Země: Spojené státy
Jazyk: angličtina
Zdroj: NLM (National Library of Medicine)
ALISKIREN HEMIFUMARATE (UNII: C8A0P8G029) (ALISKIREN - UNII:502FWN4Q32)
Avera McKennan Hospital
ALISKIREN HEMIFUMARATE
ALISKIREN 150 mg
PRESCRIPTION DRUG
New Drug Application
TEKTURNA- ALISKIREN HEMIFUMARATE TABLET, FILM COATED AVERA MCKENNAN HOSPITAL ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE TEKTURNA SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR TEKTURNA. TEKTURNA (ALISKIREN) TABLETS, FOR ORAL USE INITIAL U.S. APPROVAL: 2007 WARNING: FETAL TOXICITY _SEE FULL PRESCRIBING INFORMATION FOR COMPLETE BOXED WARNING._ WHEN PREGNANCY IS DETECTED, DISCONTINUE TEKTURNA AS SOON AS POSSIBLE. (5.1) DRUGS THAT ACT DIRECTLY ON THE RENIN-ANGIOTENSIN SYSTEM CAN CAUSE INJURY AND DEATH TO THE DEVELOPING FETUS. (5.1) RECENT MAJOR CHANGES Contraindications (4) 3/2015 Warnings and Precautions (5.2, 5.5) 3/2015 INDICATIONS AND USAGE Tekturna is a renin inhibitor (RI) indicated for: The treatment of hypertension, to lower blood pressure (1.1) Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions . DOSAGE AND ADMINISTRATION Starting dose: 150 mg once daily with a routine pattern with regard to meals. If blood pressure remains uncontrolled titrate up to 300 mg daily. (2.1, 2.2) Majority of effect of given dose attained in 2 weeks (2.1) DOSAGE FORMS AND STRENGTHS Tablets: 150 mg, 300 mg (3) CONTRAINDICATIONS Do not use with angiotensin receptor blockers (ARBs) or angiotensin-converting enzyme inhibitors (ACEIs) in patients with diabetes. (4) Hypersensitivity to any of the components. (4) WARNINGS AND PRECAUTIONS Avoid concomitant use with ARBs or ACEIs particularly in patients with renal impairment [creatinine clearance (CrCl) <60 mL/min]. (5.2, 5.4) Anaphylactic Reactions and Angioedema. (5.3) Hypotension: Correct imbalances in volume and/or salt depleted patients. (5.4) Impaired Renal Function: Monitor serum creatinine periodically. (5.5) Hyperkalemia: Monitor potassium levels periodically. (5.6) ADVERSE REACTIONS Most common adverse reaction: diarrhea (incidence 2.3%) (6.1) TO REPORT SUSPECTED ADVERSE REACTIONS, CONTACT NOVARTIS PHARMACEUTICALS C Přečtěte si celý dokument