- Application for Temporary Registration of Pharmacist with Pharmacy Board of Malaysia
- List of Training Premises for Provisionally Registered Pharmacist (PRP)
- Psoriasis Medication Therapy Adherence Clinic (MTAC) Protocol Third Edition
- Obstetrics & Gynaecology Ward Pharmacy Services Protocol
- Thalassaemia Medication Therapy Adherence Clinic (TMTAC) Protocol
You are here
Formulari Ubat KKM (FUKKM)
| # | Generic Name | MDC | Category | Indications | Pres. Restrictions | Dosage |
|---|---|---|---|---|---|---|
| 871 | Lansoprazole 30 mg Tablet | A02BC03000T1001XX | A* | i) Peptic ulcer disease ii) Reflux oesophagitis iii) Zollinger-Ellison Syndrome iv) For eradication of Helicobacter pylori in combination with antibiotic | i) 30mg daily in the morning for up to 4 weeks (duodenal ulcer) or up to 8 weeks (gastric ulcer). Maintenance: 15mg/day. ii) 30mg OD in the morning for up to 8 weeks if not healed. Maintenance: 15mg OD. iii) Initially 60mg OM & adjust as required. Daily doses >120mg should be given in 2 divided doses. iv) 30 mg twice daily in combination with any of the 2 antibiotics (clarithromycin 500 mg twice daily , amoxicillin 1 g twice daily or metronidazole 400 mg twice daily) for 1-2 weeks | |
| 872 | Lanthanum Carbonate 1000mg Chewable Tablet | V03AE03130T2004XX | A* | Phosphate binding agent for the treatment of hyperphosphataemia in dialysis patients with sustained hypercalcaemia of more than three months and secondary hyperparathyroidism | Initial: 750 to 1500 mg/day in divided doses with meals, then titrate in increments of 750 mg/day at intervals of 2 to 3 weeks. Maintenance: 1500-3000 mg/day in divided doses. Max: 3750 g/day | |
| 873 | Laronidase 2.9mg/5ml Injection | A16AB05000P3001XX | A* | Hurler and Hurler-Scheie forms of Mucopolysaccharidosis I (MPS I) and for patients with the Scheie form who have moderate to severe symptoms | 0.58 mg/kg of body weight administered once-weekly as an intravenous infusion | |
| 874 | Latanoprost 0.005% and Timolol Maleate 0.5% eye drops | S01ED51-990-D20-04-XXX | A* | For reduction of Intraocular Pressure (IOP) in patients with Open-angle Glaucoma (OAG) and Ocular Hypertension (OH) who are insufficiently responsive to topical beta-blocker. | None | 1 drop in the affected eye(s) once daily |
| 875 | Latanoprost 0.005% Eye Drops | S01EE01-000-D20-01-XXX | A* | Reduction of elevated intraocular pressure in patients with open-angle glaucoma | None | 1 drop in the affected eye(s) once daily. |
| 876 | Leflunomide 10mg Tablet | L04AA13000T1001XX | A* | i) Persistent active rheumatoid arthritis ii) Active psoriatic arthritis | Loading dose: 100 mg once daily for 3 days. Maintenance: 10-20 mg once daily | |
| 877 | Leflunomide 20mg Tablet | L04AA13000T1002XX | A* | i) Persistent active rheumatoid arthritis ii) Active psoriatic arthritis | Loading dose: 100 mg once daily for 3 days. Maintenance: 10-20 mg once daily. | |
| 878 | Lenalidomide 10 mg Capsule | L04AX04000C1002XX | A* | In combination with dexamethesone is indicated for the treatment of multiple myeloma patients who have received at least one prior therapy | Recommended starting dose: 25 mg once daily on days 1 to 21 of repeated 28 day cycle with dexamethasone 40 mg once daily on days 1 to 4, 9 to 12 and 17 to 20 of each 28 day cycle for the first 4 cycles of therapy, thereafter dexamethasone 40 mg once daily on day 1 to 4 every 28 day cycle | |
| 879 | Lenalidomide 15 mg Capsule | L04AX04000C1003XX | A* | In combination with dexamethesone is indicated for the treatment of multiple myeloma patients who have received at least one prior therapy | Recommended starting dose: 25 mg once daily on days 1 to 21 of repeated 28 day cycle with dexamethasone 40 mg once daily on days 1 to 4, 9 to 12 and 17 to 20 of each 28 day cycle for the first 4 cycles of therapy, thereafter dexamethasone 40 mg once daily on day 1 to 4 every 28 day cycle | |
| 880 | Lenalidomide 25 mg Capsule | L04AX04000C1004XX | A* | In combination with dexamethesone is indicated for the treatment of multiple myeloma patients who have received at least one prior therapy | Recommended starting dose: 25 mg once daily on days 1 to 21 of repeated 28 day cycle with dexamethasone 40 mg once daily on days 1 to 4, 9 to 12 and 17 to 20 of each 28 day cycle for the first 4 cycles of therapy, thereafter dexamethasone 40 mg once daily on day 1 to 4 every 28 day cycle | |
