Dosage of Losaric in details
Losaric Dosage
Generic name: Losaric 25mg
Dosage form: tablet, film coated
The information at Drugs.com is not a substitute for medical advice. Always consult your doctor or pharmacist.
Hypertension
Adult Hypertension
The usual starting dose of Losaric is 50 mg once daily. The dosage can be increased to a maximum dose of 100 mg once daily as needed to control blood pressure. A starting dose of 25 mg is recommended for patients with possible intravascular depletion (e.g., on diuretic therapy).
Pediatric Hypertension
The usual recommended starting dose is 0.7 mg per kg once daily (up to 50 mg total) administered as a tablet or a suspension. Dosage should be adjusted according to blood pressure response. Doses above 1.4 mg per kg (or in excess of 100 mg) daily have not been studied in pediatric patients.
Losaric is not recommended in pediatric patients less than 6 years of age or in pediatric patients with estimated glomerular filtration rate less than 30 mL/min/1.73 m2.
Hypertensive Patients with Left Ventricular Hypertrophy
The usual starting dose is 50 mg of Losaric once daily. Hydrochlorothiazide 12.5 mg daily should be added and/or the dose of Losaric should be increased to 100 mg once daily followed by an increase in hydrochlorothiazide to 25 mg once daily based on blood pressure response.
Nephropathy in Type 2 Diabetic Patients
The usual starting dose is 50 mg once daily. The dose should be increased to 100 mg once daily based on blood pressure response.
Dosage Modifications in Patients with Hepatic Impairment
In patients with mild-to-moderate hepatic impairment the recommended starting dose of Losaric is 25 mg once daily. Losaric has not been studied in patients with severe hepatic impairment.
Preparation of Suspension (for 200 mL of a 2.5 mg/mL suspension)
Add 10 mL of Purified Water USP to an 8 ounce (240 mL) amber polyethylene terephthalate (PET) bottle containing ten 50 mg Losaric tablets. Immediately shake for at least 2 minutes. Let the concentrate stand for 1 hour and then shake for 1 minute to disperse the tablet contents. Separately prepare a 50/50 volumetric mixture of Ora-Plus™ and Ora-Sweet SF™. Add 190 mL of the 50/50 Ora-Plus™/Ora-Sweet SF™ mixture to the tablet and water slurry in the PET bottle and shake for 1 minute to disperse the ingredients. The suspension should be refrigerated at 2-8°C (36-46°F) and can be stored for up to 4 weeks. Shake the suspension prior to each use and return promptly to the refrigerator.
More about Losaric (Losaric)
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Consumer resources
- Losaric
- Losaric (Advanced Reading)
Professional resources
- Losaric (AHFS Monograph)
- Losaric (FDA)
Related treatment guides
- Diabetic Kidney Disease
- High Blood Pressure
What other drugs will affect Losaric?
Tell your doctor about all medicines you use, and those you start or stop using during your treatment with Losaric, especially:
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a diuretic or "water pill";
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other blood pressure medications;
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lithium;
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celecoxib; or
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aspirin or other NSAIDs (non-steroidal anti-inflammatory drugs) such as ibuprofen (Advil, Motrin), naproxen (Aleve), celecoxib, diclofenac, indomethacin, meloxicam, and others.
This list is not complete. Other drugs may interact with Losaric, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide.
Losaric interactions
No significant drug-drug pharmacokinetic interactions have been found in interaction studies with hydrochlorothiazide, digoxin, warfarin, cimetidine and phenobarbital. Rifampin, an inducer of drug metabolism, decreased the concentrations of Losaric and its active metabolite. In humans, 2 inhibitors of CYP450 3A4 have been studied. Ketoconazole did not affect the conversion of Losaric to the active metabolite after IV administration of Losaric, and erythromycin had no clinically significant effect after oral administration. Fluconazole, an inhibitor of CYP450 2C9, decreased active metabolite concentration and increased Losaric concentration. The pharmacodynamic consequences of concomitant use of Losaric and inhibitors of CYP450 2C9 have not been examined. Subjects who do not metaolize Losaric to active metabolite have been shown to have a specific, rare defect in CYP450 2C9. These data suggest that the conversion of Losaric to its active metabolite is mediated primarily by CYP450 2C9 and not CYP450 3A4.
No difference in exposure was found with concomitant treatment with fluvastatin (weak inhibitor of CYP2C9).
As with other drugs that block angiotensin II or its effects, concomitant use of potassium-sparing diuretics (eg, spironolactone, triamterene, amiloride), drugs which may increase potassium levels (heparin), potassium supplements or salt substitutes containing potassium may lead to increases in serum potassium. Co-medication is not advisable.
Lithium: As with other drugs which affect the excretion of sodium, lithium excretion may be reduced. Therefore, serum lithium levels should be monitored carefully if lithium salts are to be co-administered with angiotensin II receptor antagonists.
Nonsteroidal Anti-Inflammatory Drugs (NSAIDs) Including Selective Cyclooxygenase-2 (COX-2) Inhibitors: In some patients with compromised renal function who are being treated with NSAIDs including those that selectively inhibit COX-2 inhibitors, the co-administration of angiotensin II receptor antagonists including Losaric may result to a further deterioration of renal function. These effects are usually reversible.
Reports suggest that NSAIDs including COX-2 inhibitors may diminish the antihypertensive effect of angiotensin II receptor antagonists, including Losaric. This interaction should be given consideration in patients taking NSAIDs including selective COX-2 inhibitors concomitantly with angiotensin II receptor antagonists.
The combination should be administered with caution, especially in the elderly. Patients should be adequately hydrated and consideration should be given to monitoring renal function after initiation of concomitant therapy and periodically thereafter.
References
- DailyMed. "LOSARTAN POTASSIUM: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
- FDA/SPL Indexing Data. "JMS50MPO89: The UNique Ingredient Identifier (UNII) is an alphanumeric substance identifier from the joint FDA/USP Substance Registration System (SRS).". https://www.fda.gov/ForIndustry/Data... (accessed September 17, 2018).
- MeSH. "Antihypertensive Agents". https://www.ncbi.nlm.nih.gov/mesh/68... (accessed September 17, 2018).
Reviews
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Information checked by Dr. Sachin Kumar, MD Pharmacology