Your dose will depend on bacteria causing the infection.
Description.
In patients with severe liver impairment (n=4), although there was a 76% increase in the half-life (5.9 and 10.4 days for normal and impaired patients, respectively) of the active enantiomer of bicalutamide no dosage adjustment is necessary Casodex® (bicalutamide) 50 mg tablets for oral administration.Casodex is contraindicated in any patient who has shown a hypersensitivity reaction to the drug or any of the tablet’s components.
https://www.mims.com/indonesia/drug/info/cravit-cravit%20iv/?type=brief MIMS. Obat ini mengandung antibiotik yaitu , selain itu dapat digunakan untuk mengobati infeksi pada organ prostat (prostatitis bakterial kronik), infeksi kulit, infeksi saluran kemih dengan komplikasi, infeksi ginjal (pielonefritis akut).½ - 1 tablet sebanyak 1 kali/hari diberikan selama 7-14 hari sesuai dengan petunjuk dokterDapat dikonsumsi sebelum makan atau bersamaan dengan waktu makan.Hipersensitif terhadap levofloxacin dan obat antibiotik jenis quinolone lain, penderita epilepsi, riwayat gangguan jaringan ikat pada otot (tendon), ibu hamil,menyusui, anak-anak dan remaja.Cukupi asupan air putih ketika meminum obat ini, hati-hati pada penderita gangguan ginjal, gangguan sistem saraf pusat, gangguan fungsi hati, pasien dengan riwayat kejang, lansia diatas 60 tahun, sedang dalam pengobatan sterod, riwayat gangguan mental dan penderita kencing manis.Obat anti-inflamasi non steroid, obat-obatan diabetes, obat TBC (mycobacterium tuberculosis), wafarin, theophylline, obat anti-inflamasi non-steroid, obat-obatan antidiabetes, tablet besi, suplemen zinc, antasida, didanosine atau sucralfate. Co-administration of bicalutamide with food has no clinically significant effect on rate or extent of absorption.Bicalutamide undergoes stereospecific metabolism. However, the half-life of the R-enantiomer was increased approximately 76% (5.9 and 10.4 days for normal and impaired patients, respectively) in patients with severe liver disease (n=4).Renal impairment (as measured by creatinine clearance) had no significant effect on the elimination of total bicalutamide or the active R-enantiomer.Long-term clinical trials have been conducted with dosages up to 200 mg of Casodex daily and these dosages have been well tolerated. Cravit merupakan obat keras dan harus dengan resep dokter. Table 2 shows descriptive data for growth rates for the overall population and for subgroups defined by history of previous treatment for testotoxicosis with ketoconazole, spironolactone, anastrozole or other aromatase inhibitors.Total testosterone concentrations increased by a mean of 5 mmol/L over the 12 months of treatment from a baseline mean of 10 mmol/L. General supportive care, including frequent monitoring of vital signs and close observation of the patient, is indicated.Casodex® (bicalutamide) tablets contain 50 mg of bicalutamide, a non-steroidal androgen receptor inhibitor with no other known endocrine activity. If clinical symptoms or signs suggestive of liver dysfunction occur (e.g., nausea, vomiting, abdominal pain, fatigue, anorexia, “flu-like” symptoms, dark urine, jaundice, or right upper quadrant tenderness), the serum transaminases, in particular the serum ALT, should be measured immediately. Adverse reactions considered possibly related to bicalutamide by investigators included gynecomastia (6/14, 43%), central precocious puberty (2/14, 14%), breast tenderness (2/14, 14%), breast pain (1/14, 7%), asthenia (1/14, 7%), increased alanine aminotransferase [ALT] (1/14, 7%), increased aspartate aminotransferase [AST] (1/14, 7%), and musculoskeletal chest pain (1/14, 7%). Six of the 12 patients started treatment at an estradiol concentration below the level of quantification.There were no deaths, serious adverse events, or discontinuations due to adverse events during the study. Kondisi ini dapat disebabkan oleh berbagai hal, mulai dari hidung yang kering, alergi, iritasi, ataupun masalah lain. The hazard ratio for time to death (survival) was 0.87 (95% confidence interval 0.72 to 1.05).There was no significant difference in time to objective tumor progression between treatment groups (see Figure 2).
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