LEQVIO284 mg/1.5 ml

LEQVIO 284 mg/1.5 ml is a sc injection manufactured by Nevian Lifescience PLC in Bangladesh. Its active ingredient is Inclisiran.

Indications

LEQVIO is a small interfering RNA (siRNA) directed to proprotein convertase subtilisin kexin type 9 (PCSK9) mRNA indicated as an adjunct to diet and exercise to reduce low-density lipoprotein cholesterol (LDL-C) in:

adults with hypercholesterolemia.

adults and pediatric patients aged 12 years and older with heterozygous familial hypercholesterolemia (HeFH).

pediatric patients aged 12 years and older with homozygous familial hypercholesterolemia (HoFH).

Contraindications

Prior serious hypersensitivity to inclisiran or any of the excipients in Inclisiran.

Pharmacology

Inclisiran is a double-stranded small interfering ribonucleic acid (siRNA), conjugated on the sense strand with triantennary N-Acetylgalactosamine (GalNAc) to facilitate uptake by hepatocytes. In hepatocytes, inclisiran utilizes the RNA interference mechanism and directs catalytic breakdown of mRNA for PCSK9. This increases LDL-C receptor recycling and expression on the hepatocyte cell surface, which increases LDL-C uptake and lowers LDL-C levels in the circulation.

Dosage & Administration

The recommended dosage of Inclisiran for adults and pediatric patients aged 12 years and older is 284 mg administered as a single subcutaneous injection initially, again at 3 months, and then every 6 months.

If a planned dose is missed by less than 3 months, administer Inclisiran and maintain dosing according to the patient’s original schedule.

If a planned dose is missed by more than 3 months, restart with a new dosing schedule - administer Inclisiran initially, again at 3 months, and then every 6 months.

Assess LDL-C when clinically indicated. The LDL-lowering effect of Inclisiran may be measured as early as 30 days after initiation and anytime thereafter without regard to timing of the dose.

Side Effects

Common adverse reactions in clinical trials (≥ 3%): injection site reaction, arthralgia, and bronchitis.

Pregnancy & Lactation

Advise pregnant patients and patients who can become pregnant of the potential risk to a fetus. Advise patients to inform their healthcare provider of a known or suspected pregnancy to discuss if Inclisiran should be discontinued. There is no information on the presence of inclisiran in human milk, the effects on the breastfed infant, or the effects on milk production. Inclisiran was present in the milk of lactating rats in all dose groups.

Precautions & Warnings

Hypersensitivity Reactions: Have been reported in patients treated with LEQVIO. Advise patients on the signs and symptoms of hypersensitivity reactions and instruct patients to seek medical attention promptly.

Therapeutic Class

Other Anti-anginal & Anti-ischaemic drugs

Storage Conditions

Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.

Disclaimer: This information is for reference only. Always consult a registered physician before taking any medicine.