| 881 | Lenalidomide 5 mg Capsule | L04AX04000C1001XX | A* | In combination with dexamethesone is indicated for the treatment of multiple myeloma patients who have received at least one prior therapy | Recommended starting dose: 25 mg once daily on days 1 to 21 of repeated 28 day cycle with dexamethasone 40 mg once daily on days 1 to 4, 9 to 12 and 17 to 20 of each 28 day cycle for the first 4 cycles of therapy, thereafter dexamethasone 40 mg once daily on day 1 to 4 every 28 day cycle | |
| 882 | Lenvatinib 10mg Hard Capsule | L01XE29-196-C11-01-xxx | A* | For the treatment of adult patients with progressive, locally advanced or metastatic, differentiated (papillary/follicular/Hürthle cell) thyroid carcinoma (DTC), refractory to radioactive iodine (RAI). | None | 24mg once daily |
| 883 | Lenvatinib 4mg Hard Capsule | L01EX08-196-C11-01-XXX | A* | i. Indicated as monotherapy for the treatment of adult patients with advanced or unresectable hepatocellular carcinoma (HCC) who have received no prior systemic therapy ii. For the treatment of adult patients with progressive, locally advanced or metastatic, differentiated (papillary/follicular/Hürthle cell) thyroid carcinoma (DTC), refractory to radioactive iodine (RAI). | Indikasi i: Only for patients with Child-Pugh A | Indikasi i: The recommended daily dose of lenvatinib is 8 mg (two 4 mg capsules) once daily for patients with a body weight of < 60 kg and 12 mg (three 4 mg capsules) once daily for patients with a body weight of ≥ 60 kg. Dose adjustments are based only on toxicities observed and not on body weight changes during treatment (Refer package insert for dosage adjustments) Treatment should continue as long as clinical benefit is observed or until unacceptable toxicity occurs. Indikasi ii: 24mg once daily |
| 884 | Letrozole 2.5 mg Tablet | L02BG04000T1001XX | A* | Hormonal therapy in breast cancer in post-menopausal women if failed /contraindicated to Tamoxifen | 2.5 mg once daily | |
| 885 | Leucovorin Calcium (Calcium Folinate) 10mg/mL Injection | V03AF03-237-P30-02-XXX | A | (i) Biochemical modulator for 5-Fluorouracil in the treatment of solid tumour; (ii) As rescue for high dose methotrexate; (iii) Megaloblastic anaemias due to deficiency of folic acid | None | i) 200mg/m2 by slow IV injection over a minimum 3 minutes, followed by 5-Fluorouracil or 20mg/m2 IV followed by 5-Fluorouracil. In both cases, treatment is repeated daily for 5 days; may repeat at 4-week intervals for 2 courses then 4- to 5-week intervals ii) 15 mg (approximately 10mg/m2) every 6 hours for 10 doses, starting 24 hours after the beginning of the methotrexate infusion iii) Up to 1 mg daily Dosing is individualised and according to product insert/protocol |
| 886 | Leucovorin Calcium (Calcium Folinate) 15 mg Tablet | V03AF03-390-T10-01-XXX | A | i) Treatment of folic acid antagonist overdose; ii) Leucovorin (folinic acid) plus tegafur-uracil combination therapy is indicated for the treatment of colorectal cancer in: a) Metastatic stage, b) Adjuvant setting, c) Concurrent setting. | None | i) 15 mg every 6 hours for the next 48 - 72 hours; ii) Metastatic stage: Leucovorin Calcium 30 mg TDS, Day 1-28, rest 7 days for 5 cycles Adjuvant setting: Leucovorin Calcium 30 mg TDS, Day 1-28, rest 7 days for 5 cycles; Concurrent setting: Leucovorin Calcium 25 mg /day, D8- D36, for 4 weeks. Dosing is individualised and according to product insert/protocol |
| 887 | Leuprolide (Leuproreline) Acetate 11.25 mg Injection | L02AE02-122-P50-02-XXX | A* | i) Endometriosis ii) Hormonal therapy in advanced prostate cancer | 11.25 mg every 3 months | |
| 888 | Leuprolide (Leuproreline) Acetate 22.5mg injection | L02AE02-122-P20-01-XXXX | A* | Hormonal therapy in advanced prostate cancer. | 22.5mg SC every 3 months | |
| 889 | Leuprolide (Leuproreline) Acetate 3.75mg Injection | L02AE02-122-P50-01-XXX | A* | i) Endometriosis ii) Hormonal therapy in advanced prostate cancer | None | i) 3.75 mg monthly for 3 - 6 months ii) 3.75 mg IM or SC injection monthly |
