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Praluent

Praluent

alirocumab

Manufacturer:

sanofi-aventis

Distributor:

DKSH
Concise Prescribing Info
Contents
Alirocumab
Indications/Uses
Adjunct to diet & maximally tolerated statin therapy in adults w/ heterozygous familial hypercholesterolemia or clinical atherosclerotic CV disease who require additional lowering of LDL-C. Established atherosclerotic CV disease in adults to reduce CV risk by lowering LDL-C levels in combination w/ max tolerated statin dose w/ or w/o other lipid-lowering therapies or, alone or in combination w/ other lipid-lowering therapies in patients who are statin-intolerant, or for whom statin is contraindicated.
Dosage/Direction for Use
SC 75 mg once every 2 wk. Alternative starting dose: 300 mg once every 4 wk.
Contraindications
Special Precautions
Not to be inj into active skin disease areas or injury eg, sunburns, skin rashes, inflammation or infections. Discontinue use if serious allergic reactions occur. Severe renal & hepatic impairment. Not recommended during pregnancy & lactation. Childn & adolescents <18 yr.
Adverse Reactions
Local inj site reactions eg, erythema/redness, itching, swelling, pain/tenderness; upper resp tract signs & symptoms eg, oropharyngeal pain, rhinorrhea, sneezing; pruritus.
Drug Interactions
Increased target-mediated clearance & reduced systemic exposure w/ statins & other lipid-modifying therapy.
MIMS Class
Dyslipidaemic Agents
ATC Classification
C10AX14 - alirocumab ; Belongs to the class of other lipid modifying agents.
Presentation/Packing
Form
Praluent soln for inj (pre-filled pen) 150 mg/mL
Packing/Price
1's;2's;6's
Form
Praluent soln for inj (pre-filled pen) 75 mg/mL
Packing/Price
1's;2's;6's
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