocturnal enuresis | None | i) ADULT : 10 - 20 mcg 1-2 times daily. CHILD: 5 - 10mcg 1-2 times daily ii) 10-40 mcg nocte |
430 | Desmopressin 120mcg Sublingual Tablet | H01BA02-122-T70-02-001 | A | i) Central diabetes insipidus ii) Primary nocturnal enuresis iii) Treatment of nocturia associated with nocturnal polyuria in adults | i) 60mcg 3 times daily sublingually (daily dose range from 120mcg to 720mcg) ii) 120mcg once daily at bedtime, sublingually (maximum dose 240mcg) iii) 60mcg once daily at bedtime (dose range from 120mcg to 240mcg) | |
431 | Desmopressin 60mcg Sublingual Tablet | H01BA02-122-T70-01-001 | A | i) Central diabetes insipidus ii) Primary nocturnal enuresis iii) Treatment of nocturia associated with nocturnal polyuria in adults | i) 60mcg 3 times daily sublingually (daily dose range from 120mcg to 720mcg); ii) 120mcg once daily at bedtime, sublingually (maximum dose 240mcg); iii) 60mcg once daily at bedtime (dose range from 120mcg to 240mcg). | |
432 | Desmopressin Acetate 4mcg/ml Injection | H01BA02-122-P30-01-XXX | A | Central Diabetes Insipidus. | None | Adults 1-4 mcg 1-2 times daily. Children above the age of 1 year 0.4-1 mcg 1-2 times daily. Children below the age of 1 year 0.2-0.4 mcg 1-2 times daily. |
433 | Desogestrel 0.075mg Tablet | G03AC09-000-T10-01-XXX | A* | Contraception. Only for women who should not take combined oral contraceptives (COCs) eg Obese, smoker, migraine, breast feeding | None | Tablets must be taken in the order directed on the package every day at about the same time with some liquid as needed. One tablet is to be taken daily for 28 consecutive days. Each subsequent pack is started immediately after finishing the previous pack. |
434 | Desogestrel 150mcg & Ethinylestradiol 20mcg Tablet | G03AA09-954-T10-02-XX | A/KK | Oral contraception | None | One tablet daily for 21 days starting on 1st day of menses followed by 7 tablet-free days. |
435 | Desogestrel 150mcg & Ethinylestradiol 30mcg Tablet | G03AB05-954-T10-01-XXX | C+ | Contraception | None | 1 tablet daily for 21 days, subsequent courses repeated after 7 day interval (during which withdrawal bleeding occurs) |
436 | Desvenlafaxine 50 mg Extended Release Tablet | N06AX23999T5002XX | A* | Major depression | Recommended dose is 50mg once daily, with or without food. | |
437 | Dexamethasone 0.5mg Tablet | H02AB02-000-T10-01-XXX | A | i) Prophylaxis and management of nausea and vomiting in cancer chemotherapy, post-operation and palliative care ii) Treatment of adrenocortical function abnormalities iii) Any other treatment requiring corticosteroid therapy. | None | 0.5mg to 10mg daily is given for oral administration. Dose can be titrated up to 20mg daily in severe disease depending on the condition being treated. The dosing is individualized according to product insert / protocol |
438 | Dexamethasone 4mg Tablet | H02AB02-000-T10-03-XXX | A | i) Prophylaxis and management of nausea and vomiting in cancer chemotherapy, post-operation and palliative care ii) Treatment of adrenocortical function abnormalities iii) Any other treatment requiring corticosteroid therapy. | None | 0.5mg to 10mg daily is given for oral administration. Dose can be titrated up to 20mg daily in severe disease depending on the condition being treated. The dosing is individualized according to product insert / protocol |
439 | Dexamethasone 700mcg intravitreal implant | S01BA01-000-P11-01-XXX | A* | i) Treatment of adult patients with visual impairment due to diabetic macular oedema (DME) who are pseudophakic. ii) Treatment of adult patients with macular oedema following either Branch Retinal Vein Occlusion (BRVO) or Central Retinal Vein Occlusion (CRVO) | For indication (ii): a) First line therapy for patient with contraindication to anti-VEGF treatment. b) Second line therapy for patient refractory to anti-VEGF treatment. c) To be prescribed by Ophthalmologist only | Indication (i): The recommended dose is one dexamethasone intravitreal implant to be administered to the affected eye. Administration to both eyes concurrently is not recommended. Patients treated with dexamethasone intravitreal implant who have experienced an initial response and in the physician’s opinion may benefit from retreatment without being exposed to significant risk should be considered for retreatment. Retreatment may be performed after approximately 6 months if the patient experiences decreased vision and/or an increase in retinal thickness, secondary to recurrent or worsening diabetic macular oedema. There is currently no experience of the efficacy or safety of repeat administrations in DME beyond 7 implants. Indication (ii): 700 mcg injected intravitreally into one affected eye. Administration to both eyes concurrently is not recommended. Repeat doses at 6 months interval should be considered when a patient experiences a response to treatment followed subsequently by a loss in visual acuity. |
