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Parmodia

Parmodia

Manufacturer:

Kowa

Distributor:

DKSH
Concise Prescribing Info
Contents
Pemafibrate
Indications/Uses
Adjunctive therapy to diet or exercise to reduce triglycerides & increase HDL-C levels in patients w/ dyslipidemia characterised by high triglyceride ≥150 mg/dL w/ associated risk eg, HTN & smoking.
Dosage/Direction for Use
Adult Usual dose: 0.1 mg bd. Max: 0.2 mg bd. Renal impairment Max: 0.2 mg daily.
Administration
May be taken with or without food.
Contraindications
Hypersensitivity. Cholelithiasis. Concomitant use w/ cyclosporine or rifampicin. Severe hepatic disorder, Child-Pugh grade B or C cirrhosis, or biliary obstruction. Pregnancy.
Special Precautions
Discontinue use if diffuse myalgia, myositis, muscle cramps & weakness &/or marked increased creatine kinase (>5 x ULN) is present. History of cholelithiasis; preexisting muscular disease. Periodically monitor liver & renal function. Concomitant use w/ HMG-CoA reductase inhibitors. Hepatic disorder (Child-Pugh grade A cirrhosis). Renal impairment. Avoid use during lactation. Low birth wt infants, newborns, infants & childn. Elderly.
Adverse Reactions
Cholelithiasis; DM; increased blood creatine phosphokinase.
Drug Interactions
Muscle toxicity w/ HMG-CoA reductase inhibitors eg, pravastatin Na, simvastatin, fluvastatin Na. Increased plasma conc w/ clopidogrel sulfate, clarithromycin, HIV PIs (eg, ritonavir), fluconazole. Decreased plasma conc w/ anion exchange resins eg, cholestyramine, colestimide; strong CYP3A inducers eg, carbamazepine, phenobarb, phenytoin, foods containing Hypericum perforatum (St. John's wort).
MIMS Class
Dyslipidaemic Agents
ATC Classification
C10AB12 - pemafibrate ; Belongs to the class of fibrates. Used in the treatment of hyperlipidemia.
Presentation/Packing
Form
Parmodia FC tab 0.1 mg
Packing/Price
10 × 10's
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