| 890 | Leuprolide (Leuproreline) Acetate 45mg Injection | L02AE02-122-P40-01-XXX | A* | Hormonal therapy in advanced prostate cancer | None | 45mg SC every 6 months |
| 891 | Levetiracetam 100 mg/ml Oral Solution | N03AX14-000-L99-01-XXX | A* | As adjunctive therapy in the treatment of partial onset seizures with or without secondary generalization in adults and children from 4 years of age with epilepsy | None | CHILD: 4-11 years and adolescent (12-17 years) less than 50 kg: Initially 10 mg/kg twice daily, may be increased up to 30 mg/kg twice daily. Dose changes should not exceed increments or decrements of 10 mg/kg two times daily twice weekly |
| 892 | Levetiracetam 100mg/ml Injection | N03AX14-000-P30-01-XXX | A* | i) Monotherapy therapy in the treatment of partial onset seizures with or without secondary generalization in patients from age 16 years of age with newly diagnosed epilepsy ii) Adjunctive treatment in partial onset seizures with or without secondary generalization in adults and children from 4 years of age with epilepsy; juvenile myoclonic epilepsy and idiopathic generalized tonic clonic epilepsy from 12 years of age | To be initiated when conventional IV antiepileptic drugs failed to achieve control, or oral form is temporarily not feasible in seizure emergencies | i) ADULTS and ADOLESCENT (from 16 years): Starting dose: 250 mg twice daily, Increase dose to 500 mg twice daily after 2 week. Dose can be further increased by 250 mg twice daily every 2 weeks depending upon the clinical response. Max: 1500 mg twice daily. ii) ADULT more than 18 years and ADOLESCENT (12 to 17 years) more than or equal to 50 kg: Initially 500 mg twice daily may be increased up to 1500 mg twice daily. Dose changes can be made in 500 mg twice daily increments or decrements 2 to 4 weekly. CHILD (4 to 11 years) and ADOLESCENT (12 to 17 years) less than 50 kg : Initially 10 mg/kg twice daily, may be increased up to 30 mg/kg twice daily. Dose changes should not exceed increments or decrements of 10 mg/kg twice daily every 2 weeks. CHILD more than or equal to 50 kg: Adult dose |
| 893 | Levetiracetam 250 mg Tablet | N03AX14-000-T10-01-XXX | A* | i) Monotherapy therapy in the treatment of partial onset seizures with or without secondary generalization in patients from age 16 years of age with newly diagnosed epilepsy ii) Adjunctive treatment in partial onset seizures with or without secondary generalization in adults and children from 4 years of age with epilepsy; juvenile myoclonic epilepsy and idiopathic generalized tonic clonic epilepsy from 12 years of age | i) Monotherapy ADULTS and ADOLESCENT (from 16 years): Starting dose: 250 mg twice daily, Increase dose to 500 mg twice daily after 2 week. Dose can be further increased by 250 mg twice daily every 2 week depending upon the clinical response. Max: 1500 mg twice daily. ii) ADULT more than 18 years and ADOLESCENT (12-17 years) more than or equal to 50 kg: Initially 500 mg twice daily may be increased up to 1500 mg twice daily. Dose changes can be made in 500 mg twice daily increments or decrements 2-4 weekly. CHILD (4-11 years) and ADOLESCENT (12-17 years) less than 50 kg: Initially 10 mg/kg twice daily, may be increased up to 30 mg/kg twice daily. Dose changes should not exceed increments or decrements of 10 mg/kg twice daily every 2 weeks. CHILD more than or equal to 50 kg: Adult dose | |
| 894 | Levetiracetam 500 mg Tablet | N03AX14-000-T10-02-XXX | A* | i) Monotherapy therapy in the treatment of partial onset seizures with or without secondary generalization in patients from age 16 years of age with newly diagnosed epilepsy ii) Adjunctive treatment in partial onset seizures with or without secondary generalization in adults and children from 4 years of age with epilepsy; juvenile myoclonic epilepsy and idiopathic generalized tonic clonic epilepsy from 12 years of age | None | i) Monotherapy ADULTS and ADOLESCENT (from 16 years): Starting dose: 250 mg twice daily, Increase dose to 500 mg twice daily after 2 week. Dose can be further increased by 250 mg twice daily every 2 week depending upon the clinical response. Max: 1500 mg twice daily. ii) ADULT more than 18 years and ADOLESCENT (12-17 years) more than or equal to 50 kg: Initially 500 mg twice daily may be increased up to 1500 mg twice daily. Dose changes can be made in 500 mg twice daily increments or decrements 2-4 weekly. CHILD (4-11 years) and ADOLESCENT (12-17 years) less than 50 kg : Initially 10 mg/kg twice daily, may be increased up to 30 mg/kg twice daily. Dose changes should not exceed increments or decrements of 10 mg/kg twice daily every 2 weeks. CHILD more than or equal to 50 kg: Adult dose |