440 | Dexamethasone and Neomycin Sulphate and Polymyxin B Eye Ointment | S01CA01-990-G51-01-XXX | A | Treatment of ocular inflammation when concurrent use of an antimicrobial is judged necessary | None | Apply a small amount into the conjunctival sac(s) 3 – 4 times daily, may be used adjunctively with drops at bedtime |
441 | Dexamethasone and Neomycin Sulphate and Polymyxin B Sulphate Ophthalmic Suspension | S01CA01-990-D20-01-XXX | A | Treatment of ocular inflammation when concurrent use of an antimicrobial is judged necessary | None | 1 - 2 drops hourly for severe cases and 4 - 6 hourly for mild infection |
442 | Dexamethasone Sodium Phosphate 0.1% Eye Drops | S01BA01-162-D20-01-XXX | A | Acute steroid responsive inflammatory and allergic conditions | None | 1 - 2 drops 4 - 6 times a day |
443 | Dexamethasone Sodium Phosphate 4 mg/ml Injection | H02AB02-162-P30-01-XXX | B | i) Prophylaxis and management of nausea and vomiting in cancer chemotherapy, post-operation and palliative care ii) Treatment of adrenocortical function abnormalities iii) Any other treatment requiring corticosteroid therapy. | None | i-iii) Initial dosage: 0.5 mg to 20 mg per day depending on the specific disease entity being treated. The total daily dosage should not exceed 80 mg. The dosing is individualized according to product insert / protocol |
444 | Dexlansoprazole 30 mg delayed release capsule | A02BC06-000-C30-01-XXX | A* | i) Treatment of erosive esophagitis (EE); ii) Maintenance of healed erosive esophagitis (EE); iii) Symptomatic treatment of non-erosive gastroesophageal reflux disease. | As a second-line therapy for: i) Patients with refractory EE; ii) Geriatrics; iii) Patients with polypharmacy. | i) Treatment of EE – 60 mg once daily for 8 weeks; ii) Maintenance of healed EE – 30 mg once daily for 6 months; iii) Symptomatic non-erosive gastroesophageal reflux disease – 30 mg once daily for 4 weeks. |
445 | Dexlansoprazole 60 mg delayed release capsule | A02BC06-000-C30-02-XXX | A* | i) Treatment of erosive esophagitis (EE); ii) Maintenance of healed erosive esophagitis (EE); iii) Symptomatic treatment of non-erosive gastroesophageal reflux disease. | As a second-line therapy for: i) Patients with refractory EE; ii) Geriatrics; iii) Patients with polypharmacy. | i) Treatment of EE – 60 mg once daily for 8 weeks; ii) Maintenance of healed EE – 30 mg once daily for 6 months; iii) Symptomatic non-erosive gastroesophageal reflux disease – 30 mg once daily for 4 weeks. |
446 | Dexmedetomidine HCl 100mcg/ml Injection | N05CM18-110-P40-01-XXX | A* | i) Sedation of intubated and mechanically ventilated ICU patients. ii) For use only by specialist anaesthetist: For sedation of non-intubated patients prior to and/or during surgical and other procedures | None | i) Not to be infused for more than 24 hours, 1 mcg/kg over 10 minutes as loading dose. Maintenance dose: 0.2 - 0.7 mcg/kg/hr ii) Not to be infused for more than 24 hours, 1 mcg/kg over 10 minutes as loading dose. Maintenance dose: 0.2 - 0.7 mcg/kg/hr |
447 | Dextrose 10% Injection | B05BA03000P6002XX | B | For parenteral replenishment of fluid and minimal carbohydrate calories as required by the clinical condition of the patient | According to the needs of the patient | |
448 | Dextrose 20% Injection | B05BA03000P6003XX | B | For parenteral replenishment of fluid and minimal carbohydrate calories as required by the clinical condition of the patient | According to the needs of the patient | |
449 | Dextrose 30% Injection | B05BA03000P3004XX | B | For parenteral replenishment of fluid and minimal carbohydrate calories as required by the clinical condition of the patient | According to the needs of the patient | |
450 | Dextrose 5% Injection | B05BA03000P6001XX | B | For parenteral replenishment of fluid and minimal carbohydrate calories as required by the clinical condition of the patient | According to the needs of the patient |