
Ocarnix330 mg
Incepta Pharmaceuticals Ltd.
Levocarnitine is indicated for conditions related to carnitine deficiency.
Levocarnitine is indicated for conditions related to carnitine deficiency. Its uses are classified below by strength of evidence.
Levocarnitine should be used for these adjunct or off-label purposes only under a physician's guidance, as evidence is more limited than for the approved indications.
Dosage of Levocarnitine is individualized according to the indication, patient age, body weight, and clinical response. General guidance is summarized below; a physician's specific prescription should always be followed.
| Indication | Typical Adult Dose | Typical Pediatric Dose |
|---|---|---|
| Primary carnitine deficiency (oral) | 990 mg to 3 g of Levocarnitine per day, in 2-3 divided doses | 50-100 mg/kg/day of Levocarnitine in divided doses, up to a maximum of 3 g/day |
| Acute metabolic crisis (IV) | Loading dose of about 50 mg/kg of Levocarnitine by slow IV infusion, followed by 50 mg/kg/day of Levocarnitine in divided doses | Similar weight-based dosing under specialist supervision |
| Carnitine deficiency in dialysis patients (IV) | 10-20 mg/kg of Levocarnitine (based on dry body weight) given intravenously after each haemodialysis session | Not routinely established; individualized by nephrologist |
Oral Levocarnitine may be taken with or without food; taking it with food may reduce a fishy body odor some patients notice. Intravenous Levocarnitine must be administered by slow infusion as directed by a healthcare professional; do not administer by rapid IV push.
Levocarnitine is generally well tolerated. Reported side effects include:
Levocarnitine is contraindicated only in patients with known hypersensitivity to Levocarnitine or to any excipient in the specific formulation used. There are no other well-established absolute contraindications to Levocarnitine.
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