| 895 | Levobupivacaine 5mg/ml Injection | N01BB10-110-P30-01-XXX | A | Production of local or regional anesthesia for surgery and obstetrics, and for postoperative pain management | None | Surgical anesthesia : Lumber epidural : 10 - 20 ml (50 - 150 mg) , caesarean section : 15 - 30 ml (75 - 150 mg), intrathecal: 3 ml (15 mg), peripheral nerve block : 1 - 40 ml, ilioinguinal/iliohypogastric block. CHILD : 0.25 - 0.5 ml/kg (1.25-2.5 mg/kg) |
| 896 | Levocetirizine Dihydrochloride 5mg Tablet | R06AE09-110-T10-01-XXX | A* | Symptomatic treatment of allergic rhinitis (including persistent allergic rhinitis) and chronic idopathic urticaria | None | Children above 12 years and adults: 5 mg orally once daily (Swallow whole, do not chew/crush). |
| 897 | Levodopa 100 mg and Carbidopa 25 mg Tablet | N04BA02000T1001XX | B | Parkinson's disease | Patients not receiving Levodopa before, initially 100 - 125 mg 3 - 4 times daily adjusted according to response. Maintenance: 0.75 - 2 g in divided doses. In patients previously treated with Levodopa the dose should be about 20 - 25% of the dose previously being taken | |
| 898 | Levodopa 100 mg, Benserazide 25 mg HBS capsule | N04BA02977C1001XX | B | Parkinson's Disease | Initial: 100/25 mg 1-2 times/day, increase every 3-4 days until therapeutic effect, optimal dosage: 400/100 mg to 800/200 mg/day divided into 4-6 doses. Dose: 200/50 mg used only when maintenance therapy is reached and not to exceed levodopa 1000-1200 mg/benserazide 250-300 mg per day | |
| 899 | Levodopa 100mg, Carbidopa 25mg and Entacapone 200mg Tablet | N04BA03977T1002XX | A* | Idiopathic Parkinson's disease | The optimum daily dosage must be determined by careful titration of levodopa in each patient. The daily dose should preferably be optimised using 1 of the 4 available tablet strengths (50/12.5/200mg, 100/25/200mg, 150/37.5/200mg or 200/50/200mg levodopa/carbidopa/entacapone). Patients should be instructed to take only 1 tablet/dose administration. While the experience with total daily dosage >200 mg carbidopa is limited, the maximum recommended daily dose of entacapone is 2000 mg and therefore the maximum dose, for the strengths of 50/12.5/200 mg, 100/25/200 mg and 150/37.5/200 mg, is 10 tablets/day. Ten (10) tablets of the strength 150/37.5/200 mg equals carbidopa 375 mg/day. Therefore, using a maximum recommended daily dose of carbidopa 375 mg, the maximum daily dose of 200/50/200 mg is 7 tablets per day. The maximum total daily levodopa dose administered should not exceed 1500 mg. | |
| 900 | Levodopa 150 mg, Carbidopa 37.5 mg and Entacapone 200 mg Tablet | N04BA03977T1003XX | A* | Idiopathic Parkinson's disease | The optimum daily dosage must be determined by careful titration of levodopa in each patient. The daily dose should preferably be optimised using 1 of the 4 available tablet strengths (50/12.5/200mg, 100/25/200mg, 150/37.5/200mg or 200/50/200mg levodopa/carbidopa/entacapone). Patients should be instructed to take only 1 tablet/dose administration. While the experience with total daily dosage >200 mg carbidopa is limited, the maximum recommended daily dose of entacapone is 2000 mg and therefore the maximum dose, for the strengths of 50/12.5/200 mg, 100/25/200 mg and 150/37.5/200 mg, is 10 tablets/day. Ten (10) tablets of the strength 150/37.5/200 mg equals carbidopa 375 mg/day. Therefore, using a maximum recommended daily dose of carbidopa 375 mg, the maximum daily dose of 200/50/200 mg is 7 tablets per day. The maximum total daily levodopa dose administered should not exceed 1500 mg. |